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To read CCHR’s Declaration of Mental Health Rights click here. CCHR International is a non-profit mental health watchdog, responsible for helping to enact more than 150 laws protecting individuals from abusive or coercive psychiatric practices. CCHR has long fought against forced drugging and electroshocking of patients, involuntary commitment, the psychiatric drugging of children, & psychiatric incarceration of political dissidents. CCHR has also been the primary mental health watchdog seeking to enact informed consent into the field of mental health – a practice which is virtually non-existent in the psychiatric/mental health industry. To read about CCHR’s accomplishments click here.
http://www.cchrint.org/
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50 Years Ago Thomas Szasz Rocked The World of Psychiatry: The Difference Between A Disease and a Disorder
By Dr. Jeffrey Schaler
Assistant Professor of Justice, Law & Society
March, 2010
It is fifty years now since Thomas Szasz rocked the world of psychiatry by writing The Myth of Mental Illness: Foundations of a Theory of Personal Conduct. His work continues to have a profound impact on how we think about disease, behavior, liberty, justice, responsibility, and most important of all, what it means to be human. Szasz has shown us how the idea of mental illness is used by the state to deprive innocent people of freedom, and guilty persons of justice. Without the state involved, the medicalization of behavior means nothing.
He has shown us how the idea of mental illness functions as legal fiction within our legal system. In this sense, the idea of mental illness has been used much as the idea that African American slaves were considered three-fifths of a person. Persons labeled as mentally ill are now considered three-fifths of a person. It is as if there was a postscript at the bottom of the Bill of Rights that reads: “PS: For mentally healthy people only.”
The courts will not allow the idea of mental illness to be disproved, in much the same way that the idea that slaves could be three-fifths person was not allowed to be disproved. Today, mental illness as legal fiction maintains the institution of psychiatric slavery.
Mental illness diagnoses have more to do with politics and science fiction, than medicine and science. Take for example the idea that people with a homosexual orientation are mentally ill. The category was excluded from the Diagnostic and Statistical Manual of Mental Disorders – our contemporary “Malleus Maleficorum,” or “Hammer of Witches” – the same way it was included, for political reasons, not scientific reasons. No one discovered that homosexuality was a disease, and no one discovered that it isn’t a disease. They pronounced it as such, in each case, because of political pressure.
About two years after The Myth of Mental Illness was first published, Szasz published another book that has had an equally profound impact on freedom and responsibility. In Law, Liberty and Psychiatry he predicted the following:
“Although we may not know it, we have, in our day, witnessed the birth of the Therapeutic State. This is perhaps the major implication of psychiatry as an institution of social control.”
Thomas Szasz wrote that in 1963.
We live in a Therapeutic State today. Moral management now masquerades as medicine. The state dictates a “duty to be healthy.”
Seventy years ago another state, Nazi Germany, dictated a “duty to be healthy.” Back then, murder masqueraded as medicine. I think you all know what I’m referring to. We don’t need a weatherman to know which way the wind blows.
Today, good health practices have become a social responsibility. Bad health practices are viewed as socially irresponsible behavior. When health and illness are applied to the mind and behavior, this means that people must think and speak and act the right way. Otherwise, they may end up in a prison called a mental hospital.
I am one of the few college professors in the United States, if not in the world, who teaches Szasz’s ideas on a regular basis in college. And in every course, my students have always said at least two things to me: This stuff by Szasz is changing my life. And why hasn’t anyone ever taught his work in class before?
Because professors are punished for teaching Szasz; they can lose their jobs if they do so. I know. I have the scars to prove it. If you read my book, Szasz Under Fire, you will see how the same thing almost happened to Thomas Szasz. He came a hair away from being fired for teaching Thomas Szasz!
The Myth of Mental Illness and the subsequent Law, Liberty and Psychiatry are not so unsophisticated as to deny the existence of behaviors that people find disturbing. Quite to the contrary, Szasz’s writings clarify the difference between behavior and disease, description and explanations for behavior, and the consequences of labeling behavior as a disease within the arenas of law, medicine, social and public policy.
Szasz has simply pointed out what pathologists have always known: A disease refers to cellular pathology. Period. A behavior cannot be a disease. And he has also fought endlessly for the rights of persons labeled mentally ill. He will be ninety years old on April 15. He is still writing one book after another. He writes books faster than I can read them!
He has also shown us how behavior is strategic, the expression of what philosophers call moral agency. Today’s neuroscientists, psychiatrists and clinical psychologists have attempted to reduce man to the category of things. They deny the existence of moral agency. Let me give you one simple example of how this is so.
Conventional wisdom, particularly as it appears in the media, leads people to believe that brains cause behavior, as if the brain could act. Psychiatrists and the neuroscientists they aspire emulate, regard man as a machine, an incredibly complicated machine, but a machine nevertheless. Everything that is human is ultimately reducible to electrical and chemical interactions.
This is especially so when it comes to socially unacceptable, abnormal, disturbing and criminal behavior. Bad brains are said to cause bad behavior. Bad brains, in this, sense refers to problems in the structure and function of the brain.
Now if bad brains cause bad behavior, it only follows that good brains must cause good behavior. In other words, brains that work correctly, brains that are structurally and functionally healthy, cause good and admirable behaviors.
While psychiatrists try to excuse bad behaviors by ultimately blaming bad brains, they inadvertently (or perhaps intentionally) are removing personal responsibility for the good things that people do. When someone commits a heroic deed, for example, shows courage, compassion, and care for others at great personal expense and with great risk of danger, the person is then not choosing to do what is clearly important to do.
The brain, according to this way of thinking, is causing the person to do this good thing, in the same way that a bad brain causes someone to prey on others. There is no need to praise someone for his altruism, heroism, and courage, his brain made him do it.
Some psychiatrists have equated human behavior with seizure activity: An alcoholic reaching for that drink too many is having an epileptic seizure. So is the mother sacrificing her own life for the life of her child.
What is left of the person, if this is so? What is left of the person if brains cause bad and good behavior? What is that represented by the pronoun “I?” What happens to moral agency?
Nothing. From this way of thinking, human beings are reduced to the category of things. Things do not choose, they are caused. Things do not feel. Things are not alive. Things have no conscience, no values, no morality, no ethics. And most important, things do not care, for self or others.
This is the legacy of psychiatry and neuroscience today, when it comes to entertaining biological explanations for behavior. Mind is equated with brain, behavior with disease, good with bad, morality with medicine, and ethics with mechanics. In other words, there is no soul. That which we consider uniquely human is destroyed by psychiatry and neuroscience.
How does this fit into law? Through a simple equation. Liberty and responsibility are two sides of the same coin. If we increase one, we increase the other. If we decrease one, we decrease the other. The more free man is, the more responsible he must be. The more responsible man is, the more he is captain of his own ship.
What institutional psychiatry as an extension of the state would have us believe is this: The more we decrease responsibility, the more we increase freedom. In other words, the more you allow us to be in charge of your life, the more you abdicate responsibility, the more you embrace the paternalism we say is good for you, the more you will be free. For obedience to authority is the greatest political virtue.
What then must we do? Szasz has done his job, what is ours? I believe our job is this: We get psychiatry out of the courthouse. We do not need to destroy psychiatry. It will destroy itself if we sever its invisible umbilical cord to the mother-state. Once psychiatry is available to people by choice only, it will die a natural death. Very few people will seek out psychiatrists if they cannot hire and fire them at will.
Psychiatrists know this. That is why they are so afraid of Thomas Szasz.
And that is why they are so afraid of those who understand what I am saying here. As I tell my students every semester, “don’t believe a word I say. Just think about it and come to your own conclusion.” That kind of independence and autonomy scares institutional psychiatrists and those who run the therapeutic state.
It should.
Jeffrey A. Schaler is an assistant professor of justice, law, and society at American University’s School of Public Affairs in Washington, D.C. Professor Schaler’s work is focused on the “therapeutic state”—the union of medicine and state. He completed his doctoral and master’s degrees in human development at the University of Maryland College Park, where the major emphasis of his research was addiction and social policy. Dr. Schaler is particularly interested in how research in the behavioral sciences is interpreted and applied in public, social, and legal policy arenas. He writes and speaks extensively on the relationship between liberty and responsibility.
Dr. Thomas Szasz is a Professor of Psychiatry Emeritus, State University of New York. He is a well known critic of the moral and scientific foundations of psychiatry and has authored more than 30 books on the subject including the Manufacture of Madness, The Myth of Mental Illness and The Therapeutic State. He is the co-founder of the Citizens Commission on Human Rights (CCHR) and has said of the organization, “We should all honor CCHR because it is really the organization that for the first time in human history has organized a politically, socially, internationally significant voice to combat psychiatry. This has never been done in human history before.”
Related Posts
- The Psychopharmaceutical Industrial Complex—creating epidemic of mental illness through psychiatry’s chemical imbalance hoax (0)
- “ADHD is a total 100% fraud. The millions of schoolchildren around the world being drugged have no disease” – Neurologist (4)
- An exceptional article from psychiatrist Peter Breggin: Huffington Post – Our Psychiatric Civilization (2)
- The New American: Psychiatry Enters Dangerous Territory—Newly proposed disorders and the threat to personal liberty (0)
- The Huffington Post— Creating Disease: Big Pharma and Disease Mongering (0)
Our U.S. Military: Betrayed and Drugged
“Psychiatrists under contract with the Veteran Affairs—in my opinion—are legal drug dealers who almost took my life.”
- Former Marine Scout Sniper
By Shane Ellison
Award-winning scientist, Masters Degree in Organic Chemistry
March 31, 2010
Chad was a Marine Scout Sniper who served two tours in Iraq. Upon being honorably discharged as a Sgt. in 2007, he summoned the courage to ask for help in dealing with the images and emotions that gnawed on him from being dropped into combat. Like so many of his peers, the help he was given was “meds.” Although Chad was used to putting his life at risk, he never expected that his life would be more directly threatened by the “treatment” he was offered—psychiatric drugs.
After a single day of “following doctor’s orders,” Chad felt things were starting to look up. He seemed to be more cognizant, and the weight of daily struggles was lifted. But, as he describes it, things “quickly flip-flopped.”
“As time passed, I began changing into someone I wasn’t. Once a focused, motivated sniper, my reaction time became stagnant. My thought process became dry and lethargic, while my independence drifted. I became unable to make decisions on my own and reluctantly found myself relying on others in ways I had never done before. I had become a sort of medicated drone. All emotion turned into apathy and I found myself lackadaisical and eventually felt meaningless. That’s where it got really bad for me, and it’s hard to talk about now…. It was as if my brain chemistry went whack.”
This bleak scenario is becoming all too common for today’s military. The psychiatric death threat is becoming riskier than combat. In 2010, Time magazine reported that, “During the month of January, more soldiers committed suicide than were killed by enemy fire in Afghanistan and Iraq combined.” Mystified by the death toll among troops, Army Chief of Staff George Casey said that, “The fact of the matter is, we just don’t know why suicides have increased.”
A group of U.S. Senators have finally raised concern that the use of antidepressants and other prescription drugs are on the rise in the military, particularly among troops in Iraq and Afghanistan. The U.S. FDA has warned these drugs can cause worsening depression, mania, psychosis, suicidal and homicidal ideation. Senator Jim Webb, D-Va., who led the recent Senate Armed Services Committee’s hearing in Washington, said the apparent increase in prescription drugs is “on its face, pretty astounding and troubling.” In fact, Department of Defense statistics show that from 2005 to 2008, there was a 400 percent increase in the prescription of antidepressants and other drugs used to treat anxiety. And a 2007 Army report showed that about 12 percent of combat troops in Iraq and 17 percent of those in Afghanistan were taking antidepressants or sleeping pills.
The suicide trend is not inexplicable, and must be highlighted if troops like Chad are to be saved from the psychiatric death threat. Like the loss of power to a car that results from a broken fuse, mental circuitry is shut off with each and every dose of psychiatric medication. The latest cloning techniques and laboratory methods show this to be the result of “neurotransmitter hijacking,” which scrambles brain circuitry, leaving users like Chad feeling “dry and lethargic,” in times of deep emotional turmoil.
Once neurotransmitter hijacking takes place, users become fully under the spell of psychiatry. The brain can become so scrambled that all normal reality and reason are overwritten by a new confusing and violent agenda. A new personality arises—one with homicidal and suicidal tendencies. Commenting on the biochemical fiasco, CNN publicized that, “Antidepressant drugs actually create a perilous brain imbalance.” Chad barely escaped.
“Rebounding on and off the drugs, I reached the darkest point in my life, strangely enough at home. I packed up my ghillie suit—the same thing I used to camouflage myself as a sniper in enemy territory—and hiked into the wilderness late at night, where no one would find me. I held my .45 cal pistol while attempting the unspeakable…many things raced through my mind, and at the forefront were feelings of worthlessness and my inability to relate to anyone, even myself. As a combat decorated Marine, it’s not something I’m proud of. But it’s a reality that seems to be more common among my peers, and it’s scary as hell.… To this day, I’m not sure what stopped me, probably an act of God. I walked backed vowing to reclaim my life – with everything I had. And, since my mental health declined so drastically since getting on the meds, I felt that getting off them was the first place to start.”
No doubt, combat leads to emotional stress beyond what the rest of us can concede. Listening to the combat experience of Chad paints painful images in my own mind. It’s no wonder indelible scars are left on the minds of our troops. And rather than help them cope, they are literally being drugged to death in a large-scale experiment that goes ignored. Former military psychiatrist, Dr. Grace Jackson, substantiated this stating that, “It’s really a large-scale experiment. We are experimenting with changing people’s cognition and behavior.”
Once off the drugs, Chad’s escape came from getting back to basics—really basic. He starts each day with rigorous exercise and ends it with a deep sleep, induced by L-tryptophan and valerian. His diet is fortified with whey isolate twice per day with meals that consist of unprocessed foods. Sugar and alcohol have been reduced to an absolute minimum. Sauna treatments are regular, and real therapy comes from writing and talking to others who share his experience, as well as giving back in the form of support. He knows his story is only “one of thousands” and that other veterans need help.
Today, Chad has earned his bachelor’s degree—with honors—in a record 2.5 years. At the same time, he founded a Veterans center, which serves as a hub at his Alma Mater to offer support in all matters that relate to being a vet. And when he can, he helps others heed his warning about the military death threat: “Psychiatrists under contract with the Veteran Affairs—in my opinion—are legal drug dealers who almost took my life.”
Shane Ellison is the bestselling author of Over-The-Counter Natural Cures and holds a masters degree in drug design (organic chemistry). He is a two-time recipient of the prestigious Howard Hughes Medical Institute Research Grant for his studies in biochemistry and physiology.
For international drug regulatory warnings about psychiatric drugs causing violence and suicide go to:
http://www.cchrint.org/psychdrugdangers/
For more by Shane Ellison, go to:
http://www.cchrint.org/videos/experts/shane-ellison/
For more information on the current U.S. Senate investigation into this topic see related posts below.
Related Posts
- “Drugged Warriors: Sharp Rise in U.S. Military Psychiatric Drug Use and Suicides” by Psychologist Bruce Levine (1)
- Memorial Day 2010: Psychiatric drugs triggering deaths of U.S. soldiers treated for PTSD (0)
- Earth Times: Neurologist Fred Baughman—Vets Sudden Deaths Due to Antidepressant & Antipsychotic Drugs (2)
- More U.S. Senators voice alarm over 400% increase in psychiatric drugging of troops & increased military suicides (1)
- Senator Calls for Probe of Military Suicides & Antidepressant Use citing 400% increase in psych drug prescriptions (2)
Meet the Psychiatrist Pushing For A Brave New World of Pre-Drugging Kids—Patrick McGorry
By CCHR International
May 21, 2010
One of the most controversial proposed disorders for the upcoming revision of psychiatry’s billing bible of mental disorders, (the DSM-5) is Psychosis Risk Syndrome (PRS) a “mental disorder” that, if voted into DSM, would confirm the allegations that psychiatry is manufacturing a Brave New World for itself—heavily backed by Big Pharma—of drugging children before they develop a “mental illness.” Already criticized for the millions of children being needlessly drugged and the lack of scientific criteria to substantiate any mental diagnosis as a legitimate medical condition, some psychiatrists now want the power to pull out their crystal ball and predict the onset of a psychosis and drug it before it has even occurred. And perhaps the strongest proponent is Australian psychiatrist Patrick McGorry.
Even psychiatrist Allen Frances, former chairman of the previous DSM task force expressed alarm over the proposed diagnosis and its repercussions should it be legitimized, stating, PRS “stands out as the most ill-conceived and potentially harmful.” The Syndrome fails badly on all 3 counts, he says:
“1. It would misidentify many teenagers who are not really at risk for psychosis;
2. The treatment they would most often receive (atypical antipsychotic medication) has no proven efficacy; but,
3. It does have definite dangerous complications.”
Frances adds: “Drug company marketing would influence parents and clinicians to be especially alert to any strangeness in teenagers.” False positives could be as high as 70-90 percent.[i] This can only lead to greater numbers of children and adolescents being harmfully drugged—already one of the major criticisms against psychiatry and a point of contention among many psychiatrists today.
Australian psychiatrist Patrick McGorry, speaking at the APA convention in New Orleans, as a cheerleader for “early intervention” (i.e. pre-drugging) is undeterred. Despite the unpredictability and risk of the drugs prescribed to treat PRS, McGorry wants to go full steam ahead, increasing the number of children being placed on extremely dangerous and even lethal drugs. It should come as no surprise that McGorry is a paid consultant for, and has received speaker’s fees from AstraZenecca, Janssen-Cilag, Eli Lilly, Novartis, Sanofi, Bristol Myers Squibb and Pfizer.[ii]
The theory of PRS wasn’t McGorry’s. He credits Dr. Ewen Cameron, the Canadian psychiatrist who became infamous in the 1980s after it was revealed he had performed cruel and brain-damaging experiments on his patients in the 1950s and 1960s with funding from the CIA.[iii] However, McGorry tested it in a world-first trial. Another study he conducted in 2002 was funded with an unrestricted grant from Janssen-Cilag and supported by pharmaceutical company-funded groups NARSAD and the Stanley Foundation, as well as several Australian agencies. McGorry and colleagues predictably found that risperidone (Risperdal)—made by Janssen—reduced the risk of “transition to psychosis” in young people.[iv] Risperdal has been linked to Type 2 diabetes.
- In Australia, McGorry’s Early Psychosis Prevention and Intervention Center’s (EPPIC) preventive treatment center for young people, PACE, receives drug company funding from Janssen-Cilag. Much of the policy development embodied in the Australian Clinical Guidelines has come out of EPPIC research programs. As Richard Gosden, Ph.D., a highly respected Australian author and academic stated: “This may have paid off handsomely for the company…. It may not be coincidental that a half page of the Clinical Guidelines is dedicated to dosage recommendations for using risperidone in first-episode psychosis. The Clinical Guidelines do not extend these dosage recommendations to include other schizophrenia drugs and the recommendations for risperidone give the appearance of an official endorsement of the drug.” [v]
McGorry’s theory has psychiatry’s skeptics and even psychiatrists aghast:
- One respected American research group equated the practice of pre-drugging children to “performing mastectomies on women who are at risk of—but do not have—breast cancer.” [vi]
- Honorary Professor Anthony Pelosi from the Department of Psychiatry, Hairmyres Hospital, East Kilbride, stated, “So far, evidence from randomized trials does not support the use of psychological therapies or drugs as preventive interventions.”[vii] Further, “After teachers, college counselors, and families were encouraged to refer young people with possibly prodromal [early] symptoms directly to the same clinic for the same care plans…almost 90% were receiving unnecessary ‘preventive’ interventions.” [viii]
- Fellow Australian psychiatrist Niall McLaren says the diagnostic criteria for PRS “has no scientific validity whatsoever…it can never be reliable and…will have huge unforeseen consequences.” Essentially, it means “putting large numbers of teenagers and young adults under the long-term supervision and control of psychiatrists” and that “supervision” includes the “aggressive, indefinite prescription of antipsychotic drugs.” It is the “clearest example I know of pseudoscience. Not since [lobotomies] has psychiatry stumbled so far from the principle of Primum, non nocere. First, do no harm.” [ix]
- Dr. Richard Warner, professor of psychiatry at the University of Colorado, counters the idea that science drives McGorry’s pre-disorder assessment, stating that the screening instrument he uses “is not that accurate in routine use.” Further, “McGorry speculates that a variety of interventions may be effective in preventing schizophrenia in high-risk cases…. Given the expected number of false positives, the potential for harm is significant,” stated Dr. Warner. [x]
- Dr. Jerald Block, a US psychiatrist writing in Bioethics Forum, reported that “preventive pharmacology” (which McGorry, et al. practice) is “ethically questionable territory” because the treatments given “frequently have side effects and complications” and “you are potentially harming people.” The symptoms used to identify them as at risk of schizophrenia are “also remarkably common…adolescence is a period of life that is normally marked by tumultuous changes in personality.” [xi]
- Melissa Raven, psychiatric epidemiologist and policy analyst, adjunct lecturer in Public Health at Flinders University, South Australia, and David Webb, board member of the World Network of Users and Survivors of Psychiatry and working with the research/policy office with the Australia Federation of Disability Organizations, were published last month, writing: “McGorry’s campaign is part of a wider push to promote the medicalization of mental health (for which psychosocial wellbeing is a better term).” “Further doubts must be raised about McGorry’s agenda when you see the substantial funding his organization (Orygen Youth Health) receives from the pharmaceutical industry and also from the US Stanley Foundation, which is notorious for its particularly aggressive approach to the detention and mandatory treatment of people labeled with psychiatric disorders.” He has “personally received funding from many manufacturers of antipsychotics, frequently reports no conflicts of interest, particularly in his many recent Medical Journal of Australia articles, including a supplement on early intervention that repeatedly advocates the use of antipsychotics.” [xii]
Psychosis Risk Syndrome is nothing more than psychiatrists with conflicts of interest drumming up more business at the risk of teenage lives, while increasing the profits for the pharmaceutical industry they serve.
[i] Allen Frances, M.D., “DSM5 ‘Psychosis Risk Syndrome’–Far Too Risky,” Psychology Today, http://www.psychologytoday.com/blog/dsm5-in-distress/201003/dsm5-psychosis-risk-syndrome-far-too-risky.
[ii] http://www.mhanet.ca/documents/2008/Research-Colloquium/0920%20-%20Keynote%20MCGORRY.pdf; http://www.bmj.com/cgi/content/full/337/aug04_1/a695.
[iii] Richard Gosden, Ph.D., “Pre-Psychotic Treatment for Schizophrenia: Preventive Medicine, Social Control, or Drug Marketing Strategy?” Ethical Human Sciences and Services, Vol 1, No. 2, Summer 1999, pp. 165-177, http://sites.google.com/site/richardgosden/ehss.
[iv] Arch Gen Psychiatry, Vol 59, Oct. 2002, http://www.meb.uni-bonn.de/psychiatrie/zebb/literatur/mcgorry.pdf.
[v] Richard Gosden, Ph.D., “Pre-Psychotic Treatment for Schizophrenia: Preventive Medicine, Social Control, or Drug Marketing Strategy?” Ethical Human Sciences and Services, Vol 1, No. 2, Summer 1999, pp. 165-177, http://sites.google.com/site/richardgosden/ehss.
[vi] http://www.ministryoflies.com/pdf-articles/Yale-Lilly.pdf.
[vii] Anthony Pelosi, “Head to Head, Is early intervention in the major psychiatric disorders justified? No,” BMJ 2008;337:a710, http://www.bmj.com/cgi/content/full/337/aug04_1/a710.
[viii] http://www.bmj.com/cgi/content/full/337/aug04_1/a710.
[ix] Niall McLaren, M.D., “Psychosis Risk Syndrome (PRS),” 14 May 2010 (soon to be published).
[x] Richard Warner, MB, DPM, is director of Colorado Recovery in Boulder, Colorado, and professor of psychiatry at the University of Colorado, “Early intervention in psychosis: Future or fad?” Centre for Addiction and Mental Health website, http://www.camh.net/Publications/Cross_Currents/Winter_2007-08/futureorfad_crcuwinter0708.html.
[xi] http://www.ahrp.org/cms/index2.php?option=com_content&do_pdf=1&id=386; http://ww.bioethicsforum.org/ethics-of-preventive-psychopharmacologic-treatments.asp.
[xii] David Webb, Melissa Raven, “McGorry’s ‘early intervention’ in mental health: a prescription for disaster,” Online Opinion, http://www.onlineopinion.com.au/view.asp?article=10267.
Related Posts
- Australian Psychiatrist Patrick McGorry Wants His Pre-Drugging Agenda to Go Global (6)
- Pharma Backed Australian of the Year Psychiatrist Wants Millions in Government Funding for Brave New World of “Pre-Drugging” Kids (18)
- Australian Psychiatrist Patrick McGorry’s push for psychiatric “early intervention” called “a prescription for disaster” (3)
- New York Magazine: Shrink Revolt—The controversy over psychiatric diagnoses and the DSM continues (0)
- Australian of the Year, psychiatrist Patrick McGorry’s pre drugging agenda comes under fire from fellow psychiatrist (1)
DSM Panel Members Still Getting Pharma Funds
Despite promises to cut back on Pharma funds, 56% of DSM V panel members have reported industry ties— Zero improvement over the percent of DSM-IV members.

By CCHR International
May 21, 2010
Due to Senate investigations into the American Psychiatric Association, psychiatrists have promised to cut back on their conflicts of interest (pharma funds), but of the current DSM task force members, those who will be deciding on the holy grail of psychiatric disorders (DSM) and what constitutes a “mental illness” are still heavily funded by Pharma. In fact, there is no improvement over cutting down the number of panel members who are getting paid by industry over the last DSM revision in 1994. It was 56% then and its 56% now. So much for psychiatry’s promises…
Former APA president Nada Stotland stated: “We are in the midst of a revolution caused by public and legislative concern about the influence of the for-profit sector….” [Emphasis added] Part of that public pressure for the APA to disclose its conflicts of interest with pharmaceutical companies was driven by Lisa Cosgrove Ph.D. et al’s study of DSM-IV and DSM-IV-TR committee members, which found that of the 170 members, 56% had one or more financial associations with companies in the pharmaceutical industry. Pharma’s psychotropic drug profits have soared commensurately with the increased numbers of disorders voted into the DSM.
- Of the 137 DSM-V panel members who have posted disclosure statements, 56% have reported industry ties—no improvement over the percent of DSM-IV members.
- Writing in Psychiatric Times (March 6, 2010), Cosgrove and Harold J. Bursztajn, MD, stated: “Although the APA recently announced that it would phase out the visibly industry-supported educational programs, the organization has remained curiously silent about acknowledging and monitoring industry funding of the 2 philanthropic arms of the APA—the American Psychiatric Foundation (APF) and the American Psychiatric Institute for Research and Education (APIRE).”
- APF’s 15-member board of directors includes 4 high-level executives from pharmaceutical companies that either manufacture drugs recommended by APA (i.e.; in APA’s Clinical Practice Guidelines [CPG]) or have products in development targeted for mental disorders.
- Other board members include 2 more with industry ties and a senior vice president at one of the largest public relations agencies in the world, whose clients include 6 drug companies.
- APF’s corporate advisory council comprises pharmaceutical companies that contribute significant funding to APF and manufacture drugs recommended in the APA’s CPG; 6 of the companies give $40,000 “and above” per year.
- APIRE, like APF, does not require disclosure of financial conflicts of interests, yet 9 of 16 of its board members have industry ties.
- At least a quarter of the presenters at this year’s APA congress have significant pharmaceutical company ties.
The APA should sever all ties to pharmaceutical company interests. The US Senate Finance Committee has investigated at least a dozen APA psychiatrists over their undisclosed financial ties to drug companies, including:
Investigated - Alan Schatzberg, APA President: Owned $6 million equity in and as co-founder of drug developer Corcept Therapeutics while principle investigator in an NIH-funded, Stanford-based study of Corcept’s drug mifepristone. Schatzberg initiated the patent application on mifepristone to “treat psychotic depression” in 1997. In 2008, after months of Congressional scrutiny, Schatzberg stepped down from his position as principal investigator in the study.
Investigated – Joseph Biederman: Chief of the Program in Pediatric Psychopharmacology, Massachusetts General Hospital, he earned $1.6 million in consulting fees from drug makers between 2000 and 2007, most of which was not disclosed to Harvard University officials. In March 2009, court documents showed Biederman promised Johnson & Johnson in advance that his studies of their antipsychotic Risperidone would prove effective when used on preschool age children.
Investigated - Melissa DelBello: Research psychiatrist, University of Cincinnati failed to disclose all her Pharma earnings. In 2002, she was the lead author of a study that reported patients benefited from Seroquel by AstraZeneca, which paid her $180,000. She disclosed receiving $100,000 from the company between 2005 and 2007, but federal investigators discovered it was more than double that—$238,000.
Investigated - Frederick Goodwin: Former NIMH director, Goodwin earned at least $1.3 million between 2000 and 2007 for marketing lectures to physicians on behalf of drug makers, which he did not reveal to the producers of “The Infinite Mind” that he hosted on the National Public Radio during its 10-year run. NPR removed the program.
Investigated - Charles Nemeroff: Perhaps the most egregious case exposed was that of Dr. Nemeroff, chair of Emory University’s department of psychiatry and, along with Schatzberg, coeditor of the influential Textbook of Psychopharmacology. He received more than $960,000 from GSK, but reported to Emory $35,000. He earned a further $2.8 million from various drug makers but failed to report at least $1.2 million. Nemeroff resigned his position at Emory in 2008.
Investigated - Martin Keller: Professor of Psychiatry at Brown University. His (and others’) Study 329 (ghostwritten by a GSK rep.) on Paxil use in children allegedly misrepresented data and suppressed information linking Paxil to suicidal tendencies. Keller didn’t disclose the full extent of his financial ties with companies to medical journals that published his research. In another matter, following a criminal investigation, Brown University returned $300,170 to the state of Massachusetts for research Keller’s department never performed. Keller stepped down as chair of psychiatry at Brown.
Investigated - Augustus John Rush: Former Vice-Chairman of the Dept. of Clinical Sciences at the University of Texas Southwestern Medical Center. He reported only $3,000 of the nearly $18,000 that Eli Lilly paid him in 2001. Between 2000 and 2007, he failed to report another $12,000 from various drug companies.
Investigated - Karen Wagner: Professor, University of Texas Medical Branch failed to disclose more than $160,000 in payments from GSK, reporting only $18,000. Wagner worked on NIH-funded studies on the use of Paxil to treat teen depression and was a co-researcher on Study 329 (see Keller), for which she was paid more than $18,000. In 2002, Eli Lily paid her over $11,000, which was not disclosed.
Investigated – Thomas Spencer: Assistant Director of the Pediatric Psychopharmacology Unit at Massachusetts General Hospital and Associate Professor of Psychiatry, Harvard Medical School, reportedly failed to disclose at least $1 million in earnings from drug companies between 2000 and 2007.
Investigated - Timothy Wilens: Associate Professor of Psychiatry at Harvard Medical School allegedly failed to report he had earned at least $1.6 million from drug makers.
Related Posts
- American Psychiatric Association Called Upon to Cut Drug Company Ties and Put Lives of Children Before Profits (5)
- Psychiatrists And Pharma: Undue Influence? Concern about corruption increasing… (1)
- Psychiatric Times – Let’s Call the Whole Thing Off (0)
- The Troubling Link Between Big Pharma and the American Psychiatric Association (0)
- How Pharma funded psychiatrists pathologize behavior as mental illness so more drugs can be marketed to the masses (0)
Australian Psychiatrist Patrick McGorry Wants His Pre-Drugging Agenda to Go Global
“Australia is a place that can actually change the world in mental health, provided we get the right government support to do so.” — Patrick McGorry
By CCHR International
June 16, 2010
A Public Service Announcement on Australian TV features Australian of the Year, psychiatrist Patrick McGorry, claiming that nearly half the population will experience mental ill-health during their lifetime. Considering that after World War II, psychiatrists claimed that one in 20 people had a mental disorder, and now it’s every second one of us, that’s a damning 1000 percent failure rate for psychiatrists in reducing “mental illness.” Let’s get real; the reason psychiatrists claim more people are mentally ill is because they can keep inventing new ways to label them mentally ill—but the press and governments are starting to catch on, evidenced by all the controversy surrounding psychiatry’s upcoming edition of their Diagnostic and Statistical Manual of Mental Disorders (DSM)—better known as psychiatry’s billing bible. Yet of all the proposed “mental disorders” ranging from overeating to kids throwing tantrums, no proposed model of mental disorder is more insidious and dangerous than that of Patrick McGorry, who promotes diagnosing people before they develop a so-called mental disorder—drugging them before they become “mentally ill.” Yet the Australian government has bought into it hook, line and sinker—despite the fact McGorry’s plan is so outrageous, even his peers, such as psychiatrist Allen Frances, former Chair of the DSM task force, have called it ”the most ill-conceived and potentially harmful.”
Make no mistake, the pre-drugging agenda is Patrick McGorry’s baby—his dream for a new paradigm in mental health, one that has the power to diagnose and drug people before they become mentally ill—welcome to the Brave New World of Patrick McGorry. And he isn’t stopping with Australia; his plan is to go global. As he recently stated, “Australia is a place that can actually change the world in mental health, provided we get the right government support to do so.”[1]
The fact that McGorry’s agenda is so controversial—it even has other psychiatrists protesting it—has not deterred the Australian government from funding this “ill-conceived” plan. A recent letter to Citizens Commission on Human Rights states, “The Australian Government is providing $25.5 million over four years from 2010-2011 to expand Early Psychosis Prevention and Intervention Centre (EPPIC) model,” developed by McGorry who founded EPPIC and the Orygen Youth Health in Victoria, Australia.
The Australian Government has already been criticized for massive expenditure on psychotropic drugs increasing more than 660 percent during the last decade—with a whopping 3,100 percent increase on antipsychotic drugs (with at least 15 Australian deaths in the under 19 year olds as a tragic consequence of this). This can only get worse when under McGorry’s plan, with an enormous client base that can be prescribed drugs despite the fact they are not yet “mentally ill.” It’s called prodrome (prodromos meaning the forerunner of an event)—referring to “a period of prepsychotic disturbance” that may or may not develop into psychosis or “schizophrenia”[2]—in other words, the crystal ball theory.
Australia Meets the US in Pre-Drug Scam
McGorry’s plan for Australia to “lead the change” in world mental health is happening—to the detriment of those who may be forced to undergo drug treatment based on a psychiatrist’s hunch that they might, one day, become ill. In the U.S., on May 13, 2009, the Department of Health and Human Services convened a Technical Expert Panel (TEP) discussed “emerging evidence around psychopharmacological interventions for first episode schizophrenia” citing the research efforts of McGorry and others.[3]
The push for pre-diagnosing and pre-drugging has even those within the psychiatric profession calling foul; Dr. Richard Warner, professor of psychiatry at the University of Colorado, counters the idea that science drives McGorry’s pre-disorder assessment, stating, “Given the expected number of false positives, the potential for harm is significant.”[4]
However, as Anthony Pelosi, honorary professor, Department of Psychiatry, Hairmyres Hospital, wrote in a counter to McGorry in the British Medical Journal last year, “this has not stopped their skillful lobbying of politicians, journalists, patients, and carers with upbeat messages about the prevention.”
“Skillful lobbying” is right.
In 2006 McGorry and other researchers, including psychiatrist Michael Berk, Karen Hallam, Craig McNeil, Linda Kaler and psychologist Melissa Hasty reported in the Medical Journal of Australia, “Evidence increasingly indicates that earlier identification may allow for appropriate pharmacological and psychosocial treatments….”[5]
Could they have a Pharma incentive behind this agenda? Berk is financially linked to AstraZeneca, Bristol-Myers Squibb, Eli Lilly, GlaxoSmithKline, Janssen-Cilag, Lundbeck, Organon, Novartis, Mayne Pharma, Servier, Sanofi-Synthelabo, Solvay, and Wyeth and Pfizer.[6] Hallam disclosed received speaker fees from Janssen-Cilag; McNeil received consultancy fees, speaker fees and travel assistance from Eli Lilly, Janssen-Cilag and Sanofi-Aventis; and Hasty and Linda received financial assistance to attend conferences from or Janssen-Cilag, maker of the antipsychotic Risperdal (resperidone).[7]
McGorry has received grant support from Eli Lilly, Janssen-Cilag, Bristol Myers Squibb, Astra-Zeneca, Pfizer, and Novartis.[8] He is a paid consultant for, and has received speaker’s fees from all or most of these companies.[9] Studies published in the British Medical Journal in 2005 and 2008 declared McGorry’s “early intervention studies have received partial support in the form of investigator-initiated unrestricted research grants from Janssen-Cilag.”[10]
The U.S. has already begun adopting the “early intervention” fad, which looks more like a trade in children’s lives and a business opportunity for increased pharmaceutical sales. In March 2010, the Department of Health & Human Services Substance Abuse & Mental Health Service Administration Center for Mental Health Services announced $16.5 million in funding for “Mental Health Transformation Grants,” including the “Early Detection and Intervention for the Prevention of Psychosis Program (EDIPPP).”[11]
EDIPP is the American sister of McGorry’s EPPIC. It was originally bankrolled by a $14.4 million grant from the Robert Wood Johnson Foundation. According to investigative journalist Evelyn Pringle, “The founder of RWJF, Robert Wood Johnson, was chairman of Johnson & Johnson for over 30 years, from 1932 to 1963, as a member of the drug maker’s founding family. Throughout the years, the majority of the Foundation’s money has come from investments in J&J stock.”
In an article in Behavioral Healthcare, in 2008, the Mid-Valley Behavioral Care Network (MVBCN), an intergovernmental Medicaid government insurance-managed healthcare organization situated in Oregon, was recommended to study EPPIC used at Orygen and EDIPPP.
Based on EDIPP and EPPIC, the MVBCN developed the Early Assessment and Support Team (EAST) in 2001. In 2003, the Oregon state legislature allocated $4.3 million to disseminate early psychosis intervention statewide. By March the following year, new programs had begun in 12 counties.[12]
EDIPPP also replicates the “Portland Identification and Early Referral,” or “PIER,” a treatment research program at the Main Medical Center, in Portland, Maine.[13] People typically are referred to PIER by high school guidance counselors, pediatricians, or other clinicians who attended presentations about PIER’s work, says Pringle. “Virtually every person entering the PIER program is prescribed antipsychotics, such as Risperdal or Invega, marketed by Johnson & Johnson,” she added.
Both PIER and EDIPPP are promoted in McGorry’s 2002 book, Implementing Early Intervention in Psychosis: A Guide to Establishing Early Psychosis Services.”[14] The book’s foreword is written by Dr. Jeffrey Lieberman, Professor of Psychiatry, Chairman Department of Psychiatry, Columbia University College of Physicians and Surgeons.[15] Lieberman has taken consulting fees and research grant support from AstraZeneca, Bristol-Myers Squibb, Upjohn Pharmacia, Novartis, Eli Lilly, Janssen, Pfizer, Hoechst AG, & AstraZeneca. He’s on the Speakers Bureaus for Astra Zeneca, Janssen, Eli Lilly and Pfizer.[16]
Lieberman is also the Vice President (North America) of the McGorry instigated group International Early Psychosis Association (IEPA), which was officially incorporated in Victoria in 1998.[17] McGorry is currently Treasurer of the Association.[18] Lieberman is a member of the psychiatric-pharmaceutical company front groups, National Alliance for the Mentally Ill (NAMI) and National Alliance for Research on Schizophrenia and Depression (NARSAD).
Between 1999 and 2003 IEPA received unrestricted education grants from Janssen-Cilag and AstraZeneca.[19] EIPA’s conferences are supported by Janssen-Cilag, AstraZeneca, Eli Lilly, and Bristol-Myers Squibb.[20]
The IEPA lists the “who’s who” of Pre-Psychosis Risk Syndrome (the official label given pre-psychotic symptoms) and many of its board or members disclose manufacturers of antipsychotics as companies they’ve received financing from.
On July 29-30, the First international Youth Mental Health Conference is being held in Melbourne, with keynote speakers, including McGorry. The conference is described by one advocate as an “important and innovative event, attracting the best in the business/industry to discuss the emerging issues of youth mental health.”[21]
It couldn’t have been more adequately stated: business and industry. Herein you see McGorry’s pitch again that Australia is a global leader in this latest psychiatric fad. His invitation online states, “This is an important event for Australia and the mental health field. We expect this to be the first of many similar conferences, bringing together innovators, practitioners, researchers, young people and families to showcase the best of youth mental health innovation from around the globe.”[22] [Emphasis added]
There’s no doubt that this conference, like his Australian award, will be used to demand more funding to increase the business stakes and drive more income into psychiatry’s pre-drugging efforts. Despite the government already allocating $103 million to McGorry, including the $25 million to further research EPPIC, he continues to call for another $800 million in funding for programs for youth mental health over the next four years.[23]
McGorry recently stated, “You have to be able to give something of yourself to people, if you are going to help them.”[24] McGorry’s brand of “helping” entails stigmatizing children with psychiatric labels that have no basis in science or medicine and then drugging them. That does not qualify as “help.” It’s betrayal. If this agenda to pre-diagnose, and pre-drug is allowed to take hold, we will truly have entered a Brave New World; Patrick McGorry’s.
[1] http://sydney.edu.au/medicine/museum/mwmuseum/index.php/McGorry,_Patrick
[2] http://www.mentalhealth.com/mag1/scz/sb-prod.html
[3] U.S. Department of Health and Human Services, “ASPE Technical Expert Panel on Earlier Intervention for Serious Mental Illness: Summary of Major Themes,” The Lewin Group, 13 May, 2009.
[4] Richard Warner, MB, DPM, is director of Colorado Recovery in Boulder, Colorado, and professor of psychiatry at the University of Colorado, “Early intervention in psychosis: Future or fad?” Centre for Addiction and Mental Health website, http://www.camh.net/Publications/Cross_Currents/Winter_2007-08/futureorfad_crcuwinter0708.html.
[5] http://www.mja.com.au/public/issues/187_07_011007/ber10341_fm.pdf
[6] http://www.mja.com.au/public/issues/187_07_011007/ber10341_fm.pdf
[7] http://www.mja.com.au/public/issues/187_07_011007/ber10341_fm.pdf
[8] http://www.mhanet.ca/documents/2008/Research-Colloquium/0920%20-%20Keynote%20MCGORRY.pdf
[9] http://www.bmj.com/cgi/content/full/337/aug04_1/a695
[10] http://bjp.rcpsych.org/cgi/content/full/187/48/s108; http://www.bmj.com/cgi/content/full/337/aug04_1/a695
[11] http://www.opednews.com/articles/Tracking-the-American-Epid-by-Evelyn-Pringle-100602-668.html
[12] http://www.behavioral.net/ME2/dirmod.asp?sid=9B6FFC446FF7486981EA3C0C3CCE4943&nm=Archives&type=Publishing&mod=Publications%3A%3AArticle&mid=64D490AC6A7D4FE1AEB453627F1A4A32&id=BFCD36BFD75E447CA63F662A633F41FB&tier=4
[13] http://www.opednews.com/articles/Tracking-the-American-Epid-by-Evelyn-Pringle-100602-668.html
[14] http://books.google.com.au/books?id=lyLfMPsnvJ0C&pg=PA136&lpg=PA136&dq=Portland+Identification+and+Early+Referral+McGorry&source=bl&ots=lEp9tdT8ZV&sig=_zlnHeFk8oqxTHSjbvLf0XQmlY4&hl=en&ei=lP0RTKThLMWPcMnSzNAH&sa=X&oi=book_result&ct=result&resnum=1&ved=0CBQQ6AEwAA#v=onepage&q&f=false
[15] http://69.5.18.33/ahrp/cms/index2.php?option=com_content&do_pdf=1&id=345
[16] http://69.5.18.33/ahrp/cms/index2.php?option=com_content&do_pdf=1&id=345
[17] http://www.iepa.org.au/ContentPage.aspx?pageID=10
[18] http://www.headspace.org.au/about/headspace-board/
[19] http://www.iepa.org.au/ContentPage.aspx?pageID=59
[20] http://www.iepa.org.au/ContentPage.aspx?pageID=59
[21] http://www.iymhconference.com.au/why-attend/
[22] http://www.iymhconference.com.au/
[23] Mental Health Update, GetUp! Action for Australia, 21 Apr. 2010, http://www.getup.org.au/blogs/view.php?id=1936&dc=1086,21560,1
[24] http://sydney.edu.au/medicine/museum/mwmuseum/index.php/McGorry,_Patrick
Related Posts
- Meet the Psychiatrist Pushing For A Brave New World of Pre-Drugging Kids—Patrick McGorry (2)
- Pharma Backed Australian of the Year Psychiatrist Wants Millions in Government Funding for Brave New World of “Pre-Drugging” Kids (18)
- Pre-Crime? Try Pre-Diagnose and Pre-Drug: Psychiatrists target infants as mental patients (8)
- Australian Psychiatrist Patrick McGorry’s push for psychiatric “early intervention” called “a prescription for disaster” (3)
- American Psychiatric Association Called Upon to Cut Drug Company Ties and Put Lives of Children Before Profits (5)
The Huffington Post— Creating Disease: Big Pharma and Disease Mongering
The Huffington Post
by Dr. Larry Dossey
June 18, 2010
You may think there is enough disease in the world already, and that no one would want to add to the diseases that we humans must deal with. But there is a powerful industry in our society that is working overtime to invent illnesses and to convince us we are suffering from them.
This effort is known as “disease mongering,” a term introduced by health-science writer Lynn Payer in her 1992 book Disease-Mongers: How Doctors, Drug Companies, and Insurers Are Making You Feel Sick. Payer defined disease mongering as “trying to convince essentially well people that they are sick, or slightly sick people that they are very ill.” This strategy has also been called “the corporate construction of disease” by Ray Moynihan, Iona Heath and David Henry in the British Medical Journal. “There’s a lot of money to be made from telling healthy people they’re sick,” they say. “Pharmaceutical companies are actively involved in sponsoring the definition of diseases and promoting them to both prescribers and consumers.”
Read entire article: http://www.huffingtonpost.com/dr-larry-dossey/big-pharma-health-care-cr_b_613311.html
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- “ADHD is a total 100% fraud. The millions of schoolchildren around the world being drugged have no disease” – Neurologist (4)
- Future Kill: Overmedicated and undermined, drug companies are capitalizing off our kids (2)
- Seriously great article: “New Psychiatry Manual Defines Almost Anyone as Insane” (0)
- Behind the Psychopharmaceutical Industrial Complex; Pharma-funded front groups masquerading as “patient advocates” (0)
- “Drugging Pre-School Children: A crime against childhood—children as young as 2 prescribed powerful anti-psychotics” (0)
Our Drug-Obsessed Nation: Obsessed with ‘feeling good’ & ‘forgetting our problems’—prescription drug abuse skyrockets
Tech Jackal
June 19, 2010
Not many people would be surprised to find that drug abuse is on the increase, but they may be surprised to find that the increase is not in illegal drug abuse but pharmaceutical drug abuse.
Emergency room visits have increased 110% over the last 5 years, due to prescription drug abuse. These visits are either for overdoses or excuses to get drugs refilled. Ten years ago, emergency room visits were for heroine abuse and other illegal drugs. Today, these visits are for Oxycodone, Hydrocodone and Hydrocodone abuse. There are also many other prescription drugs, such as antidepressants, and anti-anxiety drugs.
Today, it is a popular practice for children in high school and college to take prescription drugs to help them study and focus. Some of these prescriptions are for Addeall and Xanax. Some young people are having teeth pulled and wisdom teeth extracted just so they can get a pain prescription.
Read entire article: http://www.techjackal.net/other/2010/06/19/why-are-we-a-drug-obsessed-nation/
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- Its Not Just Celebrities Overdosing on Prescription Drugs—Its Happening Nationwide (0)
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Truly a must-read article by psychiatrist Peter Breggin: The Huffington Post— The Hazards of Psychiatric Diagnosis
The Huffington Post
By Dr. Peter Breggin
June 21, 2010
“I have a biochemical imbalance.”
“My kid is ADD.”
“I’m Bipolar.”
“I suffer from Clinical Depression.”
“I have Panic Disorder.”
Is there anything wrong with diagnosing ourselves or even accepting the mental health diagnoses of psychiatrists, family doctors, psychotherapists and other health professionals?
Psychiatric diagnoses are seductive. They seem to give us important information about ourselves and our emotional ills. They provide a key to what psychiatric drug we may need. It seems rational and scientific. In reality, psychiatric diagnosing is a kind of spiritual profiling that can destroy lives and frequently does.
First, there’s the obvious cookie cutter problem. People can’t be easily fit into the prefabricated labels contained in the Diagnostic and Statistical Manual of Mental Disorders from whence all official diagnoses emanate. Diagnoses frequently change, often in an effort to justify this or that drug. It’s not realistic, enlightening or empowering to reduce yourself or your child to one of these diagnoses. Psychiatric diagnoses are simplistic.
Consider this: Psychiatric diagnoses are always negative. There are no such diagnoses as “Exceptionally Able to Face Stress” or “Remarkably Resilient” or “Courageously Independent in the Face of Abuse.” That’s how I like to think about the people that I try to help–as heroes or potential heroes in their own life stories. I never want them to sum up, categorize or symbolize their lives in such a demeaning fashion as a psychiatric diagnosis.
But that’s only the beginning of the problem. These diagnoses imply that you or your children have a disease, especially an underlying biochemical imbalance. This can be discouraging and disempowering. Having a psychiatric diagnosis tends to make us feel helpless to transform our lives or the lives of our children for the better. It makes us feel less responsible for our own psychological and spiritual recovery and for that of our young and dependent children.
Medical diagnoses are real. When you learn you have pneumonia, diabetes or even cancer, you quickly discover that there are potential remedies. There are scientific tests and studies to diagnose the disease and to evaluate its treatment. Medical diagnoses don’t demean your mind and your soul, they describe your bodily impairments.
Psychiatric diagnoses are not genuinely medical; they are not based on biological defects or disorders. There are no objective tests. They are not about the body; they are about the mind and spirit. The medical aura that surrounds psychiatric diagnoses give them a false validity. Psychiatric diagnoses are not rooted in science but in opinion.
Psychiatric diagnoses take power and authority over your life, and the lives of your children, out of your hands. They place that power and authority in the hands of health professionals. Often it takes but a few minutes in an office to transform you or your child from a complex human being into a product on the psychiatric assembly line–and endless assembly line that can lead to a ruinous lifetime.
Perhaps worst of all, these diagnoses almost inevitably lead to the prescription of psychiatric medication to you or your child. Psychiatric drugs are toxins to the brain; they work by disabling the brain. None of them cure biochemical imbalances and all of them, every single one of them, cause severe biochemical imbalances in the brain. The adverse effects of these drugs on the brain and mind are stunning. In my recent scientific books and articles, including Medication Madness, I have demonstrated they cause medication spellbinding. Spellbound by psychoactive drugs we cannot adequately judge the impairments they create in our brain and too often we mistakenly feel “improved” when in fact our feelings have been dulled or artificially jacked up, and our judgment about ourselves and our lives have been impaired.
Read entire article: http://www.huffingtonpost.com/dr-peter-breggin/mental-health-the-hazards_b_618507.html
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- Seriously great article: “New Psychiatry Manual Defines Almost Anyone as Insane” (0)
- Psychiatry & the United States of Affliction: Are You Normal or Finally Diagnosed? (1)
- Former Head of Psychiatric Billing Bible—Theres no lab test, X-ray or any test that can prove someone has a mental disorder (0)
Huffington Post—Adderall: The Most Abused Prescription Drug in America; can cause lasting mental defects & death
The Huffington Post
By Dr. Ronald Ricker and Dr. Venus Nicolino
June 21, 2010
Adderall is abused mostly by college students and young adults. Estimates are that somewhere between 20-30 percent of college students regularly abuse Adderall.
Adderall has the dubious distinction of being the latest addition to the rogue’s gallery of lawful drugs that have made the transition to the black market. In recent years, abuse of Adderall and its imitators has increased by nearly 200 percent. Calling it an “upper” is like calling a hydrogen bomb a grenade. It is made of pure amphetamine, it’s already picked up its share of street monikers: Speed, Beans, Black Beauties, Christmas Trees, and Double Trouble, amongst others.
What are the pluses in this wonder-drug? In ordinary people it often but not always offers increased concentration. It also keeps people awake for more studying and lots more partying. It often offers a sense of euphoria and happiness and a lot better and more frequent sex, all fun at parties.
Between the glut of pop-psychology theories (often fraudulent) and the never-ending blitz of promotion by Big Pharma, people now believe they can diagnose themselves with something like ADHD as easily as ascertaining if they have a head cold and believe they have the ability to determine the correct medication for their condition. Sometimes they’re grandiosely right. Most of the time, however, they’re wrong on both counts. Even more of the time, diagnosis is irrelevant. The relevant question is where’s the “connection?” Sadly, that’s where many of us physicians fit in. We certainly don’t intend to, but often serve as the ‘connection’. Then, of course, there are those ‘patients’ and doctors that inhabit the bottom of the barrel: lying ‘patients’ and immoral doctors. Scripts can and are sold, for lots of money. Never mind the human cost, there’s money to be made and drugs to be copped. Take that prescription to the pharmacy. Or, take your money to a nearby local University. You’ll pay $30 to $40 dollars per pill for a very small amount of Adderall, usually sold to you by a student. Sales are usually student to student although the numbers of genuine drug dealers are growing rapidly in numbers, bringing with them all the problems of low-life, criminal drug dealers. Dealers recognize good business opportunities. Imagining little Johnny, having just finished Geography 1A, dealing with a real dealer chills the mind.
Illicit Adderall is taken in many ways. Most obviously, a pill can be swallowed. Pills can also be chewed, ground up and snorted, and ground up and injected (the most dangerous way of administration, by far). And then there’s ‘Stuffing’. This is accomplished by ‘stuffing’ Adderall in any orifice with a mucous membrane (anus, vagina, penis, mouth, etc.). Shooting gets the most immediate and strongest effect. Snorting is second, chewing third, and stuffing fourth. What ‘stuffing’ lacks in immediate ‘oomph’ and the loss of whatever dignity the person may retain, is made up by the length of effect and allows for the greatest amount of Adderall to be used at one time. The anus and vagina are big places and can hold a great deal of Adderall.
Sadly, there’s no free lunch.
1) Side effects are numerous. Some are minor, some serious, and some very serious. Most users have no clue as to negative side effects and usually don’t care. Ignorance, we suppose, is bliss. The most important and most negative side-effect is the Overdose. Overdose with Adderall is nasty. Results include Cardiac and/or pulmonary arrest, death, severe and lasting mental effects/defects. Which one happens to you is a matter of chance. If you’re in an Emergency Room and still alive your chances are relatively good. If you overdose at your apartment and are alone, the chance of your living is slim. If you Over Dose at a party, maybe a Frat Party, you’ve probably bought it. Drunken, high Frat boys are not known for their medical skills or even a modicum of clear thinking. Minor side effects include anxiety, and transient depression. More serious effects include heart palpitations, elevation of blood pressure, Tourette’s syndrome, seizures, stroke, and psychotic episodes or plain old psychosis.
Read entire article: http://www.huffingtonpost.com/dr-ronald-ricker-and-dr-venus-nicolino/adderall-the-most-abused_b_619549.html
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Behind the Psychopharmaceutical Industrial Complex; Pharma-funded front groups masquerading as “patient advocates”
Scoop Independent News
By Evelyn Pringle
June 22, 2010
Non-Profit Advocacy Groups
As a main component of the Psychopharmaceutical Industrial Complex, the so-called “patient advocacy” organizations have become the leading force behind the American epidemic of mental illness over the past two decades.
Drug makers, and their foundations, funnel millions of dollars to these non-profits every year. In return, the leaders recruit their members as foot soldiers to carry out the latest marketing campaigns and to provide a fire-wall so that no money trail can be tracked back to the drug companies.
Gigantic Pyramid
The psychiatric front groups form a gigantic pyramid and once pharmaceutical money enters the system through a major organization, it gets channeled into a huge spider-web that weaves through many groups, making it nearly impossible to keep track of where it came from or where it all went. Often, when the grant reports of the drug companies list a large donation to one organization, the annual reports of the other groups will show smaller gifts from that same organization.
The “charity” groups are exempt from income tax and the “contributions” funneled through them are tax deductible. The money is used for disease mongering campaigns to both market disorders and pressure public health care programs and private insurers to pay for expensive treatments.
“Presenting themselves as patient advocacy groups is highly disingenuous not only to their membership, many of which may have a sincere desire to help a loved one or a family member with mental problems, but to legislators, the press and the American public — for they have consistently lobbied for legislation that benefits the mental health and pharmaceutical industries which fund them, and not patients they claim to represent,” according to Citizens Commission on Human Rights International, a mental health watchdog group.
In a June 2, 2010, commentary titled, “Psychiatric Fads and Overdiagnosis,” on the Psychology Today website, Dr Allen Frances points out that it “is too bad that there is no advocacy group for normality that could effectively push back against all the forces aligned to expand the reach of mental disorders.”
The leaders of the supposedly “non-profits” earn outrageously high salaries, along with excellent benefit packages, while many of the patients they claim to represent are encouraged to seek federal disability payments of under $700 a month, and apply for public housing, food stamps, and Medicaid, to make ends meet. The top officials will often move from a leadership role in one organization to a higher position in another.
The drug makers rely on the front groups to do their bidding any time profits are threatened. For instance, if the FDA is considering adding a black box warning about a deadly side effect to a drug’s label, which may result in a drop in sales, representatives of front groups will show up at the FDA advisory panel hearings to testify against adding the warning.
They will also lobby FDA panels whenever there is a chance to increase profits, such as enlarging the drug customer base. In June 2009, the Psychopharmacologic Drugs Advisory Committee was set to meet to evaluate AstraZeneca’s Seroquel, Pfizer’s Geodon and Eli Lilly’s Zyprexa for use with 13 to 17 year-olds diagnosed with schizophrenia, and 10 to 17 year-olds diagnosed with pediatric bipolar disorder.
On June 8, 2009, nine front groups issued a joint statement urging the panel to vote to approve all three drugs for kids. The groups signing the letter included the American Academy of Child and Adolescent Psychiatry, American Foundation for Suicide Prevention, American Psychiatric Association, Child and Adolescent Bipolar Foundation, Children and Adults with Attention-Deficit/Hyperactivity Disorder, Families for Depression Awareness, Mental Health America, National Alliance on Mental Illness, and the National Council for Community Behavioral Healthcare.
Read entire article: http://www.scoop.co.nz/stories/HL1006/S00162.htm
Also see: http://www.cchrint.org/psycho-pharmaceutical-front-groups/
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Pre-Crime? Try Pre-Diagnose and Pre-Drug: Psychiatrists target infants as mental patients
By CCHR International
June 23, 2010
A new study, published in the American Journal of Psychiatry and headed by psychiatrist John H. Gilmore, professor of psychiatry and Director of the UNC Schizophrenia Research, claims to be able to detect “brain abnormalities associated with schizophrenia risk” in infants just a few weeks old. We would like to point out the obvious flaw in this bogus study; there is no medical/scientific test in existence that schizophrenia is a physical disease or brain abnormality to start with. There is not one chemical imbalance test, X-ray, MRI or any other test for schizophrenia, not one. So with no evidence of medical abnormality to start with, the “associated with schizophrenia risk” amounts to what George Orwell called Doublespeak (language that deliberately disguises, distorts, misleads)—it means nothing.
For decades, psychiatrists and Pharma have spouted lines to the press and public amounting to, “researchers now believe” they have medical evidence of schizophrenia as a physical/biological abnormality, or “new evidence suggests” evidence of schizophrenia as a real disease. But despite millions of dollars in research funds and countless tales of “belief” —no evidence to support the theory. One of the most common tricks employed by the Psycho/Pharmaceutical industry to mislead the public, legislators and the press, is to take X-rays or brain images of people who have been long-term users of antipsychotic drugs (known to cause brain atrophy/shrinkage) and then claim people with schizophrenia have smaller brains. They’ve spouted similar studies on kids with ADHD having smaller brains, but the bottom line to that study was that the kids with smaller brains, were…smaller kids. These are just a few of the many PR spins employed by Psycho/Pharma to try and maintain the “belief” in psychiatry, in their credibility as a science. As evidenced by the recent statement of psychiatrist Allen Frances, former DSM- IV Task Force Chairman, this belief is falling apart even within their own ranks, “There are no objective tests in psychiatry-no X-ray, laboratory, or exam finding that says definitively that someone does or does not have a mental disorder.” —Allen Frances (And Frances isn’t the only psychiatrist exposing the fraud of the biological brain disease model; click here for more.)
The logical question the press should be asking is what are the American Journal of Psychiatry and “the Director of UNC Schizophrenic Research” really after? What is their goal?
As we have exposed in the article “Australian Psychiatrist Patrick McGorry Wants His Pre-Drugging Agenda to Go Global” there is a concerted push being headed by Australian psychiatrist Patrick McGorry and other pharmaceutically funded psychiatrists for the global implementation of a new mental health paradigm; preventative mental health, i.e., pre-diagnosing (diagnosing children before they develop a “mental disorder”) and pre-drugging children ( before they show “signs” of the mental disorder). There is an obvious push for the same pre-diagnosing and pre-drugging agenda with this latest study, which claims ”major cases of schizophrenia are usually not diagnosed until a person begins witnessing its related symptoms like delusions and hallucinations as a teenager or adult . However, by that time, the disease [notice the term disease despite no medical evidence of disease] crosses the stage of preliminary treatment and is difficult to treat.” In other words, if we wait to administer drugs to them it may be too late. That along with Gilmore’s statement, “It allows us to start thinking about how we can identify kids at risk for schizophrenia very early and whether there are things that we can do very early on to lessen the risk.” This is the pre-diagnosing, pre-drugging agenda being pushed and the new “preventative” model of mental health that is more akin to a Brave New World than anything previously witnessed. And this latest “study” tells us infants are also on the agenda.
And finally, to psychiatrist and lead study author John H. Gilmore, we think you should take a lesson from the former National Institute of Mental Health (NIMH) Chief of the Center for Studies in Schizophrenia, the late Loren R. Mosher, M.D. who stated in his letter of resignation to the American Psychiatric Association, “The fact that there is no evidence confirming the brain disease attribution is, at this point, irrelevant. What we are dealing with here is fashion, politics and money. This level of intellectual/scientific dishonesty is just too egregious for me to continue to support my membership…After nearly three decades as a member it is with a mixture of pleasure and disappointment that I submit this letter of resignation from the American Psychiatric Association. The major reason for this is my belief I am actually resigning from the American Psychopharmacological Association. Luckily, the organization’s true identify requires no change in the acronym…”
To read more from Loren Mosher, including his two-year outcome study treating patients diagnosed “schizophrenic” without the use of drugs, his vehement stance against the biological psychiatric model of “disease” and more, click here.
To read the latest bogus psychiatric study, click here.
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- Meet the Psychiatrist Pushing For A Brave New World of Pre-Drugging Kids—Patrick McGorry (2)
- New York Magazine: Shrink Revolt—The controversy over psychiatric diagnoses and the DSM continues (0)
Study shows antidepressants cause major increase in miscarriages (68%) yet pregnant women still being targeted for usage
Before It’s News
June 23, 2010
This study comes on the heels of ones showing these drugs cause birth defects. But even now, regulatory agencies aren’t taking action.
Medical powers-that-be are pressing to identify women “at risk” of depression during pregnancy—likely to push them into taking anti-depressants. Now, a study has shown that SSRI and SNRI antidepressants can increase miscarriages by 68 percent. These drugs have also been associated with birth defects. Now, that is truly depressing.
A study published in the online edition of the Canadian Medical Association Journal reported a 68% increase in miscarriages in women who take modern antidepressants. Paroxetine, the SSRI sold as Paxil or Seroxat, and venlafaxine, the SNRI sold as Effexor, were especially risky, and taking more than one antidepressant was also particularly dangerous.
As previously documented in Babies of Women Taking Antidepressants Born With Deformities, Dr. Anick Bérard, PhD, one of the study’s authors, has also noted that antidepressants have been associated with birth defects. It shouldn’t, of course, come as any surprise that an agent guilty of causing birth defects would also result in miscarriages.
Overall, antidepressant use was found to increase the risk of miscarriage by 68%. Paroxetine increased the risk by 75% and venlafaxine more than doubled the risk to a 110% greater chance of spontaneous abortion.
In comparison, the increased risk of miscarriage due to untreated depression is 19 percent.
It’s obvious that increased miscarriage risks of 68 percent, 75 percent, and 110% with SSRI and SNRI treatment make a 19 percent increase in untreated pregnancy depression pale by comparison.
Read entire article: http://beforeitsnews.com/news/84/868/Antidepressants_Cause_Major_Increase_in_Miscarriages.html
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GlaxoSmithKline Enters into Confidential Settlement with 200 Families Who Say Paxil Caused Birth Defects
Fair Warning
By Lea Yu
June 25, 2010
Pharmaceutical giant GlaxoSmithKline has entered into confidential settlements with nearly 200 families who claimed that its antidepressant Paxil caused congenital birth defects.
Most of the claims alleged that babies born to mothers taking Paxil suffered heart defects. Last October, a suit filed on behalf of Lyam Kilker said he was born with three cardiac defects, including a hole between two chambers of his heart that disrupted the aorta.
Kilker’s case is the only one to have gone to trial, and a Philadelphia jury awarded Kilker’s family $2.5 million in compensatory damages. Plaintiffs argued that animal testing revealed potential problems with Paxil, but the company did not follow up with additional tests. A company memo introduced as evidence during the trial also revealed that Glaxo considered covering up any negative test results. “If neg, results can bury,” the 1997 memo said.
In 2005, the Food and Drug Administration warned doctors about a 35,000-person study that found that pregnant women on Paxil were twice as likely to have a child with defects than women taking other antidepressants.
Read entire article: http://www.fairwarning.org/2010/06/glaxosmithkline-settles-200-birth-defects-cases-linked-to-antidepressant/
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The Total Failure of Modern Psychiatry
Natural News
By David Gutierrez
June 27, 2010
Modern psychiatry went wrong when it embraced the idea that the mind should be treated with drugs, says Edward Shorter of the University of Toronto, writing in the Wall Street Journal.
Shorter studies the history of psychiatry and medicine.
Modern U.S. psychiatry has adopted a philosophy that psychological diseases arise from chemical imbalances and therefore have a very specific cluster of symptoms, he says, in spite of evidence that the difference between many so-called disorders is minimal or nonexistent. These “disorders” are then treated with expensive drugs that are no more effective than a placebo.
“Psychiatry seems to have lost its way in a forest of poorly verified diagnoses and ineffectual medications,” he writes.
Shorter calls for U.S. psychiatry to abandon its emphasis on “psychopathology” and instead adopt the European approach, which focuses on the symptoms and needs of people as individuals. Yet the draft of the latest edition of psychiatric diagnostic “Bible,” the Diagnostic and Statistical Manual of Mental Disorders (DSM), shows that U.S. psychiatry has no intention of changing course.
“With DSM-V, American psychiatry is headed in exactly the opposite direction: defining ever-widening circles of the population as mentally ill with vague and undifferentiated diagnoses and treating them with powerful drugs,” Shorter writes.
U.S. psychiatry was not always obsessed with psychopharmacology, he notes. Its early years were marked by a psychoanalytic approach that categorized mental disorders in broad, fluid categories such as “nerves,” “melancholia” or “manic-depressive illness.” These categories sufficed because similar treatments would work for people suffering from any version thereof: lithium treated both mania and severe depression, for example, while the specific symptoms experienced by an anxious person had little influence on the therapies needed.
“Our psychopathological lingo today offers little improvement on these sturdy terms,” Shorter said. “A patient with the same symptoms today might be told he has ‘social anxiety disorder’ or ‘seasonal affective disorder.’ … The new disorders all respond to the same drugs, so in terms of treatment, the differentiation is meaningless and of benefit mainly to pharmaceutical companies that market drugs for these niches.”
In the 1950s and ’60s, a new wave of psychiatrists sought to turn away from psychoanalysis — perceiving it as focusing excessively on “unconscious psychic conflicts” — and toward a more “scientific” model instead. As a result, the DSM-III introduced the vague new categories of “major depression” and “bipolar disorder,” even though evidence suggests that there is no substantial difference between the two conditions. At the same time, “major depression” absorbed what Shorter calls two very different conditions, “neurotic depression” and “melancholia.”
“This would be like incorporating tuberculosis and mumps into the same diagnosis, simply because they are both infectious diseases,” he writes.
DSM-V only continues the trend of extending the disordered label to more and more normal people, Shorter warns: “To flip through the latest draft of the American Psychiatric Association’s Diagnostic and Statistical Manual, in the works for seven years now, is to see the discipline’s floundering writ large.”
For example, the new disorder of “psychosis risk syndrome” associates a whole new class of people with full-blown schizophrenia, under the logic, Shorter says, that “even if you aren’t floridly psychotic with hallucinations and delusions, eccentric behavior can nonetheless awaken the suspicion that you might someday become psychotic.” The implication, of course, is that such people should be treated with antipsychotics.
Symptoms of “psychosis risk syndrome” include such vague descriptors as “disorganized speech.”
Other new “disorders” include hoarding, mixed anxiety-depression and binge eating. “Minor neurocognitive disorder” describes a reduction in cognitive function over time, such as that normally experienced by people over the age of 50, while “temper dysregulation disorder with dysphoria” refers to children who suffer from outbursts of temper.
“DSM-V accelerates the trend of making variants on the spectrum of everyday behavior into diseases,” Shorter says, “turning grief into depression, apprehension into anxiety, and boyishness into hyperactivity.”
Read entire article here: http://www.naturalnews.com/029088_psychiatry_failure.html
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Seriously great article: “New Psychiatry Manual Defines Almost Anyone as Insane”
Loewak
By Martijn Benders
June 27, 2010
What is wrong with a psychiatric industry that is financed by drug companies? Well isn’t that very obvious: they will try and try to classify more and more mental conditions as ‘diseases’ simply because their financers want them to do so. Nowadays children can’t behave like children anymore or they are ‘hyperactive’ or diagnosed as ‘ADHD’ and pumped full of drugs of which no one knows what the long term consequences of their use are.
At the same time, digg this, there was a recent research into which jobs have the highest suicide rates. Guess what? Yes, doctors and Psychiatrists rank amongst the highest, the most number of suicides take place in that job catagory.
Ask yourself this: why do these rather suicidally depressed people want to drug everyone? Because that’s basically what the new ‘Psychiatric Manual’ named ‘the Diagnostic and Statistical Manual of Mental Disorders (DSM).
“With DSM-V, American psychiatry is headed in exactly the opposite direction: defining ever-widening circles of the population as mentally ill with vague and undifferentiated diagnoses and treating them with powerful drugs,” Professor Shorter of the University of Toronto writes in the Wall Street Journal.
New diseases in the thick manual include the ‘Psychosis Risk Syndrome’ which is a particular type of ‘disease’ that can be streched to encompass half the world population. Twitch your eye? Behave a little weird? Have a stutter? Well, those might be signs of you having PSR which basically means you have the potential to become psychotic and, according to the manual, must be treated with drugs.
Symptoms of “psychosis risk syndrome” include vague descriptors as “disorganized speech.”
“Minor neurocognitive disorder” describes a reduction in cognitive function over time, such as that normally experienced by people over the age of 50, while “temper dysregulation disorder with dysphoria” refers to children who suffer from outbursts of temper.
The psychiatric industry has become a drugdealer culture. All these drugs do not just effect the people that take them but dissapear and mix with the environment. So ALL OF US are effected by these billions of tuns of chemical drugs that are pumped into the various water systems.
Read entire article: http://www.loewak.nl/2010/06/27/new-psychiatry-manual-defines-almost-anyone-as-insane/
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University of Copenhagen; Psychiatric Drugs Cause Birth Defects—responsibility must be taken to warn pregnant women
HealthJockey.com
June 28, 2010
Some psychotropic drugs may be recommended to treat depression as they are believed to affect the mind, emotions, and behavior of an individual. But these medications appear to elevate the risk for various birth defects. As a recent study initiated by the University of Copenhagen suggests, the consumption of psychotropic medication ought to be avoided during pregnancy.
Investigators observed the link of psychotropic medications with birth defects. They analyzed the data between 1998 and 2007 regarding Danish children under the age of 17. The study claims that the data highlighted 429 adverse drug reactions in these children. After thorough examinations the authors concluded that more than half of these cases indicated extreme birth defects including birth deformities and severe withdrawal syndromes.
Associate Professor Lisa Aagaard affirmed, “A range of serious side effects such as birth deformities, low birth weight, premature birth, and development of neonatal withdrawal syndrome were reported in children under two years of age, most likely because of the mother’s intake of psychotropic medication during pregnancy.”
In addition, the investigators inspected 4,500 pediatric adverse drug reaction reports and revealed a clear link between psychotropic medications and birth defects. It was ascertained that psychostimulants like Ritalin known to treat attention deficit disorder (ADD) was accountable in 42 percent of unfavorable reactions. And while antidepressants such as Prozac probably caused 31 percent reactions, 21 percent were contributed by antipsychotics similar to Haldol.
Read entire article: http://www.healthjockey.com/2010/06/28/birth-defects-appear-due-to-intake-of-psychotropic-medications-during-pregnancy/
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Ready for Psychiatry’s latest mental illness? Try this: Healthy Eating Disorder
Natural News
By Mike Adams
June 29, 2010
In its never-ending attempt to fabricate “mental disorders” out of every human activity, the psychiatric industry is now pushing the most ridiculous disease they’ve invented yet: Healthy eating disorder.
This is no joke: If you focus on eating healthy foods, you’re “mentally diseased” and probably need some sort of chemical treatment involving powerful psychotropic drugs. The Guardian newspaper reports, “Fixation with healthy eating can be sign of serious psychological disorder” and goes on to claim this “disease” is called orthorexia nervosa — which is basically just Latin for “nervous about correct eating.”
But they can’t just called it “nervous healthy eating disorder” because that doesn’t sound like they know what they’re talking about. So they translate it into Latin where it sounds smart (even though it isn’t). That’s where most disease names come from: Doctors just describe the symptoms they see with a name like osteoporosis (which means “bones with holes in them”).
Getting back to this fabricated “orthorexia” disease, the Guardian goes on to report, “Orthorexics commonly have rigid rules around eating. Refusing to touch sugar, salt, caffeine, alcohol, wheat, gluten, yeast, soya, corn and dairy foods is just the start of their diet restrictions. Any foods that have come into contact with pesticides, herbicides or contain artificial additives are also out.”
Wait a second. So attempting to avoid chemicals, dairy, soy and sugar now makes you a mental health patient? Yep. According to these experts. If you actually take special care to avoid pesticides, herbicides and genetically modified ingredients like soy and sugar, there’s something wrong with you.
But did you notice that eating junk food is assumed to be “normal?” If you eat processed junk foods laced with synthetic chemicals, that’s okay with them. The mental patients are the ones who choose organic, natural foods, apparently.
Read entire article: http://www.naturalnews.com/029098_orthorexia_mental_disorder.html
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Pre-Crime? Try Pre-Diagnose and Pre-Drug: Psychiatrists target infants as mental patients
By CCHR International
June 23, 2010
A new study, published in the American Journal of Psychiatry and headed by psychiatrist John H. Gilmore, professor of psychiatry and Director of the UNC Schizophrenia Research, claims to be able to detect “brain abnormalities associated with schizophrenia risk” in infants just a few weeks old. We would like to point out the obvious flaw in this bogus study; there is no medical/scientific test in existence that schizophrenia is a physical disease or brain abnormality to start with. There is not one chemical imbalance test, X-ray, MRI or any other test for schizophrenia, not one. So with no evidence of medical abnormality to start with, the “associated with schizophrenia risk” amounts to what George Orwell called Doublespeak (language that deliberately disguises, distorts, misleads)—it means nothing.
For decades, psychiatrists and Pharma have spouted lines to the press and public amounting to, “researchers now believe” they have medical evidence of schizophrenia as a physical/biological abnormality, or “new evidence suggests” evidence of schizophrenia as a real disease. But despite millions of dollars in research funds and countless tales of “belief” —no evidence to support the theory. One of the most common tricks employed by the Psycho/Pharmaceutical industry to mislead the public, legislators and the press, is to take X-rays or brain images of people who have been long-term users of antipsychotic drugs (known to cause brain atrophy/shrinkage) and then claim people with schizophrenia have smaller brains. They’ve spouted similar studies on kids with ADHD having smaller brains, but the bottom line to that study was that the kids with smaller brains, were…smaller kids. These are just a few of the many PR spins employed by Psycho/Pharma to try and maintain the “belief” in psychiatry, in their credibility as a science. As evidenced by the recent statement of psychiatrist Allen Frances, former DSM- IV Task Force Chairman, this belief is falling apart even within their own ranks, “There are no objective tests in psychiatry-no X-ray, laboratory, or exam finding that says definitively that someone does or does not have a mental disorder.” —Allen Frances (And Frances isn’t the only psychiatrist exposing the fraud of the biological brain disease model; click here for more.)
The logical question the press should be asking is what are the American Journal of Psychiatry and “the Director of UNC Schizophrenic Research” really after? What is their goal?
As we have exposed in the article “Australian Psychiatrist Patrick McGorry Wants His Pre-Drugging Agenda to Go Global” there is a concerted push being headed by Australian psychiatrist Patrick McGorry and other pharmaceutically funded psychiatrists for the global implementation of a new mental health paradigm; preventative mental health, i.e., pre-diagnosing (diagnosing children before they develop a “mental disorder”) and pre-drugging children ( before they show “signs” of the mental disorder). There is an obvious push for the same pre-diagnosing and pre-drugging agenda with this latest study, which claims ”major cases of schizophrenia are usually not diagnosed until a person begins witnessing its related symptoms like delusions and hallucinations as a teenager or adult . However, by that time, the disease [notice the term disease despite no medical evidence of disease] crosses the stage of preliminary treatment and is difficult to treat.” In other words, if we wait to administer drugs to them it may be too late. That along with Gilmore’s statement, “It allows us to start thinking about how we can identify kids at risk for schizophrenia very early and whether there are things that we can do very early on to lessen the risk.” This is the pre-diagnosing, pre-drugging agenda being pushed and the new “preventative” model of mental health that is more akin to a Brave New World than anything previously witnessed. And this latest “study” tells us infants are also on the agenda.
And finally, to psychiatrist and lead study author John H. Gilmore, we think you should take a lesson from the former National Institute of Mental Health (NIMH) Chief of the Center for Studies in Schizophrenia, the late Loren R. Mosher, M.D. who stated in his letter of resignation to the American Psychiatric Association, “The fact that there is no evidence confirming the brain disease attribution is, at this point, irrelevant. What we are dealing with here is fashion, politics and money. This level of intellectual/scientific dishonesty is just too egregious for me to continue to support my membership…After nearly three decades as a member it is with a mixture of pleasure and disappointment that I submit this letter of resignation from the American Psychiatric Association. The major reason for this is my belief I am actually resigning from the American Psychopharmacological Association. Luckily, the organization’s true identify requires no change in the acronym…”
To read more from Loren Mosher, including his two-year outcome study treating patients diagnosed “schizophrenic” without the use of drugs, his vehement stance against the biological psychiatric model of “disease” and more, click here.
To read the latest bogus psychiatric study, click here.
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- Australian Psychiatrist Patrick McGorry Wants His Pre-Drugging Agenda to Go Global (7)
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- Psychiatric Times – Let’s Call the Whole Thing Off (0)
- Meet the Psychiatrist Pushing For A Brave New World of Pre-Drugging Kids—Patrick McGorry (2)
Public reports reveal psychiatric drugs linked to 64% of all suicides in Sweden
The One Click Group
By Janne Larsson
June 29, 2010
The purpose of this investigation has been to find data about the preceding psychopharmacological treatment for all persons who committed suicide in Sweden 2007.
The conclusion is that a large percentage of the persons who committed suicide in Sweden in 2007 had received extensive treatment with psychiatric drugs within a year of and close to the suicide.
This is a report about suicides committed in Sweden (with around 9 million citizens) in 2007 and the psychiatric drug treatment that preceded these suicides.
The report has three main parts:
• It gives unique data about all suicides committed in 2007 and the psychiatric drugs that the persons received within a year of the suicide.
• It compares these data with autopsy reports about psychiatric drugs found in the blood (of 98%) of all the persons who committed suicide in 2007.
• It gives extensive information about the psychiatric drug treatment given within a year to the subgroup of persons who committed suicide in 2007 and then were reported to the National Board of Health and Welfare by reason of law 3 – one third of all suicides committed that year.
The data presented on these pages should have been published by the responsible national authorities.
A large percentage of the persons who committed suicide in Sweden in 2007 had received extensive treatment with psychiatric drugs within a year of their suicide.
The idea that persons who are depressed are suffering from “chemical imbalances”nand are deficient in the substance serotonin has been marketed by the pharmaceutical companies selling antidepressants (in the class SSRI, such as Prozac, Paxil/Seroxat, Zoloft) for more than a decade. The intensive marketing has led persons to believe that their low mood is a deficiency disease – and that it is vital to supply the substance that corrects this deficiency – the antidepressant drug.
But there is no scientific evidence that a low mood is caused by a ”chemical imbalance” in the brain 10 11. The hypothesis has been rejected with the following words by one of the most well known names in the field: “The serotonin theory of depression is comparable to the masturbatory theory of insanity.” 12 (The old theory that masturbation caused insanity.)
The Swedish medical agencies and their psychiatric consultants have used old data from forensic toxicological screenings to mislead the public and to heavily increase the use of antidepressants and other psychiatric drugs.
The most important information in this area is the patients’ medical history, the treatment history. Antidepressants, neuroleptics and other psychiatric drugs may cause harmful changes in the brain and these brain dysfunctions do not vanish when the drugs are discontinued – in many cases they cause chronic dysfunction to the brain, exemplified by the known neurological harm caused by neuroleptics. Many patients also get serious withdrawal reactions; reactions that can be so severe that they can lead to suicide.
Better sources of information are the unpublished clinical trials of psychiatric drugs done by pharmaceutical companies, and the important studies done by independent researchers. A number of these studies show that antidepressants and neuroleptics increase the risk of suicidal behaviour and directly cause effects that lead to suicide.
Read entire article: http://www.theoneclickgroup.co.uk/news.php?start=3660&end=3680&view=yes&id=4926#newspost
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Jury recommends major reforms in drug prescribing after investigation of 18-year-old’s suicide under the influence of Paxil
Pharmalot
By Ed Silverman
June 30, 2010
There have been numerous claims that a medication caused a suicide, but few lead to sweeping changes. In Canada, however, the suicide of 18-year-old Sarah Carlin, who had taken the Paxil antidepressant, is a clear exception. Following a coroner’s inquest, Canada’s provincial and federal governments were told to ensure patients are better informed about drug risks, tighten regulations on drugmakers and establish an independent agency to regulate medications.
“If these things had been in place at the time Sara was prescribed Paxil, she would be alive today,” her father, Neil Carlin, said outside court. “We consider this a great victory…We are truly confident that if these are acted upon there will be young lives saved down the road.”
For more than a year before her death, Sara had been taking Paxil, an anti-depressant, which Health Canada warns can increase the risk of suicidal events in children and adolescents under 18. The teenager hanged herself in her parents’ basement in May 2007. The inquest made numerous recommendations, which you can see if you keep reading…
Of the various recommendations, the one that is garnering the most discussion appears to be the creation of a Drug Safety Board to investigate the side effects and issue warnings to the public, doctors and hospitals. The inquest specifically recommended the new board not receive any funding from drugmakers. Drugmakers must also report all adverse events to Health Canada within 30 days.
A Glaxo spokeswoman writes to says the drugmaker “is supportive of appropriate recommendations designed to prevent similar tragedies from occurring in the future, and will give the recommendations addressed to the broader pharmaceutical industry our full attention and consideration. Sara Carlin’s death was a tragedy and we continue to express our deepest sympathies to her family.”
1. The Ministry of Health and Long-Term Care (MOHLTC) should develop a Drug Information System. This system would promote:
• Patient safety in the prescribing and dispensing of drugs.
• Collection and compilation of data in a single repository for all drugs dispensed for all Ontarians.
• Research into drug and patient safety.
2. The Drug Information System should track and monitor all drugs dispensed in Ontario regardless of who is paying for the prescription.
3. The Drug Information System should collect, compile and release data upon request to scientists such as those studying population-based health outcomes at the Institute for Clinical Evaluative Sciences.
4. The Ministry of Health and Long-Term Care should commit to developing a province-wide suicide prevention strategy as has occurred in other provinces such as Alberta.
5. The objectives of the province-wide suicide prevention strategy should include:
• Enhanced mental health and well being for Ontarians.
• The education of the public to de-stigmatize mental health disorders, including depression and substance abuse disorders.
• Improving intervention and support for Ontarians affected by depression and substance abuse.
• Improving intervention and treatment for those at risk of suicide.
• Increased efforts to reduce access to lethal means of suicide.
• Increased research activities in Ontario on suicide, suicidal behaviour and suicide prevention.
• Improved suicide and suicidal behaviour-related surveillance systems.
• Inform and educate the media into strategies when reporting deaths due to suicide to prevent ‘copy cat’ suicides from occurring.
6. Strategies in the province-wide suicide prevention strategy should be humane, effective and evidence based, respectful of community and culture-based knowledge, inclusive of research, surveillance, evaluation and reporting and reflective of evolving knowledge and practices.
7. The ministry of Health and Long-Term Care of Ontario and Government of Ontario should commit to supporting the development of a national suicide prevention strategy for all Canadians.
Read entire article: http://www.pharmalot.com/2010/06/sara-carlin-paxil-and-drug-safety-in-canada/
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The FAA better rethink allowing pilots to take antidepressants; New report says pilot in 2008 plane crash was on Zoloft
News 14 Carolina
June 30, 2010
The National Transportation Safety Board issued a report on the probably cause of a 2008 plane crash in Mount Airy that killed everyone on board. The plane stalled and crashed while circling after an aborted landing.
The NTSB says the pilot failed to maintain control of the plane during instrument flying conditions and deliberately went below the minimum descent altitude.
Officials say the pilot “displayed non-professional behavior” and that a cockpit voice recording showed that he began singing, “Save my life, I’m going down for the last time” after being cleared for approach.
Toxicology tests revealed that the pilot had the drug Zoloft in his system, and medical records revealed he had been treated for anxiety and depression. The report also said it’s not clear whether the medical conditions could account for the behavior or whether they contributed to the accident.
Read entire article: http://charlotte.news14.com/content/local_news/triad/627644/ntsb-releases-report-on-2008-mount-airy-plane-crash
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Pre-Crime? Try Pre-Diagnose and Pre-Drug: Psychiatrists target infants as mental patients
By CCHR International
June 23, 2010
A new study, published in the American Journal of Psychiatry and headed by psychiatrist John H. Gilmore, professor of psychiatry and Director of the UNC Schizophrenia Research, claims to be able to detect “brain abnormalities associated with schizophrenia risk” in infants just a few weeks old. We would like to point out the obvious flaw in this bogus study; there is no medical/scientific test in existence that schizophrenia is a physical disease or brain abnormality to start with. There is not one chemical imbalance test, X-ray, MRI or any other test for schizophrenia, not one. So with no evidence of medical abnormality to start with, the “associated with schizophrenia risk” amounts to what George Orwell called Doublespeak (language that deliberately disguises, distorts, misleads)—it means nothing.
For decades, psychiatrists and Pharma have spouted lines to the press and public amounting to, “researchers now believe” they have medical evidence of schizophrenia as a physical/biological abnormality, or “new evidence suggests” evidence of schizophrenia as a real disease. But despite millions of dollars in research funds and countless tales of “belief” —no evidence to support the theory. One of the most common tricks employed by the Psycho/Pharmaceutical industry to mislead the public, legislators and the press, is to take X-rays or brain images of people who have been long-term users of antipsychotic drugs (known to cause brain atrophy/shrinkage) and then claim people with schizophrenia have smaller brains. They’ve spouted similar studies on kids with ADHD having smaller brains, but the bottom line to that study was that the kids with smaller brains, were…smaller kids. These are just a few of the many PR spins employed by Psycho/Pharma to try and maintain the “belief” in psychiatry, in their credibility as a science. As evidenced by the recent statement of psychiatrist Allen Frances, former DSM- IV Task Force Chairman, this belief is falling apart even within their own ranks, “There are no objective tests in psychiatry-no X-ray, laboratory, or exam finding that says definitively that someone does or does not have a mental disorder.” —Allen Frances (And Frances isn’t the only psychiatrist exposing the fraud of the biological brain disease model; click here for more.)
The logical question the press should be asking is what are the American Journal of Psychiatry and “the Director of UNC Schizophrenic Research” really after? What is their goal?
As we have exposed in the article “Australian Psychiatrist Patrick McGorry Wants His Pre-Drugging Agenda to Go Global” there is a concerted push being headed by Australian psychiatrist Patrick McGorry and other pharmaceutically funded psychiatrists for the global implementation of a new mental health paradigm; preventative mental health, i.e., pre-diagnosing (diagnosing children before they develop a “mental disorder”) and pre-drugging children ( before they show “signs” of the mental disorder). There is an obvious push for the same pre-diagnosing and pre-drugging agenda with this latest study, which claims ”major cases of schizophrenia are usually not diagnosed until a person begins witnessing its related symptoms like delusions and hallucinations as a teenager or adult . However, by that time, the disease [notice the term disease despite no medical evidence of disease] crosses the stage of preliminary treatment and is difficult to treat.” In other words, if we wait to administer drugs to them it may be too late. That along with Gilmore’s statement, “It allows us to start thinking about how we can identify kids at risk for schizophrenia very early and whether there are things that we can do very early on to lessen the risk.” This is the pre-diagnosing, pre-drugging agenda being pushed and the new “preventative” model of mental health that is more akin to a Brave New World than anything previously witnessed. And this latest “study” tells us infants are also on the agenda.
And finally, to psychiatrist and lead study author John H. Gilmore, we think you should take a lesson from the former National Institute of Mental Health (NIMH) Chief of the Center for Studies in Schizophrenia, the late Loren R. Mosher, M.D. who stated in his letter of resignation to the American Psychiatric Association, “The fact that there is no evidence confirming the brain disease attribution is, at this point, irrelevant. What we are dealing with here is fashion, politics and money. This level of intellectual/scientific dishonesty is just too egregious for me to continue to support my membership…After nearly three decades as a member it is with a mixture of pleasure and disappointment that I submit this letter of resignation from the American Psychiatric Association. The major reason for this is my belief I am actually resigning from the American Psychopharmacological Association. Luckily, the organization’s true identify requires no change in the acronym…”
To read more from Loren Mosher, including his two-year outcome study treating patients diagnosed “schizophrenic” without the use of drugs, his vehement stance against the biological psychiatric model of “disease” and more, click here.
To read the latest bogus psychiatric study, click here.
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Study shows antidepressants cause major increase in miscarriages (68%) yet pregnant women still being targeted for usage
Before It’s News
June 23, 2010
This study comes on the heels of ones showing these drugs cause birth defects. But even now, regulatory agencies aren’t taking action.
Medical powers-that-be are pressing to identify women “at risk” of depression during pregnancy—likely to push them into taking anti-depressants. Now, a study has shown that SSRI and SNRI antidepressants can increase miscarriages by 68 percent. These drugs have also been associated with birth defects. Now, that is truly depressing.
A study published in the online edition of the Canadian Medical Association Journal reported a 68% increase in miscarriages in women who take modern antidepressants. Paroxetine, the SSRI sold as Paxil or Seroxat, and venlafaxine, the SNRI sold as Effexor, were especially risky, and taking more than one antidepressant was also particularly dangerous.
As previously documented in Babies of Women Taking Antidepressants Born With Deformities, Dr. Anick Bérard, PhD, one of the study’s authors, has also noted that antidepressants have been associated with birth defects. It shouldn’t, of course, come as any surprise that an agent guilty of causing birth defects would also result in miscarriages.
Overall, antidepressant use was found to increase the risk of miscarriage by 68%. Paroxetine increased the risk by 75% and venlafaxine more than doubled the risk to a 110% greater chance of spontaneous abortion.
In comparison, the increased risk of miscarriage due to untreated depression is 19 percent.
It’s obvious that increased miscarriage risks of 68 percent, 75 percent, and 110% with SSRI and SNRI treatment make a 19 percent increase in untreated pregnancy depression pale by comparison.
Read entire article: http://beforeitsnews.com/news/84/868/Antidepressants_Cause_Major_Increase_in_Miscarriages.html
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GlaxoSmithKline Enters into Confidential Settlement with 200 Families Who Say Paxil Caused Birth Defects
Fair Warning
By Lea Yu
June 25, 2010
Pharmaceutical giant GlaxoSmithKline has entered into confidential settlements with nearly 200 families who claimed that its antidepressant Paxil caused congenital birth defects.
Most of the claims alleged that babies born to mothers taking Paxil suffered heart defects. Last October, a suit filed on behalf of Lyam Kilker said he was born with three cardiac defects, including a hole between two chambers of his heart that disrupted the aorta.
Kilker’s case is the only one to have gone to trial, and a Philadelphia jury awarded Kilker’s family $2.5 million in compensatory damages. Plaintiffs argued that animal testing revealed potential problems with Paxil, but the company did not follow up with additional tests. A company memo introduced as evidence during the trial also revealed that Glaxo considered covering up any negative test results. “If neg, results can bury,” the 1997 memo said.
In 2005, the Food and Drug Administration warned doctors about a 35,000-person study that found that pregnant women on Paxil were twice as likely to have a child with defects than women taking other antidepressants.
Read entire article: http://www.fairwarning.org/2010/06/glaxosmithkline-settles-200-birth-defects-cases-linked-to-antidepressant/
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The Total Failure of Modern Psychiatry
Natural News
By David Gutierrez
June 27, 2010
Modern psychiatry went wrong when it embraced the idea that the mind should be treated with drugs, says Edward Shorter of the University of Toronto, writing in the Wall Street Journal.
Shorter studies the history of psychiatry and medicine.
Modern U.S. psychiatry has adopted a philosophy that psychological diseases arise from chemical imbalances and therefore have a very specific cluster of symptoms, he says, in spite of evidence that the difference between many so-called disorders is minimal or nonexistent. These “disorders” are then treated with expensive drugs that are no more effective than a placebo.
“Psychiatry seems to have lost its way in a forest of poorly verified diagnoses and ineffectual medications,” he writes.
Shorter calls for U.S. psychiatry to abandon its emphasis on “psychopathology” and instead adopt the European approach, which focuses on the symptoms and needs of people as individuals. Yet the draft of the latest edition of psychiatric diagnostic “Bible,” the Diagnostic and Statistical Manual of Mental Disorders (DSM), shows that U.S. psychiatry has no intention of changing course.
“With DSM-V, American psychiatry is headed in exactly the opposite direction: defining ever-widening circles of the population as mentally ill with vague and undifferentiated diagnoses and treating them with powerful drugs,” Shorter writes.
U.S. psychiatry was not always obsessed with psychopharmacology, he notes. Its early years were marked by a psychoanalytic approach that categorized mental disorders in broad, fluid categories such as “nerves,” “melancholia” or “manic-depressive illness.” These categories sufficed because similar treatments would work for people suffering from any version thereof: lithium treated both mania and severe depression, for example, while the specific symptoms experienced by an anxious person had little influence on the therapies needed.
“Our psychopathological lingo today offers little improvement on these sturdy terms,” Shorter said. “A patient with the same symptoms today might be told he has ‘social anxiety disorder’ or ‘seasonal affective disorder.’ … The new disorders all respond to the same drugs, so in terms of treatment, the differentiation is meaningless and of benefit mainly to pharmaceutical companies that market drugs for these niches.”
In the 1950s and ’60s, a new wave of psychiatrists sought to turn away from psychoanalysis — perceiving it as focusing excessively on “unconscious psychic conflicts” — and toward a more “scientific” model instead. As a result, the DSM-III introduced the vague new categories of “major depression” and “bipolar disorder,” even though evidence suggests that there is no substantial difference between the two conditions. At the same time, “major depression” absorbed what Shorter calls two very different conditions, “neurotic depression” and “melancholia.”
“This would be like incorporating tuberculosis and mumps into the same diagnosis, simply because they are both infectious diseases,” he writes.
DSM-V only continues the trend of extending the disordered label to more and more normal people, Shorter warns: “To flip through the latest draft of the American Psychiatric Association’s Diagnostic and Statistical Manual, in the works for seven years now, is to see the discipline’s floundering writ large.”
For example, the new disorder of “psychosis risk syndrome” associates a whole new class of people with full-blown schizophrenia, under the logic, Shorter says, that “even if you aren’t floridly psychotic with hallucinations and delusions, eccentric behavior can nonetheless awaken the suspicion that you might someday become psychotic.” The implication, of course, is that such people should be treated with antipsychotics.
Symptoms of “psychosis risk syndrome” include such vague descriptors as “disorganized speech.”
Other new “disorders” include hoarding, mixed anxiety-depression and binge eating. “Minor neurocognitive disorder” describes a reduction in cognitive function over time, such as that normally experienced by people over the age of 50, while “temper dysregulation disorder with dysphoria” refers to children who suffer from outbursts of temper.
“DSM-V accelerates the trend of making variants on the spectrum of everyday behavior into diseases,” Shorter says, “turning grief into depression, apprehension into anxiety, and boyishness into hyperactivity.”
Read entire article: http://www.naturalnews.com/029088_psychiatry_failure.htmll
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Seriously great article: “New Psychiatry Manual Defines Almost Anyone as Insane”
Loewak
By Martijn Benders
June 27, 2010
What is wrong with a psychiatric industry that is financed by drug companies? Well isn’t that very obvious: they will try and try to classify more and more mental conditions as ‘diseases’ simply because their financers want them to do so. Nowadays children can’t behave like children anymore or they are ‘hyperactive’ or diagnosed as ‘ADHD’ and pumped full of drugs of which no one knows what the long term consequences of their use are.
At the same time, digg this, there was a recent research into which jobs have the highest suicide rates. Guess what? Yes, doctors and Psychiatrists rank amongst the highest, the most number of suicides take place in that job catagory.
Ask yourself this: why do these rather suicidally depressed people want to drug everyone? Because that’s basically what the new ‘Psychiatric Manual’ named ‘the Diagnostic and Statistical Manual of Mental Disorders (DSM).
“With DSM-V, American psychiatry is headed in exactly the opposite direction: defining ever-widening circles of the population as mentally ill with vague and undifferentiated diagnoses and treating them with powerful drugs,” Professor Shorter of the University of Toronto writes in the Wall Street Journal.
New diseases in the thick manual include the ‘Psychosis Risk Syndrome’ which is a particular type of ‘disease’ that can be streched to encompass half the world population. Twitch your eye? Behave a little weird? Have a stutter? Well, those might be signs of you having PSR which basically means you have the potential to become psychotic and, according to the manual, must be treated with drugs.
Symptoms of “psychosis risk syndrome” include vague descriptors as “disorganized speech.”
“Minor neurocognitive disorder” describes a reduction in cognitive function over time, such as that normally experienced by people over the age of 50, while “temper dysregulation disorder with dysphoria” refers to children who suffer from outbursts of temper.
The psychiatric industry has become a drugdealer culture. All these drugs do not just effect the people that take them but dissapear and mix with the environment. So ALL OF US are effected by these billions of tuns of chemical drugs that are pumped into the various water systems.
Read entire article: http://www.loewak.nl/2010/06/27/new-psychiatry-manual-defines-almost-anyone-as-insane/
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University of Copenhagen; Psychiatric Drugs Cause Birth Defects—responsibility must be taken to warn pregnant women
HealthJockey.com
June 28, 2010
Some psychotropic drugs may be recommended to treat depression as they are believed to affect the mind, emotions, and behavior of an individual. But these medications appear to elevate the risk for various birth defects. As a recent study initiated by the University of Copenhagen suggests, the consumption of psychotropic medication ought to be avoided during pregnancy.
Investigators observed the link of psychotropic medications with birth defects. They analyzed the data between 1998 and 2007 regarding Danish children under the age of 17. The study claims that the data highlighted 429 adverse drug reactions in these children. After thorough examinations the authors concluded that more than half of these cases indicated extreme birth defects including birth deformities and severe withdrawal syndromes.
Associate Professor Lisa Aagaard affirmed, “A range of serious side effects such as birth deformities, low birth weight, premature birth, and development of neonatal withdrawal syndrome were reported in children under two years of age, most likely because of the mother’s intake of psychotropic medication during pregnancy.”
In addition, the investigators inspected 4,500 pediatric adverse drug reaction reports and revealed a clear link between psychotropic medications and birth defects. It was ascertained that psychostimulants like Ritalin known to treat attention deficit disorder (ADD) was accountable in 42 percent of unfavorable reactions. And while antidepressants such as Prozac probably caused 31 percent reactions, 21 percent were contributed by antipsychotics similar to Haldol.
Read entire article: http://www.healthjockey.com/2010/06/28/birth-defects-appear-due-to-intake-of-psychotropic-medications-during-pregnancy/
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Ready for Psychiatry’s latest mental illness? Try this: Healthy Eating Disorder
Natural News
By Mike Adams
June 29, 2010
In its never-ending attempt to fabricate “mental disorders” out of every human activity, the psychiatric industry is now pushing the most ridiculous disease they’ve invented yet: Healthy eating disorder.
This is no joke: If you focus on eating healthy foods, you’re “mentally diseased” and probably need some sort of chemical treatment involving powerful psychotropic drugs. The Guardian newspaper reports, “Fixation with healthy eating can be sign of serious psychological disorder” and goes on to claim this “disease” is called orthorexia nervosa — which is basically just Latin for “nervous about correct eating.”
But they can’t just called it “nervous healthy eating disorder” because that doesn’t sound like they know what they’re talking about. So they translate it into Latin where it sounds smart (even though it isn’t). That’s where most disease names come from: Doctors just describe the symptoms they see with a name like osteoporosis (which means “bones with holes in them”).
Getting back to this fabricated “orthorexia” disease, the Guardian goes on to report, “Orthorexics commonly have rigid rules around eating. Refusing to touch sugar, salt, caffeine, alcohol, wheat, gluten, yeast, soya, corn and dairy foods is just the start of their diet restrictions. Any foods that have come into contact with pesticides, herbicides or contain artificial additives are also out.”
Wait a second. So attempting to avoid chemicals, dairy, soy and sugar now makes you a mental health patient? Yep. According to these experts. If you actually take special care to avoid pesticides, herbicides and genetically modified ingredients like soy and sugar, there’s something wrong with you.
But did you notice that eating junk food is assumed to be “normal?” If you eat processed junk foods laced with synthetic chemicals, that’s okay with them. The mental patients are the ones who choose organic, natural foods, apparently.
Read entire article: http://www.naturalnews.com/029098_orthorexia_mental_disorder.html
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Public reports reveal psychiatric drugs linked to 64% of all suicides in Sweden
Public reports reveal psychiatric drugs linked to 64% of all suicides in Sweden
The One Click Group
By Janne Larsson
June 29, 2010
This unique report presents data about the preceding psychiatric drug treatment for all persons who committed suicide in Sweden 2007. The conclusion is that a large percentage of the persons who committed suicide had received extensive treatment with psychiatric drugs within a year of and close to the suicide.
Public reports reveal psychiatric drugs linked to 64% of all suicides in Sweden.
This is a report about suicides committed in Sweden (with around 9 million citizens) in 2007 and the psychiatric drug treatment that preceded these suicides.
The report has three main parts:
• It gives unique data about all suicides committed in 2007 and the psychiatric drugs that the persons received within a year of the suicide.
• It compares these data with autopsy reports about psychiatric drugs found in the blood (of 98%) of all the persons who committed suicide in 2007.
• It gives extensive information about the psychiatric drug treatment given within a year to the subgroup of persons who committed suicide in 2007 and then were reported to the National Board of Health and Welfare by reason of law 3 – one third of all suicides committed that year.
The data presented on these pages should have been published by the responsible national authorities.
A large percentage of the persons who committed suicide in Sweden in 2007 had received extensive treatment with psychiatric drugs within a year of their suicide.
The idea that persons who are depressed are suffering from “chemical imbalances” and are deficient in the substance serotonin has been marketed by the pharmaceutical companies selling antidepressants (in the class of antidepressant drugs called Selective Serotonin Reuptake Inhibitors, SSRIs, such as Prozac, Paxil/Seroxat, Zoloft) for more than a decade. The intensive marketing has led persons to believe that their low mood is a deficiency disease – and that it is vital to supply the substance that corrects this deficiency – the antidepressant drug.
But there is no scientific evidence that a low mood is caused by a ”chemical imbalance” in the brain. The hypothesis has been rejected with the following words by one of the most well known names in the field, Dr. David Healy,“The serotonin theory of depression is comparable to the masturbatory theory of insanity.”
The Swedish medical agencies and their psychiatric consultants have used old data from forensic toxicological screenings to mislead the public and to heavily increase the use of antidepressants and other psychiatric drugs.
The most important information in this area is the patients’ medical history; the treatment history. Antidepressants, neuroleptics and other psychiatric drugs may cause harmful changes in the brain and these brain dysfunctions do not vanish when the drugs are discontinued – in many cases they cause chronic dysfunction to the brain, exemplified by the known neurological harm caused by neuroleptics. Many patients also get serious withdrawal reactions; reactions that can be so severe that they can lead to suicide.
Better sources of information are the unpublished clinical trials of psychiatric drugs done by pharmaceutical companies, and the important studies done by independent researchers. A number of these studies show that antidepressants and neuroleptics increase the risk of suicidal behaviour and directly cause effects that lead to suicide.
Download and read the full report here; http://www.theoneclickgroup.co.uk/documents/ME-CFS_docs/Psychiatric%20Drugs%20&%20Suicide,%20Sweden%202007.pdf
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Jury recommends major reforms in drug prescribing after investigation of 18-year-old’s suicide under the influence of Paxil
Pharmalot
By Ed Silverman
June 30, 2010
There have been numerous claims that a medication caused a suicide, but few lead to sweeping changes. In Canada, however, the suicide of 18-year-old Sarah Carlin, who had taken the Paxil antidepressant, is a clear exception. Following a coroner’s inquest, Canada’s provincial and federal governments were told to ensure patients are better informed about drug risks, tighten regulations on drugmakers and establish an independent agency to regulate medications.
“If these things had been in place at the time Sara was prescribed Paxil, she would be alive today,” her father, Neil Carlin, said outside court. “We consider this a great victory…We are truly confident that if these are acted upon there will be young lives saved down the road.”
For more than a year before her death, Sara had been taking Paxil, an anti-depressant, which Health Canada warns can increase the risk of suicidal events in children and adolescents under 18. The teenager hanged herself in her parents’ basement in May 2007. The inquest made numerous recommendations, which you can see if you keep reading…
Of the various recommendations, the one that is garnering the most discussion appears to be the creation of a Drug Safety Board to investigate the side effects and issue warnings to the public, doctors and hospitals. The inquest specifically recommended the new board not receive any funding from drugmakers. Drugmakers must also report all adverse events to Health Canada within 30 days.
A Glaxo spokeswoman writes to says the drugmaker “is supportive of appropriate recommendations designed to prevent similar tragedies from occurring in the future, and will give the recommendations addressed to the broader pharmaceutical industry our full attention and consideration. Sara Carlin’s death was a tragedy and we continue to express our deepest sympathies to her family.”
1. The Ministry of Health and Long-Term Care (MOHLTC) should develop a Drug Information System. This system would promote:
• Patient safety in the prescribing and dispensing of drugs.
• Collection and compilation of data in a single repository for all drugs dispensed for all Ontarians.
• Research into drug and patient safety.
2. The Drug Information System should track and monitor all drugs dispensed in Ontario regardless of who is paying for the prescription.
3. The Drug Information System should collect, compile and release data upon request to scientists such as those studying population-based health outcomes at the Institute for Clinical Evaluative Sciences.
4. The Ministry of Health and Long-Term Care should commit to developing a province-wide suicide prevention strategy as has occurred in other provinces such as Alberta.
5. The objectives of the province-wide suicide prevention strategy should include:
• Enhanced mental health and well being for Ontarians.
• The education of the public to de-stigmatize mental health disorders, including depression and substance abuse disorders.
• Improving intervention and support for Ontarians affected by depression and substance abuse.
• Improving intervention and treatment for those at risk of suicide.
• Increased efforts to reduce access to lethal means of suicide.
• Increased research activities in Ontario on suicide, suicidal behaviour and suicide prevention.
• Improved suicide and suicidal behaviour-related surveillance systems.
• Inform and educate the media into strategies when reporting deaths due to suicide to prevent ‘copy cat’ suicides from occurring.
6. Strategies in the province-wide suicide prevention strategy should be humane, effective and evidence based, respectful of community and culture-based knowledge, inclusive of research, surveillance, evaluation and reporting and reflective of evolving knowledge and practices.
7. The ministry of Health and Long-Term Care of Ontario and Government of Ontario should commit to supporting the development of a national suicide prevention strategy for all Canadians.
Read entire article: http://www.pharmalot.com/2010/06/sara-carlin-paxil-and-drug-safety-in-canada/
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- Psychiatric Drugs, Violence and Suicide (8)
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The FAA better rethink allowing pilots to take antidepressants; New report says pilot in 2008 plane crash was on Zoloft
Comment from CCHR Int:
A few months ago, the FAA changed its rules and now allows pilots to fly planes under the influence of antidepressants (drugs documented to cause mania, psychosis, worsening depression, hallucinations, suicidal and even homicidal ideation—see this link for international studies and warnings http://www.cchrint.org/psychdrugdangers/ ). Now a new report has just been released on the 2008 Mount Airy plane crash, and toxicology tests reveal the pilot had the antidepressant Zoloft in his system. Now pay attention to this particular line of the report, “Officials say the pilot ‘displayed non-professional behavior’ and that a cockpit voice recording showed that he began singing, [yes singing] “Save my life, I’m going down for the last time.”
And this, “The NTSB [National Transportation Safety Board] says the pilot failed to maintain control of the plane during instrument flying and deliberately went below the minimum descent altitude.” Deliberately. Now look again at the documented side effects of these drugs cited above or see for yourself in the link to the psychiatric drug database. The FAA needs to reverse its ruling.
News 14 Carolina
June 30, 2010
The National Transportation Safety Board issued a report on the probably cause of a 2008 plane crash in Mount Airy that killed everyone on board. The plane stalled and crashed while circling after an aborted landing.
The NTSB says the pilot failed to maintain control of the plane during instrument flying conditions and deliberately went below the minimum descent altitude.
Officials say the pilot “displayed non-professional behavior” and that a cockpit voice recording showed that he began singing, “Save my life, I’m going down for the last time” after being cleared for approach.
Toxicology tests revealed that the pilot had the drug Zoloft in his system, and medical records revealed he had been treated for anxiety and depression. The report also said it’s not clear whether the medical conditions could account for the behavior or whether they contributed to the accident.
Read entire article: http://charlotte.news14.com/content/local_news/triad/627644/ntsb-releases-report-on-2008-mount-airy-plane-crash
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UN Calls Electroshock Treatment of Kids at Massachusetts School “Torture”
ABC News Nightline
By Katie Hinman and Kimberly Brown
June 30, 2010
It may look like any leafy New England campus, but inside one Massachusetts school for special needs children, the method of teaching at work is anything but ordinary.
The Boston-area’s Judge Rotenberg Center educates and treats enrollees ages 3 to adult, all of whom are struggling with severe emotional, behavior, and psychiatric problems, including autism-like disorders. And for about half of the 250 students here, undesirable behavior means getting hooked up to a special machine and administered an electric shock.
The skin shock treatment, used only after both a court and the student’s parents have approved, has drawn criticism for years. But after the release of a recent study by Mental Disability Rights International, Rotenberg has come under the scrutiny of no less than the United Nations, which is calling the school’s practices “torture.”
“To be frank, I was shocked when I was reading the report,” said Manfred Nowak, the UN’s Special Rapporteur on Torture. “What I did, on the 11th of May, was to send an urgent appeal to the U.S. government asking them to investigate.”
Read entire article: http://abcnews.go.com/Nightline/shock-therapy-massachussetts-school/story?id=11047334
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Senator Grassley Investigates Big Pharma’s Treatment of Drug Company Whistleblowers Who File Complaints
Bloomberg
By David Voreacos
July 1, 2010
U.S. Senator Charles Grassley asked 16 drugmakers, including Pfizer Inc., AstraZeneca Plc and Eli Lilly & Co., to reveal how they treat whistleblowers who file complaints under the False Claims Act.
Grassley, an Iowa Republican, sent letters June 28 that posed eight questions such as how companies notify employees of the law, how they treat whistleblowers and what changes they have made in response to a 2009 law extending anti-retaliation protections. Grassley’s office provided copies of the letters.
The False Claims Act lets private citizens sue on behalf of the government and share in any recovery. Whistleblowers were paid $2.39 billion from 1987 to 2009, or 16 percent of the $15.19 billion collected in False Claims lawsuits in which the U.S. government joined the case, according to the Justice Department.
“What measures does Pfizer have in place to ensure fair treatment to those filing complaints?” Grassley wrote to Chief Executive Officer Jeffrey Kindler. “Of employees who have filed complaints, have any complained of unfair treatment and/or retaliation after the filing of the complaint?”
The False Claims Act was passed by Congress in 1863 and strengthened three times since 1986. Citizens file so-called qui tam cases that remain sealed from public view as the Justice Department investigates the claims and decides whether to join the suit. Twenty-five U.S. states have their own versions of the law.
Large Settlements
Drugmakers have reached some of the largest settlements in recent years. Pfizer agreed to pay $2.3 billion over improper drug marketing, Lilly paid more than $1.6 billion to settle claims over its marketing of the drug Zyprexa, and AstraZeneca paid $520 million over marketing of its drug Seroquel.
Read entire article: http://www.bloomberg.com/news/2010-06-30/grassley-seeks-data-from-pfizer-lilly-on-how-whistleblowers-are-treated.html
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Twitterers/Text-Messagers Beware: Psychiatrists in Australia Say Text Messaging is a Mental Disorder
TVNZ
June 30, 2010
A study into modern communication and young people has identified several new disorders linked to texting on mobile phones.
Researchers say teenagers who text their friends excessively could develop one of the new disorders, News Ltd newspapers reported.
Jennie Carroll, a Melbourne technology researcher with RMIT University, says she discovered the four disorders while studying the effects of modern communication.
She says teenagers who text too much could find themselves suffering from:
- Textaphrenia: thinking you’ve heard or felt a new text message vibration when there is no message.
- Textiety: a feeling of anxiety from not receiving or sending any text messages.
- Post-traumatic text disorder: injuries related to texting, such as walking into objects by not paying attention to your surroundings.
- Binge texting: sending massive amounts of texts to build self-esteem among peers.
Read entire article: http://tvnz.co.nz/health-news/disorder-link-teenage-texting-3619511
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Prescription Pill-Popping By Far a Leading Killer as Florida’s Drug Deaths Spike 20%
Oxycodone, the addictive prescription pain-killer also known by its Purdue Pharma brand name OxyContin, directly caused more deaths in Florida in 2009 than cocaine, heroin and morphine combined. Prescription drugs as a whole are killing far more Floridians than illegal drugs, with some 8,600 deaths last year involving at least one prescription drug, according to an annual report released today by the Florida Medical Examiners Commission.
That’s 5 percent of all deaths in Florida in 2009, when 171,300 people died in the state.
The number of people killed by prescription drugs is a significant 20 percent increase over last year’s 6,200 deaths attributed to overdoses. Much of the increase is due to a spike in oxycodone addiction. The increase in prescription-drug addiction continues a trend that began in Florida 10 years ago, when prescription drugs overtook illegal drugs as leading causes of drug-related deaths.
Alcohol is also included in the examiners’ analysis, and it leads the way of all drug-related deaths, with 4,046.
The annual report is a stark look at the effects of legalized drug addiction and over-prescription of drugs, both of which affect a far larger segment of the population than recreational or illegal narcotics.
For the first time in 2009, the commission tracked deaths by region. In Flagler County’s district, which includes St. Johns and Putnam counties, 22 deaths were attributed to oxycodone (the fourth lowest number in the state’s 23 districts), with 13 of those deaths directly attributed to the drug, and nine cited as being present among other drugs that contributed to death.
Hydrocodone claimed 16 lives in the district. Cocaine contributed to 19 deaths in the Flagler district, though only four cases were directly attributed to the drug. In 15 cases, cocaine was present in the body in conjunction with other drugs that proved lethal. Overall in Florida, cocaine-related deaths (including the majority of cases where cocaine wasn’t directly the factor but was present in the body at the time of death), have fallen from a peak of 2,179 in 2007 to 1,462 in 2009. (Again, cocaine was the direct result of death in 529 cases out of those).
Ken Kramer, a researcher with the Citizens Commission on Human Rights of Florida, says the numbers underestimate the extent of the problem, because medical examiners do not track deaths attributed to antipsychotic drugs or to antidepressants, both of which carry black-box or black-label warnings. The warnings on antidepressants, required by the Food and Drug Administration, state that the drugs increase the risk of suicidal thinking and behavior in children, adolescents and young adults up to age 24. (Antidepressants include Paxil, Prozac, Zoloft, Effexor, Lexapro and Celexa.)
Anti-psychotic drugs carry a variety of black label warnings of increased mortality in elderly patients (including a death rate almost twice as high for people taking Risperdal, for example). Those drugs, prescribed and often overprescribed in nursing homes and assisted living facilities, include Abilify, Clozaril,
Geodon, Risperdal, Seroquel and Zyprexa.
“Certainly, the actual number of prescription drug deaths is higher than the annual report states,” Kramer said. “It is unknown just how much higher because the Medical Examiners Commission does not track these classes of drugs.”
Two years ago Kramer got his concern heard by the commission following an email exchange with a commissioner in which he argued that antidepressants and anti-psychotic drugs’ contributions to mortality should be part of the annual report. He was rebuffed. One examiner vsaid he had not seen “more than the occasional death caused by these types of drugs,” according to the minutes of the Aug. 13, 2008 meeting of the commission.
Read entire article: http://flaglerlive.com/7256/florida-prescription-drugs-deaths-oxycontin-oxycodone
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INFOWARS.COM — Madhouse Medical Tyranny: When Health Becomes Sickness
INFOWARS.COM
By John Galt
July 2, 2010
Dictatorships know that the battle for complete control is ultimately won or lost in the minds of the target population. As the oppression advances, it tends to move from propaganda mind control to the direct intervention into the mind via pharmaceuticals. We are now seeing the overt global coordination of the psychiatry profession to convince every resident of planet Earth that all clear thinking, healthy living, and wholesome innocence is some kind of disorder that needs to be corrected (suppressed) with drugs to render zombie-like those whose instincts afford them the ability of discernment.
We have seen this before — the role of the medical establishment in dictatorships such as Nazi Germany is well documented. It is the pre-Endgame, if you will, before the final culling takes place. The proof that we are being led by a medical tyranny to soften us up for population reduction is of course not something to make light of. However, it is absurd, because it is a manufactured attempt to re-define the natural human condition. So, let us get up to speed on our mental disorders as a gallows humor descends.
Independent Thinking
This disorder is naturally a wide-ranging one, as each unique human being tends to have opinions. Some of the more deviant forms of individuality are questioning authority and anxious distress, which includes symptoms like the “fear that something awful may happen.” Like the fear that individuality will be declared a mental disorder by a scientific dictatorship?
Emotions
The natural highs and lows that come with being a sentient human being experiencing the joys and sorrows of life apparently need to be eradicated. Happiness tests should be given to children to be sure that they feel elated at all times, and perfectly at peace with their indoctrination. If not, be sure to take your happy pills each day.
Healthy Eating
Concern for your own well-being is apparently in direct opposition to the goals of those who wish to keep the population fat, dumb, and toxic. Mike Adams gives a run-down on the latest crazy thinking associated with eating broccoli, taking vitamins and minerals, drinking purified water, and avoiding known toxins.
Pregnancy
The act of experiencing the emotions of childbirth is definitely something that needs strong legislation. Instead of thinking about creating life, and the family bonding process, it is much healthier instead to focus on the increasing numbers of disorders surrounding the most natural of processes and how the medical establishment can keep mothers worried sick about their babies.
And Now: BEING BORN
The Psychiatric Dictatorship has begun in earnest to target infants as mental patients. The amniotic world and the newly born are now under surveillance by agents of the medical elite such as John H. Gilmore, Director of the UNC Schizophrenia Research, for signs of schizophrenia. Unfortunately, Gilmore is not an isolated mad scientist; this is a global initiative. The Citizens Commission on Human Rights International recently covered the story of “Australian of the Year,” Patrick McGorry, who would like Australia to lead the world in treating mental illness. Consulting fees and research grants are raining down on pre-detection initiatives from all of the major pharmaceutical peddlers.
Read entire article: http://www.infowars.com/madhouse-medical-tyranny-when-health-becomes-sickness/
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Medscape – Psychotropic Medications Linked to Serious Adverse Drug Reactions in Children
Medscape
By Deborah Brauser
July 2, 2010
Psychotropic medications are associated with adverse drug reactions (ADRs), many of which are serious, in children younger than 17 years, according to a new database study from Danish researchers.
Results also showed that all but one of the psychotropic-related ADRs for children between the ages of birth and 2 years were serious, including birth defects such as neonatal withdrawal syndrome, ventricular septal defects, and premature labor.
These findings were “probably due to the mothers’ intake of psychotropic medicine, primarily antidepressants and antipsychotics, during pregnancy,” write the study authors.
For the overall patient population, the largest share of reported ADRs came from psychostimulants (42%), followed by antidepressants (31%) and antipsychotics (24.5%).
“The high number of serious ADRs reported for psychotropic medicines in the pediatric population should be a concern for health care professionals and physicians,” the study authors write.
In addition, “clinicians must be aware of the risks for the unborn child if they treat pregnant women with [these drugs],” coinvestigator Ebba Hansen, MSc, professor of social pharmacy and director for the FKL-Research Center for Quality in Medicine Use at the University of Copenhagen, Denmark, told Medscape Medical News.
She noted that many of the general practitioners interviewed for this study “thought that SSRI [selective serotonin reuptake inhibitor] antidepressants are harmless. Therefore, we recommend that treatment of pregnant women with psychotropic drugs should be an issue for specialists only.”
The study is published online in BMC Research Notes.
ADR Evidence Lacking
Although regulatory authorities have issued warnings about risks associated with the use of psychotropics in pediatric patients, “little evidence has been reported about the ADRs of these medicines in practice,” write the study authors.
“Overall, we have very little information about [ADRs] in children, and especially in infants, as vulnerable groups are excluded from the clinical trials that document a medication’s efficacy and safety before licensing and marketing,” said Professor Hansen.
For this study, her team evaluated 4500 ADRs in children listed in the national Danish ADR database between 1998 and 2007.
“Spontaneous ADR reporting [is] an important contributor to knowledge about safety of medicines,” the study authors write. They note that spontaneous reports are “the main source for information about new and previous unknown ADRs.”
Serious ADRs Found
Results showed that 429 of the ADRs reported during the study period were for psychotropic medications. Of these, 241 (56%) were deemed serious.
A total of 50% of the psychotropic ADRs reported were for adolescents between the ages of 11 and 17 years (n = 214), of which 45% were serious. Almost 19% were for children between the ages of birth and 2 years (n = 80).
In addition, 39% of the overall psychotropic-related ADRs were from the “nervous and psychiatric disorders” categories. When looking at sex, 59% of the total ADRs reported were for boys.
A total of 79 of the 80 ADRs associated with psychotropics in the children younger than 2 years were serious, and 2 of these were fatal (one was associated with citalopram due to chorioamnionitis and the other with fluoxetine due to persistent fetal circulation).
Finally, 40% of all psychotropic ADRs were associated with the psychostimulants methylphenidate and atomoxetine, whereas 59% of the ADRs reported for antipsychotics were associated with ziprasidone, olanzapine, and risperidone. A total of 61% of the total ADRs reported for antidepressants were with sertraline and citalopram.
Read entire article: http://www.medscape.com/viewarticle/724547
(Free registration required for Medscape)
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Hidden Facts About Ritalin; Side Effects include brain damage, psychosis, severe dependence, paranoia
New With Views
By Jon Rappoport
July 5, 2010
In 1986, The International Journal of the Addictions published a very important literature review by Richard Scarnati. It was called “An Outline of Hazardous Side Effects of Ritalin (Methylphenidate)” [v.21(7), pp. 837-841].
Scarnati listed a large number of adverse affects of Ritalin and cited published journal articles which reported each of these symptoms.
For every one of the following Ritalin effects, there is at least one confirming source in the medical literature:
• Paranoid delusions
• Paranoid psychosis
• Hypomanic and manic symptoms, amphetamine-like psychosis
• Activation of psychotic symptoms
• Toxic psychosis
• Visual hallucinations
• Auditory hallucinations
• Can surpass LSD in producing bizarre experiences
• Effects pathological thought processes
• Extreme withdrawal
• Terrified affect
• Started screaming
• Aggressiveness
• Insomnia
• Since Ritalin is considered an amphetamine-type drug, expect amphetamine-like effects
• Psychic dependence
• High-abuse potential DEA Schedule II Drug
• Decreased REM sleep
• When used with antidepressants one may see dangerous reactions including hypertension, seizures and hypothermia
• Convulsions
• Brain damage may be seen with amphetamine abuse.
Many parents around the country have discovered that Ritalin has become a condition for their children continuing in school. There are even reports, by parents, of threats from social agencies: “If you don’t allow us to prescribe Ritalin for your ADHD child, we may decide that you are an unfit parent. We may decide to take your child away.”
This mind-boggling state of affairs is fueled by teachers, principals, and school counselors, none of whom have medical training. Yet even if they did…
The very existence of the “illnesses” for which Ritalin would be prescribed is unproven. It is merely assumed.
In commenting on Dr. Lawrence Diller’s book, Running on Ritalin, Dr. William Carey, Director of Behavioral Pediatrics, Children’s Hospital of Philadelphia, has written, “Dr. Diller has correctly described… the disturbing trend of blaming children’s social, behavioral, and academic performance problems entirely on an unproven brain deficit…”
On November 16-18, 1998, the National Institute of Mental Health held the prestigious “NIH Consensus Development Conference on Diagnosis and Treatment of Attention Deficit Hyperactivity Disorder [ADHD].” The conference was explicitly aimed at ending all debate about the diagnoses of ADD, ADHD, and about the prescription of Ritalin. It was hoped that at the highest levels of medical research and bureaucracy, a clear position would be taken: this is what ADHD is, this is where it comes from, and these are the drugs it should be treated with. That didn’t happen, amazingly. Instead, the official panel responsible for drawing conclusions from the conference threw cold water on the whole attempt to reach a comfortable consensus.
Read entire article: http://www.newswithviews.com/Rappoport/jon101.htm
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New Study—Psychiatric Drugs Cause Birth Defects— pregnant women warned about smoking/alcohol but not psychiatric drugs
Lawyers and Settlements
By LAS Newswire
July 6, 2010
Copenhagen, Denmark: A recent Danish study found a high number of Prozac birth defects among the children of women who took the drug while pregnant.
The study, conducted by the University of Copenhagen, warns that Prozac and other psychotropic drugs can cause serious birth defects and other maladies, according to United Press International.
Researchers discovered 429 instances of adverse reactions when women took the drugs while pregnant. Of those 429 cases, more than half involved serious reactions and a number of them involved birth defects.
“We are constantly reminded about the dangers of alcohol use and smoking during pregnancy, but there is no information offered to women with regards to use of psychotropic medication,” researcher Lisa Aagaard said in a statement. “There is simply not enough knowledge available in this area.”
Researchers found that 42 percent of the reactions were linked to psychostimulants like Ritalin, 31 percent to antidepressants such as Prozac and 24 to anti-psychotics like Haldol.
Read entire article: http://www.lawyersandsettlements.com/articles/14468/prozac-pphn-birth-defects-lawyer-3.html
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Exclusive: Anti-Psychotics Likely to Cause Brain Damage, New Study Says
(See also these related articles from CCHR International:)
PSYCHMINDED.CO.UK
EXCLUSIVE
July 7, 2010
by Angela Hussain
Anti-psychotic drugs are likely to cause brain damage, according to a new study.
The results challenge the widely-held view that schizophrenia itself causes brain structural changes, such as less brain grey matter, bigger ventricles and larger cerebrospinal fluid (CSF) spaces, claim researchers.
The results are published in an edition earlier this year of the Psychological Medicine journal.
Researchers reviewed magnetic resonance imaging studies which had examined brain changes in patients on anti-psychotics and those of patients not on the drugs.
More than half (14) of 26 studies showed that the brains of patients on anti-psychotics had shrunk.
Of the 21 studies of patients not on anti-psychotics, five suggested brain size decreases. But no differences were reported in three studies of non-drug (known as ‘drug-naïve’) patients who had been ill for a long time.
The results are “remarkable”, claim the study’s researchers, because they contradict research purporting to rule out anti-psychotic drug-induced effects on brain size.”
Most studies of drug-naïve patients did not report or detect differences in total brain volume, global grey matter or CSF volumes between patients and controls, including three studies of untreated patients with long-term illness,” stated the researchers, including Dr Joanne Moncrieff, of the Department of Mental Health Sciences, University College London.
Upto now few studies have investigated primarily the effects of anti-psychotic treatment on brain structure.
“Overall there seems to be enough evidence to suggest that antipsychotic drug treatment may play a role in reducing brain volume and increasing CSF or ventricular spaces,” the researchers wrote. Further research is urgently required, stated the paper, entitled A Systematic Review of the Effects of Antipsychotic Drugs on Brain Volume.
Read the rest of the article here: http://psychminded.co.uk/news/news2010/july10/Anti-psychotics-likely-to-cause-brain-damage001.html
Note from CCHR: The importance of this study cannot be stated strongly enough, given the world-wide current push from the psychiatric/pharmaceutical industries for pre-diagnosing patients, including infants and children, using faulty and misleading research to try and validate schizophrenia as a brain abnormality or disease (which has never been proven) in order to push a pre-diagnosing and pre-drugging agenda. See these articles for more information;
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Just a great article: The Huffington Post—A Psychiatric Drug Story of Tragedy and Triumph by Dr. Peter Breggin
The Huffington Post
By Dr. Peter Breggin
July 7, 2010
Today I am reproducing for my readers a letter that we recently received from a woman I will call “Janice.” My wife Ginger reads and responds to most of the many communications that come to us each day through email and the networking sites she has joined. Several times a week we will get a communication that tells us that our reform work “saved my life.” I have never talked about this before because it seems self-serving, but people need to know how lifesaving it can be when health professionals dare to be honest about the hazards of psychiatric drugs and the value of empathic therapeutic approaches.
This week we received several more such letters but one stood out with its dramatic and heartfelt detail. Janice vividly portrays how she suffered not only from the disabling effects of the drugs, but also from the stigma of psychiatric diagnosis that discouraged her and made her well meaning family insist that she remain on drugs. As it seems to be in Janice’s case, the vast majority of the adults labeled “bipolar” that I see in my practice are suffering from antidepressant-induced mania in addition to whatever original life trauma led them to be diagnosed in the first place. I document several similar stories and provide the background science in Medication Madness: The Role of Psychiatric Drugs in Cases of Violence, Suicide and Crime.
Notice how much courage and motivation Janice received from a single doctor verifying for her that her problems were due to psychological trauma and not to an alleged psychiatric disease. This should lend inspiration to health care practitioners who choose to speak honestly to their patients about the origins of their emotional problems in the story of their lives.
Janice went off psychiatric drugs cold turkey and suffered greatly as a result. I never recommend this. But unfortunately too few health care providers have any idea about the merits of withdrawing from psychiatric drugs and how to help patients go about tapering off psychiatric drugs in way to minimize the withdrawal effects.
Janice’s story moves from tragedy to triumph. I offer it to you for the inspiration that it provides and I wish to thank Janice for the trust she has shown in sharing her story with us, and in allowing us to publish it anonymously.
Read entire article: http://www.huffingtonpost.com/dr-peter-breggin/a-psychiatric-drug-story_b_634352.html
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BNET: ‘The Dog Ate AstraZeneca’s Homework! Evidence on Misleading Drug Ad Disappears From Company’s Files’
BNET
By Jim Edwards
July 7, 2010
AstraZeneca (AZN) says it has lost a crucial internal document that would explain how an ad for its antipsychotic Seroquel misleadingly claimed there was “no weight gain” with the drug and described its “favorable weight profile.” But the company admits it kept the six-year-old envelope that once allegedly contained the ad’s approval certificate, according to a ruling by the U.K.’s Prescription Medicines Code of Practice Authority.
The drug industry watchdog also alleges AZ’s Seroquel management team “pressured and manipulated” executives around them in order to make sure negative data on Seroquel was buried. The PMCPA ruled that AZ had breached its code of practice, which requires companies to operate in “a professional, ethical and transparent” manner.
If there’s a lesson here for managers, it’s this: Simply winning the legal war isn’t good enough. Consumers — and your own employees, as the Seroquel case shows — expect companies to go above and beyond. (AZ has mostly won the litigation filed against it which alleges the company failed to warn patients that Seroquel causes weight gain and diabetes. It settled with the Department of Justice for $520 million.)
Many of the allegations in the PMCPA case are familiar, but what’s new is the source: One of the complainants was an unnamed male former AZ executive, employed at the company from 1992 to 2001, who from 1995 to 2000 was responsible for the medical aspects of the U.K. launch and subsequent marketing of Seroquel.*
In terms of the ad, the BBC reported in January that AZ had published a misleading ad in the British Journal of Psychiatry in April 2004. The PMCPA asked AZ to produce all the documentation behind the ad. Here’s its characterization of AZ’s response:
… for a product that had been marketed for more than 12 years in the UK, the company did not believe that it could reasonably investigate and respond to such a broad request in relation to specific clauses of the code.
The Code requires companies keep relevant documents for three years, AZ argued, and the ad itself was at least five years old, thus, “AstraZeneca had been unable to produce the certificate approving the advertisement from its archive.” But:
The Appeal Board noted from the AstraZeneca representatives at the appeal that although the job bag for the advertisement at issue still existed, it did not contain the relevant certificate.
How unfortunate!
Read entire article: http://industry.bnet.com/pharma/10008835/the-dog-ate-astrazenecas-homework-evidence-on-misleading-drug-ad-dissappears-from-companys-files/
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- AstraZeneca Denied Antipsychotic Drug’s Link to Diabetes for Years After Admitting Link to Japanese Physicians (0)
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- Drugging Kids For Profit: Powerful & dangerous antipsychotic drugs being used on kids more and more often (0)
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New Dawn Magazine—The Brave New World of Pre-Drugging Kids:Patrick McGorry & Psychosis Risk Syndrome by Jan Eastgate
New Dawn
By Jan Eastgate
July 8, 2010
Imagine being a parent taking your 10-year-old daughter to the doctor where she gasps for air and suddenly dies in your arms. You are informed afterwards that a toxic dose of prescribed medication caused her death.
Imagine leaving your house to have lunch with friends, while your husband and 11-year-old daughter are happily cuddled together watching your daughter’s favourite TV show Animal Planet. You return home hours later, walk upstairs to her bedroom and find her hanging from the valence of her bed.
Imagine your teenage son is prescribed a medicine because a teacher said he needs it to curb his disruptive behaviour. Months later he is diagnosed with severe diabetes – a known but covered up side effect by the makers of the medicine. He dies shortly afterwards from complications.
These are not isolated incidents. They are representative of those thousands of children and adolescents who died while taking prescribed psychotropic (mind-altering) drugs in the United States. In the above cases, the drugs were prescribed to treat anxiety experienced while sitting for exams or for so-called “Attention Deficit Hyperactivity Disorder” (ADHD), the symptoms of which include fidgeting, losing your pencils, not sitting still, running about or excessively climbing, and butting into other’s conversations.
Australian Child Deaths
An estimated 1,900 Australians under the age of 19 have died while on antidepressants and antipsychotics. More than 30,700 under 18-year-olds were prescribed antidepressants in 2007-2008, including 550 aged 5 and under. Side effects include hallucinations, hostility, psychosis and suicide.
During the same period, more than 9,300 children under 18 – some as young as one – were prescribed antipsychotics, costing the government $3.4 million. Of the 477 deaths reported to the Australian Therapeutic Goods Administration (TGA) linked to antipsychotics, 15 were for ages 0 to 19, including intrauterine deaths. Experts estimate only 1 percent of Adverse Drug Reactions (ADRs) are reported to the TGA, so deaths could be as high as 1,500.
Common side effects of antipsychotics include excessive weight gain, life-threatening diabetes, and an irreversible neurological effect called Tardive Dyskinesia that manifests in uncontrollable twitching of the muscles and extremities and tongue movements. Another adverse effect, Neuroleptic malignant syndrome (NMS) can cause sudden death.1 Statistics the Citizens Commission on Human Rights obtained from the TGA in 2009 revealed 14 incidents of 10 to 19 year olds experiencing NMS were reported to it.
The psychiatric drug abuse of young Australians prompted one Western Australian MP recently to call for a national inquiry into the use of psychotropic drugs in children. To date, the federal government has yet to act.
Instead, it has potentially exacerbated the situation, handing over more than one hundred million taxpayer dollars to Patrick McGorry, Professor of Youth Mental Health at the University of Melbourne, Executive Director of ORYGEN Research Centre, and founder of the youth mental health centre chain, headspace.
Read entire article: http://www.newdawnmagazine.com/articles/the-brave-new-world-of-pre-drugging-kids-patrick-mcgorry-psychosis-risk-syndrome
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- Pharma Backed Australian of the Year Psychiatrist Wants Millions in Government Funding for Brave New World of “Pre-Drugging” Kids (18)
The Daily Mail: Fussy eaters could be classified as having an ‘Eating Disorder’ in new psychiatric manual (DSM)
The Daily Mail
By Daniel Bates
July 9, 2010
They are the nightmare guests at dinner parties. But picky eaters have no control over what they like and could be suffering from an eating disorder, according to psychologists.
US researchers are considering giving picky eaters an official classification for the first time and plan to put them in the same bracket as those who have anorexia and bulimia.
Being a picky eater does not carry the same health risks as conditions like bulimia but doctors worry that over the long term it could lead to nutritional deficiencies and cause bone and heart problems.
To reflect the concerns, members of the American Psychological Association plan to label them ‘selective eaters’ and put them in the ‘not otherwise specified’ category of eating disorders.
They will make their decision for the next edition of the respected Diagnostic and Statistical Manual of Mental Disorders.
Although considered by many to be a phase that children go though, thousands of adults are picky eaters and place strict limits on what goes into their mouths.
Research into the reasons why has been inconclusive although it is thought textures and smell could account for it.
Read entire article: http://www.dailymail.co.uk/health/article-1293356/Fussy-eaters-classed-having-eating-disorder.html?ito=feeds-newsxml
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- Truly a must-read article by psychiatrist Peter Breggin: The Huffington Post— The Hazards of Psychiatric Diagnosis (0)
Heavy Doses—Drug Company J&J Pays Docs Millions for “speaking & consulting gigs”
Portfolio.com
By Brett Chases
July 9, 2010
Speaking and consulting gigs for drug companies can be lucrative for doctors.
Birmingham, Alabama, psychiatrist James E. Parker was paid more than $21,000 in speaking fees between January and March by a Johnson & Johnson company that sells mental health drugs.
Patricia Quinn, a retired Washington, D.C., physician and expert on attention deficit hyperactivity disorder, received more than $26,00 in the same period for consulting and speaking fees paid by a J&J company that markets Concerta, a leading drug for the condition.
The payments are part of just-released disclosures by J&J, which is following Pfizer Inc. and GlaxoSmithKline Plc in making public the amounts of money it pays physicians for speaking, consulting and conducting clinical trials.
Unlike other drug companies, J&J didn’t aggregate the total payments but the Wall Street Journal tallied the sum to be around $2.85 million in payments in the first quarter. J&J has a large medical device division and it pledges to divulge doctor payments for that business by next year. In three years, drug and device companies will be required to report such payments to the government as part of the new health reform law.
The financial relationships between doctors and health products companies are being scrutinized more closely by critics, Congress and the Justice Department. Pfizer’s decision to reveal its payments wasn’t voluntary. It agreed to do so as part of a $2.3 billion fraud settlement with the government. The company was accused to pushing docs to prescribe medicines for unapproved uses.
Read entire article: http://www.portfolio.com/views/blogs/heavy-doses/2010/07/09/johnson-and-johnson-pays-doctors-millions-in-first-quarter
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- Seriously great article: “New Psychiatry Manual Defines Almost Anyone as Insane” (1)
- The Huffington Post— Creating Disease: Big Pharma and Disease Mongering (0)
- “ADHD is a total 100% fraud. The millions of schoolchildren around the world being drugged have no disease” – Neurologist (4)
- American Psychiatric Association Called Upon to Cut Drug Company Ties and Put Lives of Children Before Profits (5)
Pfizer Makes Bank from DrugsThat Can Kill You—To say Pfizers been accused of wrongdoing is like saying BP had an oil spill
AlterNet
By Martha Rosenberg
July 10, 2010
The drug company Pfizer is best known for Lipitor, a drug that brings cholesterol down and Viagra, a drug that brings other things up.
But the “world’s largest research-based pharmaceutical company” which sits between Goldman Sachs and Marathon Oil on the Fortune 500, is also closely associated with a seemingly never-ending series of scandals.
To say Pfizer’s been accused of wrongdoing is like saying BP had an oil spill. Other drug companies have a portfolio of products, Pfizer has a portfolio of scandals including, but not limited to, Chantix, Lipitor, Viagra, Geodon, Trovan, Bextra, Celebrex, Lyrica, Zoloft, Halcion and drugs for osteoarthritis, Parkinson’s disease, kidney transplants and leukemia.
During one week in June Pfizer 1) agreed to pull its 10-year-old leukemia drug Mylotarg from the market because it caused more, not less patient deaths 2) Suspended pediatric trials of Geodon two months after the FDA said children were being overdosed 3) Suspended trials of tanezumab, an osteoarthritis pain drug, because patients got worse not better, some needing joint replacements (pattern, anyone?) 4) Was investigated by the House for off-label marketing of kidney transplant drug Rapamune and targeting African-Americans 5) Saw a researcher who helped established its Bextra, Celebrex and Lyrica as effective pain meds, Scott S Reuben, MD, trotted off to prison for research fraud 6) was sued by Blue Cross Blue Shield to recoup money it overpaid for Bextra and other drugs 7) received a letter from Sen. Charles Grassley (R-Iowa) requesting its whistleblower policy and 8 ) had its appeal to end lawsuits by Nigerian families who accuse it of illegal trials of the antibiotic Trovan in which 11 children died, rejected by the Supreme Court. And how was your week?
Nor does Pfizer back down when faced with legal troubles.
Even as it was under the probation of a 5-year Corporate Integrity Agreement (CIA) with Health and Human Services for withholding $20 million in Lipitor rebates owed to Medicaid in 2002, it off-label marketed its seizure drug Neurontin and entered into another CIA in 2004.
Read entire article: http://www.alternet.org/story/147467/
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The Huffington Post—Life is Not a Mental Disorder
The Huffington Post
By Ronald Ricker
July 13, 2010
The Bible (or really any religious text) can be made to say and mean anything the author wishes.
The “Bible” of psychiatry, that fabled and hoary text, the DSM-IV-TR (Diagnostic Statistical Manual of Mental Disorders written by the American Psychiatric Association), is no different. Conceived as an instrument to identify and help heal disorders of the mind, it has morphed as to both form and function. Too often, psychiatrists wield the DSM-IV-TR like a blunt instrument, desperate in their drive to assign names to supposed “mental conditions” and thus to be able to assign numbers to these “conditions.” Discover a new widely inclusive “condition,” give it a name and number and you have a winner: One more brick in the wall of sicknesses.
DSM-IV-TR is very large book. We have lots of diagnoses, the number rapidly growing. We need lots of page room. Aside from blank pages, Chapter Heading Pages, and long lists of Contributors, etc., DSM-IV-TR is chuck full of diagnoses, with detailed descriptions and code numbers for each diagnosis. This book is 952 pages long. It weighs 4.8 pounds.
There is an odd situation in DSM-IV-TR. Really odd. In its entirety, all 952 pages, there is no “No Disorder” option. Therefore, everyone is seen by DSM-IV-TR as sick, the only question being from which sickness(es) they suffer. The annual physical checkup many of us get, usually, unless there is something wrong, ends with “everything is fine.” This, apparently, doesn’t exist in mental health.
I have always felt that I was a crummy writer, starting from college and thereafter (including medical school, internship, National Institute of Mental Health, Psychiatric Residency). However, in writing this poorly written piece, while trudging through DSM-IV-TR, I found 315.2 – “Disorder of Written Expression.” It was an AH-HA moment. I may be a crummy writer, but it’s because I have a disease. Criteria, according to DSM-IV-TR, for this disease (315.2) are 3:
- a) Writing skills below those expected given the person’s chronological age, measured intelligence and age appropriate education;
- b) The disturbance in criterion A significantly interferes with academic achievement or activities of daily living that require the composition of written texts (e.g, writing grammatically correct sentences and organized paragraphs);
- c) If a sensory deficit is present, the difficulties in writing skills are in excesses of those usually associated with it.
Read entire article: http://www.huffingtonpost.com/ronald-ricker/life-is-not-a-mental-diso_b_644606.html
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SSRIs Render Unfriendly Skies—FOIA documents reveal what FAA failed to consider in allowing pilots on antidepressants to fly
Scoop Independent News
By Evelyn Pringle
July 14, 2010
The SSRI antidepressant makers are desperate to find new customers, so they recently have been focusing on capturing groups for which the drugs were usually considered off limits. The latest marketing coup managed to open up sales to roughly 614,000 American pilots.
Under a new policy announced on April 5, 2010, pilots diagnosed with depression can seek permission from the Federal Aviation Administration to take one of four SSRIs, including Eli Lilly’s Prozac, Pfizer’s Zoloft, and Forest Laboratories’ Celexa and Lexapro.
“The FAA should reverse its ruling before it’s too late and hundreds of lives are lost when a pilot becomes impulsive, suicidal or violent–or just loses his sharpness–under the influence of antidepressant medication,” said SSRI expert, Dr Peter Breggin, in an April 19, 2010 Huffington Post commentary.
The Citizens Commission on Human Rights is also calling on the FAA to rethink allowing pilots to take SSRI in light of a new report issued last month by the National Transportation Safety Board, on a February 1, 2008 plane crash in North Carolina, by a crazy acting pilot on Zoloft, that killed all six persons on board
The report said the pilot failed to maintain control of the plane during instrument flying conditions and “deliberately descended below the minimum descent altitude.” The plane stalled and crashed while circling after an aborted landing.
“Review of the cockpit voice recorder (CVR) audio revealed that the pilot had displayed some non-professional behavior before initiating the approach,” the NTSB reported.
The CVR recorded the pilot singing: “Save my life I’m going down for the last time,” before beginning a commentary in which he told passengers: “If anybody back there believes in the good Lord, I believe now would be a good time to hit your knees.”
A review of medical records documented that “from December 4, 2006 through December 31, 2007, the pilot had filled 6 prescriptions for 30 tablets of 50 mg sertraline (Zoloft),” the report said.
The records indicated that he had been treated previously with two other antidepressant medications for “anxiety and depression” and a history of “impatience” and “compulsiveness,” the NTSB noted.
An investigation of another plane crash, resulting in two fatalities in Kingsport, Tennessee, in August 2003, found Zoloft in the blood and liver of a private flight instructor, according to an accident report by the NTSB.
In the policy statement published in the Federal Register, the FAA seems to justify the use of these drugs via the fully debunked “chemical imbalance in the brain” theory when writing: “All these medications are SSRIs, antidepressants that help restore the balance of serotonin, a naturally occurring chemical substance found in the brain.”
“Increasingly accepted and prevalently used, these four antidepressants may be used safely in appropriate cases with proper oversight and have fewer side effects than previous generations of antidepressants,” the FAA wrote, with no citation to any scientific paper to back up this assertion.
In fact, the current labels on SSRIs warn that “anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), hypomania, and mania, have been reported in adult and pediatric patients treated for major depressive disorder as well as for other indications, both psychiatric and nonpsychiatric.”
“Even when not severe, these reactions impair judgment and increase the likelihood of accidents and violence,” according to Dr Breggin.
CCHR has set up a great website with a one-of-a-kind search engine that allows the public and officials to access the database on side effects reported to the FDA on SSRIs, and every other psychiatric drug. The site also has a search engine to access all the International warnings and studies on psychiatric drugs which have been summarized so they are easy to understand, even to a lay person.
Read entire article: http://www.scoop.co.nz/stories/HL1007/S00116.htm
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Glaxo To Book $2.4 billion To Settle Legal Cases, Including Avandia, Paxil
USANewsweek
July 15, 2010
British Pharma giant GlaxoSmithKline is expected to record a legal charge of $2.4 billion for the second quarter of this fiscal year in order to settle legal cases relating to its antidepressant Paxil and controversial diabetes pill Avandia. The British company announced two days ago that the money would be used not only to cover the settlements for Avandia but also other long-standing legal cases. It is learnt that the company would use the money to settle an investigation into its former factory at Cidra in Puerto Rico as well.
The news of the hefty charge, which is around 2.5 percent of the market value of the British drug maker took the edge off an expected rally in the shares after a U.S. panel allowed the company to Avandia in stores but the panel asked Glaxo to include new warnings on heart risks. “Some people might baulk at the size of the charge but probably most will say this is putting it all behind the company, so we can now look to the continuing business and view the stock on a more rational basis,” said Deutsche Bank analyst Mark Clark.
Menwhile, Glaxo did not divulge how much it was setting aside to settle legal issues related to Avandia. The company defended its decision saying that settlement terms were confidential. Earlier, it was reported that Glaxo might have to spend a whopping $6 billion to resolve legal cases related to Avandia but the panel vote allowing the company to keep the drug in market means that the company would be able to settle the claims by paying around $1 billion.
Read entire article: http://www.usanewsweek.com/news/Glaxo-To-Book-2-4-billion-To-Settle-Legal-Cases–Including-Avandia–Paxil-1279232979/
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Prescription Drug Epidemic Spreads to Babies
St. Petersburg Times
By Richard Martin
July 16, 2010
Dr. Mary Newport sees the symptoms more and more in the babies she treats: oddly stiff limbs, severe tremors, vomiting, diarrhea, insomnia, crying that never stops.
The common denominator: Their mothers were taking prescription drugs, mostly painkillers like OxyContin and Vicodin, and antianxiety drugs like Xanax during pregnancy.
Some of the moms had no idea these medications would hurt their developing babies — after all, it’s not like it’s heroin or cocaine, many think.
“They are seriously misinformed,” said Newport, medical director of Spring Hill Regional Hospital’s neonatal intensive care unit.
The prescription drug epidemic, well documented among teens and adults, now is claiming victims before they are even born. Tampa Bay area doctors and addiction specialists are reporting a dramatic increase in the number of pregnant addicts and infants needing treatment for withdrawal from prescription drugs.
The trend is reminiscent of the “crack baby” epidemic of the 1980s, when mothers used crack cocaine during their pregnancies.
But area neonatologists say that in some ways, the current trend is worse. Some women don’t understand that prescription drugs can be dangerous during pregnancy. Others decide to stop the drugs as soon as they learn they are pregnant, causing sudden withdrawal that can lead to miscarriage.
And doctors say that treating a baby with drugs like oxycodone, methadone or Xanax in the system takes longer, and involves more medication, than treatment for heroin or cocaine.
“Babies are suffering more,” said Dr. Terri Ashmeade, medical director of Tampa General Hospital’s neonatal intensive care unit. “Withdrawal patterns seem to be worse (with prescription drugs) than what we were seeing with heroin.”
Note from CCHR Int: To see for yourself what psychiatric drug reactions for infants and babies have been reported to the U.S. FDA’s medwatch system (by doctors, pharmacists, consumers etc), go to our decrypted Medwatch reports: Under the drop down menu for DRUG NAME/DRUG CLASS, scroll all the way down to the bottom until you see CLASS OF DRUGS such as ATYPICAL ANTIPSYCHOTICS or ANTIDEPRESSANTS or STIMULANTS and select one of those. In the AGE RANGE drop down menu select 0-1 year old then click GENERATE REPORT. You can do this for each class of psychiatric drug. And consider this, by the FDA’s own admission, only 1-10% of side effects are ever reported, so the actual side effects occurring in the general population are much higher.
Click here for Decrypted Medwatch Reports http://www.cchrint.org/psychdrugdangers/medwatch_psych_drug_adverse_reactions.php
Click her to read the rest of the article: http://www.tampabay.com/news/health/article1109348.ece
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Death of 7-year old prompts Florida officials to ask FDA to forbid allowing foster kids as guinea pigs in drug trials
Pharmalot
By Ed Silverman
July 19, 2010
Last year, a 7-year-old foster boy named Gabriel Myers committed suicide in Florida and, after reams of publicity and hand-wringing over the use of psychotropic medications in such children, a state task force recommended, among other things, that children never be allowed to participate in a clinical trial designed to evaluate new psychotropic meds or whether such drugs approved for adults should be given to children.
The move was prompted, in part, because a Florida psychiatrist, Sohail Punjwani, who treated the boy before he committed suicide, received an FDA warning letter for failing “to protect the rights, safety and welfare” of children enrolled in clinical trials (back story). Before the suicide, the psychiatrist prescribed to kids several drugs, some of which weren’t approved by the FDA for use on children and had been linked to dangerous side effects, including an increased risk of suicide among children (back story).
As part of the follow-up, George Sheldon, who head’s Florida’s Department of Children and Families, wrote FDA commish Margaret Hamburg for info about any foster children who might have participated in clinical trials for psychotropic meds (read the letter) and asked the FDA to forbid foster kids from participating in these trials. Last month, the agency wrote back to say the agency does not agree with a “blanket prohibition” on enrolling foster children. Why? Such a policy fails to account for the greater risk of off-label prescribing and research involving children can yield benefits that cannot be obtained by tracking usage in adults, Jill Warner, acting associate commissioner for the FDA’s Special Medical Programs, wrote back (see here). Drugmakers, by the way, also have something at stake – they receive an extra six months of marketing exclusivity in return for having conducted the pediatric trials.
We asked Florida officials if they are rethinking their position. The answer? No way. The state is resolute.
Read entire article: http://www.pharmalot.com/2010/07/florida-tells-fda-no-children-in-psychotropic-trials/?utm_source=feedburner&utm_medium=email&utm_campaign=Feed%3A+Pharmalot+%28Pharmalot
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New study linking anti-psychotics to brain damage raises alarm bells with health campaigners & human rights groups
Black Mental Health UK
By Zephaniah Samuels
July 18, 2010
Findings from a new study that shows that anti-psychotic drugs are likely to cause brain damage has raised alarm bells among health campaigners and human rights groups.
Effects of antipsychotics on brain volume
Entitled ‘A systematic review of the effects of antipsychotic drugs on brain volume ,’ the results of this study dispel the widely-held view that schizophrenia itself causes brain structural changes. ‘Some evidence points towards the possibility that antipsychotic drugs reduce the volume of brain matter and increase ventricular or fluid volume. Antipsychotics may contribute to the genesis of some of the abnormalities usually attributed to schizophrenia,’ the report says.
Published in the journal of Psychological Medicine these new findings are based on a review of the effects of antipsychotic drugs on the brain. The findings published earlier this year, have raised alarm among race equality and human rights groups who are increasingly concerned about the over-diagnosis of ‘schizophrenia’ among people from African Caribbean people communities.
The annual Count Me In Census report logs the ethnic origin of those admitted into psychiatric care including those detained against their will under the Mental Health Act.
For the past four years census findings have shown that rates of forced detention of black people under the Act continue to rise while falling for the rest of the population. The results of the latest 2009 Census published earlier this year again confirmed health campaigners worst fears, that absolutely no improvement has been made to reduce the detention rate of black people sectioned under the Mental Health Act despite the former government’s million pound programmed to address the racism and within mental health service.
African Caribbean’s routinely given diagnosis of schizophrenia
Once in the system evidence shows that black people are routinely given a diagnosis of schizophrenia even though there is no biological evidence to show that this group have higher rates of mental ill health than their white counter parts.
The diagnosis of schizophrenia is routinely accompanied by a regime of antipsychotic medication, with little evidence of those who enter the system ever making a full recovery.
A report by the now defunct Mental Health Act Commission entitled, Risks, Rights and Recovery published in 2008 show that over stretched staff are regularly give patients high doses of medication in order to make patients more easy to manage.
This latest paper challenges the view that schizophrenia itself causes brain structural changes, such as less brain grey matter, larger ventricles and more cerebrospinal fluid (CSF) spaces, researchers say. The team responsible for this work reviewed magnetic resonance imaging studies, which had assessed brain changes in patient on anti-psychotic and those of patients not on the drugs.
Over half of the 26 studies showed that the brains of patients on anti-psychotics had shrunk. This was compared to the 21 studies of patients who had not be given anti-psychotics, where just five showed brain size decreases. However no differences were reported in three studies of non-drug patients who had been ill for a long time.
Read entire article: http://www.blackmentalhealth.org.uk/index.php?option=com_content&task=view&id=805&Itemid=117
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GlaxoSmithKline settles case with woman who linked her use of antidepressant Paxil to the death of her infant son
The Associated Press
By Wayne Ortman
July 19, 2010
SIOUX FALLS, S.D. — A settlement has been reached in a lawsuit filed against a pharmaceutical company by a Watertown woman who linked her prescribed use of Paxil to the death of her infant son, according to court files.
Jennifer Berg of Watertown sued SmithKline Beecham, doing business as GlaxoSmithKline, in October 2007. The complaint said Nathan Berg died in 2004 because of a heart disorder caused by her use of the antidepressant Paxil while she was pregnant.
The federal court lawsuit sought unspecified damages from the company for failing to warn of a link between the two. Letters from her attorneys to the presiding judge indicate there’s a settlement. No settlement documents have been filed in court.
Lawyers at a California firm handling the case for Berg did not immediately return a phone call Monday for comment.
GlaxoSmithKline said last week that it expects to take a $2.36 billion charge against second-quarter earnings for settlements, agreements to settle and other provisions for long-standing legal cases over Paxil, the diabetes drug Avandia and other issues. The company said settlement details would be confidential.
According to the lawsuit, Nathan Berg was born Aug. 20, 2004 at Watertown and was immediately transferred to a Minneapolis hospital where he died 58 days later of Persistent Pulmonary Hypertension of the Newborn (PPHN), a disorder which prevents proper oxygenation of the blood.
“At the time Paxil was prescribed to Ms. Berg, GSK (GlaxoSmithKline) knew or should have known through pre-market studies and post-market studies and reports that Paxil was associated with an increased risk of PPHN in babies whose mothers ingested Paxil during pregnancy,” according to the lawsuit.
Read entire article: http://www.google.com/hostednews/ap/article/ALeqM5j7UU4otrHhelqaJFcC3ttvwj4bYgD9H29RK00
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The Los Angeles Examiner: Psychiatric Overdiagnosis Means “Normal” Could Become Obsolete
Examiner.com
By jenny Westberg
July 13, 2010
Are you normal? Are you sure?
A growing number of behaviors and moods are being relabeled as mental disorders, according to two recent articles. Sadness, shyness, personality quirks and the ups and downs of everyday life may qualify almost anyone for a psychiatric diagnosis, effectively pathologizing normality.
Allen Francis, MD writes in the Psychiatric Times that almost everyone meets the criteria for one or another of the conditions listed in the Diagnostic and Statistical Manual of Mental Disorders, the book psychiatrists use to determine whether you have a mental illness. The fifth edition of the manual (DSM-5), due in 2013, will relax these criteria even further, giving psychiatric labels to even more people.
According to 2010 figures from the National Institute of Mental Health (NIMH), more than 25 percent of the adult population has a diagnosable mental disorder. That’s approximately 60 million people. A prospective study found that, by age 32, half of U.S. adults could be diagnosed with anxiety; 40 percent with depression; and 30 percent with alcohol abuse or dependence.
With criteria proposed for the DSM-5, psychiatrists could diagnose “Nicotine Use Disorder” or “Caffeine-Induced Sleep Disorder.” If your child has temper tantrums, that’s one of the signs of “Temper Dysregulation Disorder with Dysphoria.” Bad dreams? It could be a case of “Nightmare Disorder.”
Why is this a problem? Mental illness carries a stigma. A diagnostic label can follow you for the rest of your life. It is shared with your insurance company. Your family and friends might make certain assumptions about you. Your doctor may insist you need psychiatric drugs.
More and more behaviors, however, are being stamped as “mental illnesses.”
Francis writes that individual differences that were once accepted as normal have become medicalized. Our society, he says, has become perfectionistic and intolerant of even short-term distress.
Read entire article: http://www.examiner.com/x-31400-Portland-Mental-Health-Examiner~y2010m7d13-Psychiatric-overdiagnosis-means-normal-could-become-obsolete
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Psychiatric Meds 101: A Surprising Discovery
By Shane “The People’s Chemist” Ellison
Author, Over-The-Counter Natural Cures
I may be a perfect candidate for psychiatry.
I ask questions with period marks to shorten conversations. I avoid eye contact with strangers in fear (maybe it’s anxiety) that I might learn too much about them. I secretly think that Metallica would be making better music if they went back to bludgeoning themselves with party drugs and alcohol, instead of “therapy.” I’m trying to master the Law of Un-attraction to shield myself from a “real job,” small homes and junky cars. And, I’m constantly giving my children advice, only to give it to myself.
Psychiatry, can your drugs help me?
Perhaps these questions are what motivated me to pursue a career as a drug design chemist, winning multiple awards for my work. Nothing gets me more excited than drugs and how they affect the body (except my wife’s abs). I’ve studied their molecular anatomy, risked life and limb to mix and match explosive chemicals in a round bottom flask, and even sold my soul to Big Pharma in exchange for a lab bench and chemical hood.
During this time, I’ve made some surprising discoveries about psychiatric meds, which include antidepressants, antipsychotics, stimulants, and anti-anxiety drugs. Understanding what I’ve learned will protect you from the flood of side effects that are now being discovered at breakneck speeds, courtesy of the myriad of patients being prescribed psychiatric drugs in the name of mental health.
Your Own Personal Hell
Antidepressants strive to increase the levels of a “coping” molecule known as serotonin in the brain. It supposedly helps us find happiness when it’s covered in an avalanche of nastiness. But, it’s never been proven. Still, the drugs attempt to boost serotonin by “selectively” stopping the “reuptake” among brain cells. This is where the whole SSRI acronym came from—“selective serotonin reuptake inhibitor.” It’s a slick name, but a stupid idea. Nothing is selective in the body.
While trying to block the reuptake of serotonin, antidepressants can also prevent its release and that of another brain compound known as dopamine. The areas of the brain responsible for release and reuptake of these neurotransmitters are so damn similar (after all, they work on the same molecule) that an antidepressant drug isn’t smart enough to understand which one it is supposed to work on. So it does what any dumb drug would do, it blocks both. That’s why users usually carry a glassy stare in their eye. Fully under the psychiatric spell, they’ve tuned out.
Deep sadness, fear, anger and aggression can set in over time. By removing serotonin and dopamine from the brain, long-term antidepressant users can’t find or feel happiness. Instead, they may become buried in the avalanche of nastiness. And if you can’t find or feel happiness in life, what’s the point? What’s going to stop you from snapping your own neck or spraying bullets on your classmates? Not much when you live in your own personal antidepressant hell.
Think this is all opinion?
According to the FDA, antidepressants can cause suicidal thoughts and behavior, worsening depression, anxiety, panic attacks, insomnia, irritability, hostility, impulsivity, aggression, psychotic episodes and violence. Some even cause homicidal ideation according to the manufacturers. Many long-term antidepressant users will tell you they no longer feel normal emotions—they’re numb, like zombies.
But the side effects of these drugs aren’t limited to hijacking your feelings and emotional state, causing violent and psychotic states. Physical side effects occur too and include abnormal bleeding, birth defects, heart attack, seizures and sudden death. Over one hundred and seventy drug regulatory warnings and studies have been issued on antidepressants, to sound the alarm on these side effects.
For Elephant Use Only
Psychiatrists prescribe antipsychotic meds such as Zyprexa and Seroquel, for anything from schizophrenia, bipolar disorder, delusional disorder, psychotic depression, autism or anything else they can think of, even “pervasive developmental disorder,” which is perfect for boosting sales because it targets children who suffer from irritability, aggression, and agitation. It’s a shame ‘cause these drugs are good for nothing but sedating irate elephants, not curing psychiatric disease.
According to a study published in Psychological Medicine, antipsychotic drugs cause brains to shrink – they lessen brain matter and volume. Originally designed for those deemed “schizophrenic,” the drug companies came up with a brilliant marketing campaign to sell these drugs to a much wider market—unsatisfied antidepressant users. You’ve probably seen the ads—if your “depression medication” isn’t working, then don’t blame the drug; you may just have bipolar disorder!”
Once swallowed, antipsychotics sail through the blood stream where they’re carried to the brain. Like a giant oil spill, antipsychotics cover the brain in a medicinal slick, where brain wave transmission is blocked. Users become devoid of normal brain activity. Motivation, drive and feelings of reward are shunted. If psychiatry considers this a “treatment,” they’re the crazy ones.
If you’ve ever seen someone who has suffered from the “spill” courtesy of following doctors orders, you can’t mistake one of the most common side effects, it’s called Akathisia. Involuntary movements, tics, jerks in the face and the entire body can become permanent side effects for antipsychotic users.
Antipsychotics also cause obesity, diabetes, stroke, cardiac events, respiratory problems, delusional thinking and psychosis. Drug regulators from the U.S., Canada, United Kingdom, Ireland, Australia, New Zealand and South Africa warn that they can also lead to death. I wouldn’t be surprised if psychiatrists considered this a cure…
Use This to Jump The Grand Canyon
If you’re going to attempt to jump your scooter over the Grand Canyon, or ride your snowboard off Kilimanjaro, stimulants are great. They flood the brain with dopamine and trigger an inhuman surge of adrenaline, responsible for making you believe life is grand, despite eminent death. Outside of that, you’re either a speed freak, a college student trying to learn an entire semester of Biology 101 in 4 hours, or a fifth grader “following doctor’s orders.”
Top stimulants being prescribed today are nothing more than a mix of amphetamines packaged into trade names like Adderall, Dexedrine and Ritalin. Street thugs sell it as meth, poor man’s cocaine, crystal, ice, glass and speed. It’s no wonder kids are now abusing Ritalin, Adderall and these drugs more than street drugs, they’re cheaper to get and they’re “legal,” hence the term kiddie cocaine.
Even the U.S. Drug Enforcement Administration (DEA) categorizes Ritalin in the Schedule ll category, meaning a high potential for abuse—just like cocaine and morphine. All of them have the same effects regardless of how they’re named: Central nervous system overload leading to heart attack and/or heart failure. And kids are dropping faster than Meth Heads at Raves…
I’m not exaggerating.
Eleven international drug regulatory agencies and our own FDA has issued warnings that stimulants like Ritalin cause addiction, depression, insomnia, drug dependence, mania, psychosis, heart problems, stroke and sudden death.
Bash Your Head in with Anti-Anxiety Drugs
If you’re not man enough for a drug that could sedate an elephant like antipsychotics, then psychiatrists will prescribe anti-anxiety meds, particularly benzodiazepines. Choosing between the two is akin to deciding whether or not you should be hit in the head with an aluminum bat or a wooden one; anti-anxiety meds being the latter.
Discovered in the stinky chemistry labs of Hoffman La Roche in 1955, anti-anxiety meds aim to trigger sleep receptors in the brain, just slightly. So, rather than being riddled with anxiety, you are put to sleep, halfway. It’s “treatment,” and psychiatrists have been “practicing it for decades.” But, it has yet to work, because drugging your problems away is more dangerous than anxiety. The use of anti-anxiety meds is coupled with a host of nasty side effects such as seizures, aggression and violence once the drug wears off. Hallucinations, delusional thinking, confusion, abnormal behavior, hostility, agitation, irritability, depression and suicidal thinking are all possible outcomes according to Big Pharma’s heavily guarded research papers.
Getting off the drugs could be harder than abandoning a heroin addiction. Some have described withdrawal from “benzos” being akin to pulling hundreds of fish hooks out of their skin, without anesthesia. If you doubt their addictive nature, go to Google search and type in a few of the leading anti-anxiety drugs like Klonopin or Xanax and here is what you’ll find:
“Klonopin withdrawal” 1,860,000 results
“Xanax withdrawal” 1,980,000 results
Exposing Psychiatry: How to Get The Truth
In total, the side effects of psychiatric meds spread far and wide. And most are hidden from patients and doctors alike. Fortunately, Citizens Commission on Human Rights has solved this problem with a state-of-the-art database that allows people to search through the adverse reaction reports sent to the FDA on psychiatric drugs. It also provides international drug regulatory agency warnings and studies published on the side effects of the drugs.
So, can psychiatry help me? No. And that’s surprising because psychiatric meds are some of the biggest selling drugs, poised to seal the hopes and dreams of millions. Regardless of what mental state I might be in (or anyone else for that matter), there is not a single drug that cures, treats or solves the perceived problems of mental health.
While people can suffer miserably from emotional or mental duress that can hinder their lifestyle, the pseudo-science of psychiatry has yet to solve any of these problems, and in fact only contributes to poor health as seen by the wide array of side effects. Marketing campaigns and ghostwritten medical journals are designed to obscure these facts. But the psychiatric drug side effect database courtesy of CCHR ensures that all patients have access to the truth, to the documented facts, which could save their life or that of a loved one.
About the Author
Shane Ellison holds a masters degree in organic chemistry and is the author of Over-The-Counter Natural Cures. An award winning chemist, he has been quoted by USA Today, Shape, Woman’s World, as well as Women’s Health and appeared on Fox and NBC as a natural medicine advocate. Sample his book free at www.thepeopleschemist.com
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Psychiatric Meds 101—A layman’s guide to drug side effects—by award winning Scientist Shane Ellison
By Shane “The People’s Chemist” Ellison
Author, Over-The-Counter Natural Cures
I may be a perfect candidate for psychiatry.
I ask questions with period marks to shorten conversations. I avoid eye contact with strangers in fear (maybe it’s anxiety) that I might learn too much about them. I secretly think that Metallica would be making better music if they went back to bludgeoning themselves with party drugs and alcohol, instead of “therapy.” I’m trying to master the Law of Un-attraction to shield myself from a “real job,” small homes and junky cars. And, I’m constantly giving my children advice, only to give it to myself.
Psychiatry, can your drugs help me?
Perhaps these questions are what motivated me to pursue a career as a drug design chemist, winning multiple awards for my work. Nothing gets me more excited than drugs and how they affect the body (except my wife’s abs). I’ve studied their molecular anatomy, risked life and limb to mix and match explosive chemicals in a round bottom flask, and even sold my soul to Big Pharma in exchange for a lab bench and chemical hood.
During this time, I’ve made some surprising discoveries about psychiatric meds, which include antidepressants, antipsychotics, stimulants, and anti-anxiety drugs. Understanding what I’ve learned will protect you from the flood of side effects that are now being discovered at breakneck speeds, courtesy of the myriad of patients being prescribed psychiatric drugs in the name of mental health.
Your Own Personal Hell
Antidepressants strive to increase the levels of a “coping” molecule known as serotonin in the brain. It supposedly helps us find happiness when it’s covered in an avalanche of nastiness. But, it’s never been proven. Still, the drugs attempt to boost serotonin by “selectively” stopping the “reuptake” among brain cells. This is where the whole SSRI acronym came from—“selective serotonin reuptake inhibitor.” It’s a slick name, but a stupid idea. Nothing is selective in the body.
Read the rest of this article here: http://www.cchrint.org/2010/07/20/psychiatric-meds-101-a-surprising-discovery/
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Glaxo To Pay $1Billion To Settle Paxil Birth Defect Cases
Pharmalot
By Ed Silverman
July 21, 2010
In an effort to get its arms around massive litigation, GlaxoSmithKline has agreed to settle yet another wad of product-liability lawsuits involving one of its popular meds. The latest deal involves an agreement to pay more than $1 billion to settle some 800 cases alleging its Paxil antidepressant caused birth defects in children borne to women who took the drug, Bloomberg News writes.
The move comes after a Pennsylvania state court jury last October awarded a woman $2.5 million in damages for failing to properly warn docs and pregnant women about the risks of the antidepressant. This case, which was filed by the family of a three-year-old boy who was born with heart defects his mother blamed on the drug. It was the first of 600 such lawsuits and was seen as a test of Glaxo’s vulnerability (background).
Last week, Glaxo disclosed plans to take a $2.4 billion charge in its second quarter to settle product-liability lawsuits over its Avandia diabetes pill, litigation involving the Paxil antidepressant and a US government investigation into its manufacturing site at Cidra, Puerto Rico.
The Paxil deal, which would provide an average payout of more than $1.2 million to families of the affected children, leaves more than 100 similar cases pending. The birth-defect settlements bring to more than $2 billion the amount Glaxo has agreed to pay to resolve a variety of Paxil-related suits, including claims the pill caused suicides or attempted suicides and addiction problems, Bloomberg writes.
Read the entire article here: http://www.pharmalot.com/2010/07/glaxo-to-pay-1b-to-settle-paxil-birth-defect-cases/
See all international studies/warnings on Paxil: http://www.cchrint.org/psychdrugdangers/drug_warnings.php
See what doctors, pharmacists, health care providers and others have reported to the US FDA on Paxil side effects (such as birth defects): http://www.cchrint.org/psychdrugdangers/medwatch_psych_drug_adverse_reactions.php
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First peer reviewed study documenting psych drugs to cause violence—Chantix anti-anxiety drug sold for quitting smoking
Pharmalot
By Ed Silverman
July 22, 2010
For the past three years, the Chantix smoking cessation pill has caused a stir after being associated with suicidal behavior and vivid dreams (see here and here). Consequently, the government banned the Pfizer drug for pilots and licenses wouldn’t be issued to truck drivers taking the med (see this). The FDA subsequently imposed a risk management program and Pfizer added warnings.
Now, a new study in The Annals of Pharmacotherapy finds Chantix is not only associated with violent and agressive thoughts and acts, but has also identified some of the common characteristics among people using the pill and their subsequent behavior. The drug “does have warnings about psychiatric side effects, but it skims over aggression/violence towards others to focus mainly on suicidal behaviors,” says Thomas Moore, one of the co-authors and a senior scientist at the Institute for Safe Medication Practices, a non-profit that has issued reports previously about Chantix side effects.
“We believe this may be the first scientific report to examine the characteristics of aggression/violence as a psychiatric side effect for any prescription drug. What do these cases look like? A question answered for possibly the first time. We found the details striking and chilling. This is the first time we know of that aggression/violence has been clearly documented as a side effect in a peer reviewed scientific journal. This raises the question of whether (Chantix) is suitable for use in the military, by police and others who are already in stress situations. One key characteristic of these events is uncontrollable rage. Not a good side effect for people paid to carry guns.”
The researchers obtained 78 adverse event reports from the FDA MedWatch database containing medical terms describing possible acts or thoughts of aggression/violence; four more cases came from clinical trials, and three others came from published literature. Ultimately, they used 26 case reports for study and these described 10 events with assault, nine cases of homicidal ideation and seven instances of other thoughts or acts of aggression/violence. They noted that the patient population was predominantly middle-aged women, but “an unlikely age group and sex for assault and acts of violence toward others.”
“In all 26 cases,” they write, “the acts or thoughts of violence appeared to be inexplicable and unprovoked. A woman struck her 17-year-old daughter in the mouth while the daughter was driving a car, with a young granddaughter also present. A 42-year-old man punched a stranger at a bowling alley. The stranger and two friends responded and knocked out the subject’s front teeth. A 24-year-old female started beating her boyfriend in bed because he “looked so peaceful” and she later attempted suicide. A 29-year-old female struck an acquaintance twice in the face, and then started smashing doors in her own home and beating on her truck.”
Read entire article: http://www.pharmalot.com/2010/07/chantix-and-violence-what-patients-have-in-common/
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Antidepressants the same as placebo “If antidepressants work, why is the prevalence of depression not decreasing?”
The StarPhoenix
By Mark Lemstra
July 22, 2010
We could save $2 billion a year on health-care costs in Saskatchewan while actually improving health outcomes if we adopt evidence-based protocols.
To do so, we need to go line by line through budgets to find about $40 million of efficiencies in each of about 50 areas.
This is the second article in a five-part series on depression. The first one discussed how there is no medical test to diagnose depression; the interview scales have no known validity or reliability because there is no comparative gold standard; the varying interview scales result in different diagnostic conclusions; and almost every life reaction is considered a symptom for depression — including things such as indecisiveness, inability to concentrate, changes in weight or sleeping pattern.
None of this is very scientific.
From 1952 to 1980, the Diagnostic Statistical Manual of Mental Disorders (DSM) described mental disorders as reactions to environmental events such as the death of a loved one.
To make depression seem more medical, the editors of the DSM published a revision in 1980, dismissing environmental influences as causative events.
A small group of practitioners voted and agreed that depression should no longer be diagnosed if the symptoms were caused by factors such as bereavement, substance use or other medical conditions.
Read entire article: http://www.thestarphoenix.com/health/Effect+antidepressants+placebos+similar/3307896/story.html
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The malicious use of pharmaceuticals: An under-recognized form of child abuse
Physorg.com
July 22, 2010
Child abuse is a serious problem that affects nearly one million children a year in the United States alone. The American Academy of Pediatrics and the US Department of Health and Human Services classify child abuse into four categories including neglect, physical abuse, sexual abuse, and emotional abuse. None of these categories, however, clearly includes the abusive use of drugs on children. A study soon to be published in the Journal of Pediatrics investigates the malicious use of pharmaceuticals and attempts to shed light on this under-recognized problem.
Dr. Shan Yin from the University of Colorado and the Rocky Mountain Poison Drug Center at Denver Health reviewed cases of pharmaceutical abuse reported to the National Poison Data System between 2000 and 2008. Dr. Yin included reports of the malicious use of alcohol, painkillers, cough and cold medicines, sedatives and sleeping pills, and antipsychotic medicines.
Of the more than 1400 cases studied, nearly 14% resulted in moderate to major consequences, including death. Nearly one-half of the abused children were exposed to at least one sedative. An average of 160 cases, including two deaths, was reported each year. Motives and legal findings were unavailable for these particular cases; however, motives for the abusive use of drugs generally are varied, and can include punishment, amusement, or a wish for a break from childcare responsibilities.
This study illustrates the seriousness of the abusive use of drugs administered to children.
Read entire article: http://www.physorg.com/news198936684.html
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The New American—Psychiatry’s Brave New World
The New American
By Beverly K. Eakman
July 22, 2010
After some 40 years of psychiatry-based “parenting,” free societies are experiencing behaviors by out-of-control children virtually unknown in the 1950s — first-graders biting and kicking their teachers; adolescents blowing away their classmates; pre-teens cursing, spitting, and vandalizing while adults look on. Advocates for a Nanny State see all this as a wedge to further their controlling agenda. Anyone curious as to where we’re headed need look no further than the United Kingdom’s now-institutionalized ASBO legislation.
In July 1998, the U.K.’s Crime and Disorder Act enacted the “Anti-Social Behaviour Orders” (ASBOs) to tackle disagreeable and disruptive acts. ASBOs are court-ordered restrictions on “unsociable conduct” aimed at youngsters aged 10 or over. Breaching an ASBO is a criminal offense.
Eight years into the legislation, some 12,675 ASBOs had been issued. Nearly 2,000 youngsters, aged 10 to 17, were jailed by 2007 for an average of six months each for breaching ASBOs. Even that was not enough. According to Mail Online, May 27, 2007 (“Revealed: Blair’s secret stalker squad”), the government attempted to widen the definition of “mental disorder” so that the right not to be detained in a psychiatric facility based on cultural, political, or religious beliefs would be forfeited.
By 2007, Britain had gone a long way to becoming the ultimate modern police state. The nation had more than 20 percent of the world’s CCTV cameras incorporating automatic number-plate recognition, facial recognition and “suspicious behavior recognition” software, which analyzes clusters and movements in search of “behavioral oddities.” Some £1 million was allocated for hidden loudspeakers so that camera operators could issue orders, very loudly, to anyone seen littering or committing other “gotcha crimes” (petty rules that are easier to enforce than dangerous acts). A competition was even launched in schools to find “socially conscious” children who might be used for voice-overs to “remind adults to act responsibly on our streets,” according to the U.K.’s Home Office.
“Emotional literacy” classes were introduced in schools to teach children how to manage anger and jealousy and develop empathy and self-motivation. This move mirrors the touchy-feely curricular trends of American classrooms — “conflict resolution,” “survival skills,” “safe sex” and “self-esteem.”
Read entire article: http://thenewamerican.com/index.php/usnews/health-care/4112-psychiatrys-brave-new-world
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Drug maker to settle 200 lawsuits for failing to warn patients of diabetes risks caused by its antipsychotic drug
AboutLawsuits.com
July 23, 2010
AstraZeneca has agreed to settle Seroquel lawsuits filed by about 200 people who claim that the drug maker failed to adequately warn about the risk of diabetes and other side effects of their antipsychotic drug. The Seroquel settlements are reportedly the first payments AstraZeneca has made out of an estimated 26,000 claims that have been presented against the company.
Bloomberg News reports that AstraZeneca has agreed to pay $2 million as a settlement for the Seroquel lawsuits, which comes out to an average of about $10,000 per claim. It is not clear what injuries were involved in these claims, or what the circumstances are for the cases. All of the settled lawsuits involved plaintiffs represented by one attorney, and Bloomberg News reports that the agreement came as a result of court-ordered mediation.
Although AstraZeneca has previously indicated that they would fight all Seroquel cases at trial, company officials now indicate that they will continue to negotiate with plaintiffs’ attorneys.
Seroquel (quetiapine fumarate) is an atypical-antipsychotic that is a top selling drug for AstraZeneca, generating nearly $5 billion a year in sales. Originally approved by the FDA in 1997 for the treatment of schizophrenia, it has been frequently prescribed off-label for uses that were not approved as safe and effective at the time, such as anxiety, obsessive dementia, compulsive disorders and autism.
In July 2006, all Seroquel lawsuits filed in federal courts throughout the United States were consolidated for pretrial litigation before U.S. District Judge Anne Conway in the Middle District of Florida as part of a multidistrict litigation (MDL). In May of this year, Judge Conway determined that the majority of the work in the Seroquel litigation was complete, and began remanding cases back to the original jurisdiction where they were filed for trial.
Read entire article: http://www.aboutlawsuits.com/settlement-for-seroquel-lawsuits-reached-in-some-cases-11647/
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Leading “brain imaging” center (Pharma funded) studying “biology of mental disorders” gets raided by Feds & shut down
The New York Times
By Benedict Carey
July 16, 2010
Columbia University has quietly suspended research at a nationally prominent brain-imaging center and reassigned its top managers after federal investigators found that it had routinely injected mental patients with drugs that contained potentially dangerous impurities.
The investigations found that the center — regarded by experts as the nation’s leader in the use of positron emission tomography, or PET, for psychiatric research — repeatedly violated Food and Drug Administration regulations over a four-year period.
“Failure to promptly correct these violations may result in legal action without further notice,” the agency wrote to Columbia in December 2008, citing lax internal quality control and sloppy procedures for formulating drug injections.
F.D.A. investigators returned in January 2010 and found that many of the center’s lab’s practices had not changed, and cited a long list of specific violations, including one instance in which the staff hid impurities from auditors by falsifying documents.
“They raided the place like it was a crime scene, seizing hard drives,” said one former lab worker, who requested anonymity because he feared reprisals from the university.
In a statement, the university said on Friday that it had conducted its own investigation of the lab at the request of the F.D.A. had and reported to the agency on July 6 that it found no evidence of harm to patients. The F.D.A. did not publicize its investigations; The New York Times learned of them from doctors who were familiar with the lab’s problems.
The office under fire, the Kreitchman PET Center, on West 168th Street in Manhattan, has attracted millions of dollars in research funds from the federal government and pharmaceutical companies to study drug actions and the biology of brain disorders, among other things.
Read entire article: http://www.nytimes.com/2010/07/17/health/17columbia.html
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Psychiatric drug use skyrockets in U.S. military
Natural News
By David Gutierrez
July 26, 2010
Use of prescription psychotropics has skyrocketed among U.S. military personnel in recent years, according to an investigation by Military Times.
At least 17 percent of active-duty military personnel are currently taking an antidepressant, including as many as 6 percent of all deployed troops. In contrast, the rate of antidepressant use in the wider U.S. public is only 10 percent.
Overall, one in six military service members takes at least one type of psychiatric drug. The numbers are probably higher than estimated, since troops are also known to share and trade prescription drugs with each other, even while in combat zones.
Data obtained from the Defense Logistics Agency show that overall use of psychiatric drugs increased by 76 percent between 2001 and 2009. More specifically, use of anti-seizure drugs increased 70 percent, use of sedatives and anxiety drugs increased 170 percent, and antipsychotic use increased 200 percent.
Spending on anticonvulsants increased from $16 million to $35 million per year, spending on anxiety drugs and sedatives increased from $6 million to $17 million, and spending on antipsychotics increased from $4 million to $16 million.
Although antidepressants are among the drugs most commonly taken by military personnel, their use increased only 40 percent between 2001 and 2009. Spending actually dropped by 16 percent, likely reflecting the new availability of less-expensive generic drugs.
According to a 2009 study by the Veterans Affairs Administration, approximately 60 percent of psychiatric drug use by military personnel is for “off-label” uses not approved by the FDA. Thus, antipsychotic drugs intended for the treatment of schizophrenia are now being widely prescribed for post-traumatic stress disorder symptoms such as anger, headaches, nervousness and nightmares.
“Patients may be exposed to drugs that have problematic side effects without deriving any benefit,” said Robert Rosenheck of Yale University. “We just don’t know. There haven’t been very many studies.”
Further compounding concern over side effects, many troops regularly mix two or more drugs together into untested cocktails. The effects of multiple drugs acting in unison have rarely been tested. When both drugs act on the same organ — in this case, the brain — the chance of unforeseen interactions is even greater.
“In the case of poly-drug use — the ‘cocktail’ — where you are combining an antidepressant, an anticonvulsant, an antipsychotic, and maybe a stimulant to keep this guy awake — that has never been tested,” Breggin said.
Among the side effects that some health professionals worry about are impaired motor skills, reduced reaction time, increased suicide risk, irritability, aggressiveness and hostility.
“Imagine causing that in men and women who are heavily armed and under a great deal of stress,” psychiatrist Peter Breggin said.
Read entire article: http://www.naturalnews.com/029285_psychiatric_drugs_military.html
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Government is daring to keep kids on drugs
HeraldTribune.com
By Tom Lyons
Apparently the U.S. Food and Drug Administration had at least heard about the suicide of Gabriel Myers.
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The real reason: He was 7 years old.
Whatever else might have helped lead such a young child toward ending his life, one detail was impossible to ignore: The boy was being treated with three different psychotropic medications.
Medications of that sort make some people more depressed or even suicidal, and their effects when combined are harder to predict, especially in children.
So DCF did a quick check on how many foster children were being given such drugs. Troubling facts emerged.
Not only was the percentage high, it was not really known. And, in more than a third of known cases, required approval permission documents were missing.
DCF Secretary George Sheldon quickly acknowledged the problem and started a study group to learn more and give advice. And a year later, the picture is at least more clear. Very few files lack required documentation now. And when I asked for the most current numbers, they were available, and somewhat lower. In the Sarasota-Manatee-DeSoto county region, 11 percent of foster children are given psychotropic meds. Statewide, it is 13 percent.
Some critics insist too many foster parents, lacking the skill or patience to work with troubled children who arrive as strangers, are still too quick to see medication as the way to curb problem behavior or just keep foster children quiet, no matter the side effects.
But whatever the truth of that, the study group recommended some good changes, and one made sense immediately, I thought: Ban the use of foster kids in drug trials.
Drugs helpful to some adults can react differently in children, who may suffer more extreme and unintended side effects. And so, clinical trials on children are needed, but it it is a scary field of study. The most alert and caring parents are key for monitoring the children during such trials, I would think.
So I was surprised at the FDA’s response when Sheldon wrote to ask how many Florida foster children were involved in drug studies as they bounce from foster family to foster family.
Jill Hartzler, an associate FDA commissioner, responded that the FDA — which oversees the studies to make sure children’s involvement is approved and understood by parents or guardians — didn’t have an exact number. Or even an estimate. The FDA, in fact, doesn’t have the slightest idea how many Florida foster kids are or have been involved in its drug studies.
But that wasn’t the weirdest part. Hartzler and the FDA also urged that Florida not bar foster kids from drug trials, arguing that benefits can outweigh risks.
I’m happy to say Sheldon is not taking that advice. But as he explains his reasoning more tactfully than does Richard Wexler of the National Coalition for Child Protection Reform, I’ll quote Wexler, who says the FDA’s position is absurd.
Myers’ death by hanging happened in a Florida foster home last year, but that wasn’t the main reason it triggered a major reaction at Florida’s Department of Children and Families.
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Incredibly, FDA urged Florida not to bar foster kids from drug trials, arguing “benefits” can outweigh risks.
HeraldTribune.com
By Tom Lyons
Apparently the U.S. Food and Drug Administration had at least heard about the suicide of Gabriel Myers.
<!–
AC = 1234
–>
The real reason: He was 7 years old.
Whatever else might have helped lead such a young child toward ending his life, one detail was impossible to ignore: The boy was being treated with three different psychotropic medications.
Medications of that sort make some people more depressed or even suicidal, and their effects when combined are harder to predict, especially in children.
So DCF did a quick check on how many foster children were being given such drugs. Troubling facts emerged.
Not only was the percentage high, it was not really known. And, in more than a third of known cases, required approval permission documents were missing.
DCF Secretary George Sheldon quickly acknowledged the problem and started a study group to learn more and give advice. And a year later, the picture is at least more clear. Very few files lack required documentation now. And when I asked for the most current numbers, they were available, and somewhat lower. In the Sarasota-Manatee-DeSoto county region, 11 percent of foster children are given psychotropic meds. Statewide, it is 13 percent.
Some critics insist too many foster parents, lacking the skill or patience to work with troubled children who arrive as strangers, are still too quick to see medication as the way to curb problem behavior or just keep foster children quiet, no matter the side effects.
But whatever the truth of that, the study group recommended some good changes, and one made sense immediately, I thought: Ban the use of foster kids in drug trials.
Drugs helpful to some adults can react differently in children, who may suffer more extreme and unintended side effects. And so, clinical trials on children are needed, but it it is a scary field of study. The most alert and caring parents are key for monitoring the children during such trials, I would think.
So I was surprised at the FDA’s response when Sheldon wrote to ask how many Florida foster children were involved in drug studies as they bounce from foster family to foster family.
Jill Hartzler, an associate FDA commissioner, responded that the FDA — which oversees the studies to make sure children’s involvement is approved and understood by parents or guardians — didn’t have an exact number. Or even an estimate. The FDA, in fact, doesn’t have the slightest idea how many Florida foster kids are or have been involved in its drug studies.
But that wasn’t the weirdest part. Hartzler and the FDA also urged that Florida not bar foster kids from drug trials, arguing that benefits can outweigh risks.
I’m happy to say Sheldon is not taking that advice. But as he explains his reasoning more tactfully than does Richard Wexler of the National Coalition for Child Protection Reform, I’ll quote Wexler, who says the FDA’s position is absurd.
Myers’ death by hanging happened in a Florida foster home last year, but that wasn’t the main reason it triggered a major reaction at Florida’s Department of Children and Families.
Read entire article here: http://www.heraldtribune.com/article/20100725/COLUMNIST/7251032/2055/NEWS?p=1&tc=pg
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British psychiatrists warn APA’s new “mental disorders” will turn large numbers of normal people into psychiatric patients
The Press Association
July 27, 2010
A further step in the Americanisation of mental healthcare threatens to turn large numbers of “normal” people into psychiatric patients, British experts warned.
Sweeping changes to a diagnostic “bible” that influences practitioners around the world could make it far easier to be labelled with a psychological problem, it is claimed.
One suggestion of the US authors is a new diagnosis of “psychosis risk syndrome” which singles out people thought to be at risk of developing a psychotic illness such as schizophrenia.
Individuals falling into this category might experience occasional mood changes, feelings of distress, anxiety or paranoia, or fleeting episodes of hearing voices.
In the past they might have been considered difficult or eccentric. Under the new proposals they could receive a diagnosis that affects their future lives and job prospects. Yet they may never develop “full blown” psychosis.
Other diagnoses under consideration include “mixed anxiety depression”, “binge eating, and “temper dysregulation disorder with dysphoria”. In addition, the bar could be lowered on some common existing disorders, such as depression, so that more people are considered to have symptoms that warrant a diagnosis.
Professor Til Wykes, from the Institute of Psychiatry at King’s College London, spoke of a trend that was “leaking into normality”. She said: “It shrinks the pool of normality to a puddle, and there are going to be fewer people who won’t end up having a diagnosis of mental illness.”
Prof Wykes edits the Journal of Mental Health which carries a “health warning” about the proposals in its latest issue. The changes have been put forward for discussion by a powerful group of US experts working on the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5).
Read entire article here: http://www.google.com/hostednews/ukpress/article/ALeqM5gHnD0Z3xJQt8sJ8PEIComLTtomvg
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The BBC—new report challenges psychiatry’s billing bible, the DSM—”Mental Health: Are we all sick now?”
BBC News
By Philippa Roxby
July 28, 2010
Diagnosing psychiatric illness has always been controversial, mental health experts say. Now some are worried that a new draft of the diagnostic ‘bible’ for mental health medicine could result in almost everyone being diagnosed with a mental condition.
The diagnostic ‘bible’ in question is the Diagnostic and Statistical Manual of Mental Disorders, published by the American Psychiatric Association.
The US manual is used worldwide as a basis for diagnosis, research and medical education.
Its forthcoming fifth edition – known in the profession as as DSM-5 – is set to contain a range of new diagnoses, including conditions such as “mixed anxiety depression, psychosis risk syndrome and temper dysregulation disorder”, as well as the more mundane binge eating.
The danger, say experts writing in a special issue of the Journal of Mental Health, is that there has not been enough research to back up these changes.
Even the smallest shift in how to define something like depression could have huge implications.
Self-fulfilling
Dr Felicity Callard, senior research fellow at the Institute of Psychiatry, King’s College London, says it is crucial to understand what happens when people are over-diagnosed.
“There are very big potential implications on how people, particularly adolescents, respond to being told they have a mental illness. It’s likely there will be harmful consequences,” she said.
She cites the “at risk psychosis syndrome” diagnosis as an example of a label which is given to young people who ‘might’ have psychosis – characterised by abrupt changes in personality. It is a diagnosis of something which could result in a disorder, but only potentially. That can have complicated effects, she says.
“Imagine a young person being told that they are “at risk” of developing a mental illness. How would that affect that individual’s behaviour? Could it lead to increased stigma or even discrimination? And how might it affect the parents and family of that person too?”
Jerome Wakefield of New York University’s Department of Psychiatry writes: “One of the most frightening scenarios is the potential for medicating people – particularly children – who haven’t yet shown any signs of illness in a bid to ‘treat’ them.”
These concerns are shared by a number of clinical experts in the Journal of Mental Health.
Read entire article here: http://www.bbc.co.uk/news/health-10787342
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