Archive for August, 2009

Doped Up and Duped – nearly impossible to find independent studies of psych drugs with no Pharma ties

Monday, August 10th, 2009

David Healy
guardian.co.uk
August 8, 2009

Adverse effects of widely-prescribed drugs are often overlooked because there is so little truly independent academic evidence

Since 2005, the SSRI paroxetine, first marketed by GlaxoSmithKline as Seroxat, has carried warnings of risk of birth defects. In the US litigation in which I have been asked to give evidence, the plaintives will argue that, even before they were launched, there was good laboratory evidence that the SSRIs might cause problems, and, following their initial marketing, evidence emerged over a decade ago from clinical use that the drugs actually do cause problems.

Yet these drugs have been actively promoted, de facto primarily to women of child-bearing years. How could this happen?

Part of the problem is that having gone to their GP with a nervous problem, many women become dependent on a prescribed SSRI and find it impossible to stop using it whether they wish to get pregnant or if they find they are pregnant while on treatment. But few, if any, of these women will have been informed of either the risk of birth defects or the risk of becoming addicted. Why not?

What we are seeing here is the astonishing marketing power of pharmaceutical companies, which can now effect huge changes in medical culture within months. In this case, a great part of the scientific literature (the primary marketing tool of companies) on the use of antidepressants in pregnancy and on dependence on antidepressants is ghostwritten – just as virtually all literature on giving antidepressants to children was, at one point, company-written.

Read entire article: http://www.guardian.co.uk/commentisfree/2009/aug/08/seroxat-pharmaceutical-birth-defect

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GPs handing out antidepressants linked to birth defects

Saturday, August 8th, 2009

Sophie Borland
Daily Mail
August 8, 2009

GPs are still prescribing an antidepressant known to cause birth defects in unborn children to thousands of women every year, it emerged last night.

Pills such as Seroxat may result in babies being born with malformed hearts if taken in the first few weeks of pregnancy – a time when many women are still unaware they may have conceived.

Several scientific studies have suggested that the class of drugs known as SSRIs, which also includes Prozac, could double the rate of birth defects.

Seroxat is believed to be prescribed to 4 million people in Britain a year and it has been particularly marketed towards women as a drug to relieve anxiety and depression.

But both the Medicines and Healthcare products Regulatory Authority (MHRA) and the National Institute for Clinical Excellence (NICE) watchdogs have warned of the drug’s potential dangers and urged GPs not to prescribe them to pregnant women unless completely necessary.

Last night leading doctors warned that the pills were still being routinely handed out to mothers-to-be and women of a childbearing age without warning of the risks.

Read entire article:  http://www.dailymail.co.uk/news/article-1205149/GPs-handing-antidepressants-linked-birth-defects.html

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Antidepressants once seen as miracle drugs: now risks are becoming evident – U.S. courts to hear evidence

Friday, August 7th, 2009

Sarah Boseley
The Guardian
August 7, 2009

US courts to hear claims that insufficient attention was paid to dangers to foetus

Since the horror of the Thalidomide scandal in the 1960s, pharmaceutical companies and medicines regulators have been acutely aware of the dangers drugs may pose to the unborn child.

Establishing what the effect of a drug may be on a foetus, however, is no simple task. Companies must rely on animal studies in the early stages of research and hope that the drug will behave in humans in the same way. Trials on pregnant women are rarely carried out, for obvious reasons.

Depression and anxiety became big business for the pharmaceutical industry in the 1990s as doctors became better at diagnosing the problems, exposing a population of over-achieving, highly-stressed, worried-well.

Women, always more willing to see a doctor than men, were a large proportion of those diagnosed and put on SSRIs (selective serotonin reuptake inhibitors) such as Prozac and the British drug Seroxat, known as Paxil in the US. For a while, these seemed to be the new miracle drugs. They were safer than older antidepressants because the severely depressed could not overdose on them.

But in court cases about to begin in the US, it will be argued that insufficient attention was paid to the possible dangers for young women who were pregnant or might become pregnant and more particularly, for their babies.

Read entire article:  http://www.guardian.co.uk/society/2009/aug/07/antidepressants-drugs-health-risk

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Family sues after son born with birth defects; Mother was prescribed antidepressant while pregnant

Friday, August 7th, 2009

Sarah Boseley
guardian.co.uk
August 7, 2009

Kaden Mendoza has just turned seven. His parents, Deborah and Kevin, gave him a big party. They do it every birthday. “It is another year that he has made it through,” says Deborah.

Kaden has undergone open heart surgery three times, the first when he was nine weeks old. “We didn’t find out about Kaden’s heart condition straight away and we almost lost him,” says his mother.

The fourth chamber of his heart was not visible on the ultrasound scan she had when she was pregnant. They didn’t know it was because it was not fully developed. He was two months old when she took the baby to the doctor because he was not breastfeeding.

“His lungs were full of blood,” she says. That was on 22 September 2002. On the 24th, he was airlifted to San Francisco from their home in Washington for his first heart operation.

Throughout her pregnancy, Deborah Mendoza had been taking the antidepressant Paxil, known in the UK as Seroxat. It had been prescribed by the doctor she had seen when she had a panic attack.

Read entire article: http://www.guardian.co.uk/society/2009/aug/07/paxil-seroxat-antidepressants-glaxosmithkline

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Antidepressants & birth defects

Friday, August 7th, 2009

Sarah Boseley
The Guardian
August 7, 2009

Revealed: GPs still prescribing pill, despite evidence of risk in pregnancy

Thousands of women in the UK may be taking antidepressants prescribed by their GPs without knowing that the pills, which are hard to stop taking, could cause birth defects in unborn children.

The problems relate to a class of drug known as SSRIs (selective serotonin reuptake inhibitors), which includes Prozac and, in particular, the British-made Seroxat.

Several studies have shown a link to birth defects, particularly malformed hearts, in a small proportion of the babies born to women who were taking the drug in the early weeks of pregnancy.

Most GPs in the UK believe that these drugs are safer than older antidepressants. Seroxat has been marketed to women as a drug to relieve anxiety and depression.

In the US, the Food and Drug Administration, which licences medicines, issued a warning in 2005 and changed the status of Seroxat, which is sold there under the brand name Paxil. The FDA warns doctors “not to prescribe Paxil in women who are in the first three months of pregnancy or are planning pregnancy, unless other treatment options are not appropriate”.

Read entire article:  http://www.guardian.co.uk/society/2009/aug/07/women-antidepressant-birth-defects

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“The Low-Down on Depression and Mental Illness” by Beverly Eakman, author & former Science Editor at NASA

Thursday, August 6th, 2009

Beverly K. Eakman
The John Birch Society
August 6, 2009

Fox News just informed viewers that 27 million Americans are being treated for depression. The Washington Times ran a three-part series this week on the tsunami of mental illness in New Orleans four years after Hurricane Katrina, mostly depression and post-traumatic stress disorder (PTSD). A rash of additional articles has appeared nationwide on obsessive-compulsive disorder (OCD), including one from last Sunday’s (August 2) Washington Times “Pure suffering for OCD Patients,” by Cheryl Weinstein. All news sources, regardless of political persuasion, lend the aura of medical legitimacy to these phenomena.

But just three years ago, we were hearing a vastly different story: “Cheer up: U.S. not so depressed,” a 2006 Washington Times headline proclaimed, the gist being that reports of epidemic levels of clinical depression were greatly exaggerated — and possibly bogus, along with statistics on alcoholism and anxiety.

The problem — and nearly every news source and medical professional acknowledges it — is that mental illnesses, especially depression, PTSD and OCD, are difficult, if not impossible, to diagnose or quantify.  There is no X-ray, blood test, DNA or other chemical analysis that nails these as bona fide sicknesses, such as one might seek, say, for a brain injury or diabetes. And while there is little question that people do suffer from acute, long-term sadness, stress and compulsive behaviors, there exists no direct, medical proof for the notion of biologically-based brain disorders, contrary to the claims of pharmaceutical companies and mental-health advocacy groups like the National Alliance on Mental Illness (NAMI).

What that means for average citizens is that there is no magic bullet, no medication, to “cure” what are essentially human phenomena, not medical conditions.

Read entire article:  http://www.jbs.org/jbs-news-feed/5190

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Suicide Prevention Drug Pushing Racket: Drug company shills publish bogus studies to promote antidepressants

Thursday, August 6th, 2009

Evelyn Pringle
Natural News
August 6, 2009

Nearly every year, as part of the suicide prevention drug pushing racket, drug company shills publish a bogus study with claims that more people are dying from suicide due to a black box warning of an increased risk of suicide in young people on the labels of SSRI and SNRI antidepressants.

Although the FDA did announce that the black box warnings, for children under 18, would be added to antidepressants in October 2004, the warnings were not on the labels until the spring of 2005. The extended warnings, to include young persons through age 24, were not added until mid-2007.

This year’s bogus study was announced on June 2, 2009, with a WebMD headline asking: “Are Antidepressant Warnings Causing Harm?” The study titled, “Persisting Decline in Depression Treatment After FDA Warnings,” was published in the “Archives of General Psychiatry,” with claims that there has been a drastic drop in the diagnosis of depression in both children and adults.

“Policy actions are required to counter the unintended consequences of reduced depression treatment,” the authors wrote in the study.

Prescriptions written for antidepressants also have dropped significantly, and these “unintended” consequences of the FDA’s warnings are continuing, the junk science co-author of the study, Robert Valuck, PhD, of the University of Colorado Denver’s School of Medicine, told WebMD.

Read entire article:  http://www.naturalnews.com/026789_suicide_suicide_prevention_Eli_Lilly.html

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How Many of the 27 Million Americans on Antidepressants Actually Have Undiagnosed Thyroid Disease?

Wednesday, August 5th, 2009

Mary Shomon
About.com
August 5, 2009

According to news reports out today, the use of antidepressants doubled between 1996 and 2005. Today, 10% of the population is taking antidepressant medication — that’s an estimated 27 million Americans.

The question this raises for me is, how many of these people who have been diagnosed as “depressed” — usually by primary care and family doctors — are actually hypothyroid, but haven’t been properly tested and diagnosed? How many of the people taking antidepressants may actually be misdiagnosed?

It’s an important question. Because we know that depression can be a symptom of hypothyroidism. And we also know that there appears be a relationship between autoimmune thyroid disease/thyroid antibodies and depression. And we know that thyroid treatment can sometimes help as an adjunct to treatment for depression.

Consider the scenario. A woman goes to the doctor, complaining that she’s feeling more tired than usual lately. She’s gained a few pounds. And she feels down in the dumps, a bit blue and moody. Does the doctor think, “Hmm, fatigue, weight gain, depression — these could be signs of hypothyroidism. Let me run a complete thyroid panel?” Sometimes. But more often, (more…)

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The real lowdown on Antidepressants: All Doped Up

Wednesday, August 5th, 2009

R. Cort Kirkwood
The New American
August 5, 2009

Between 1996 and 2005, Reuters reports, the use of anti-depressants doubled to nearly 10 percent of the American population. In 1996, the figure was 13 million. Now, it’s 27 million.

Those numbers, obviously, should cause some worry.

For one thing, the suicide rate for middle-aged people is rising, Reuters reported, suicide being a risk factor in taking antidepressants. According to the Journal of Preventative Medicine, the suicide rate for middle-aged Americans increased 16 percent from 1999 to 2008, which roughly coincides with the massive increase in anti-depressant use.

Indeed, such is the risk for suicide that each container carries a “black box warning.” The Food and Drug Administration issued the mandate to carry the warning in 2007. Studies had shown the drugs increased the risk of suicide in teens and children. Clearly, as the psychiatrist quoted for the Reuters piece suggested, they might just increase the risk for the middle-aged as well.

For another thing, while these folks, most of them baby boomers, are usually killing only themselves, their children aren’t. The baby boomers’ kids take others with them before they commit suicide.

Recall that several of the notorious school shooters were taking such medications, most notably Eric Harris, one of the two shooters at Columbine High in Colorado. Harris and his partner, Dylan Klebold, slaughtered 12 students and a teacher, while injuring 21, before killing themselves. Harris was taking Luvox.

Read entire article:  http://www.thenewamerican.com/index.php/usnews/health-care/1595

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PR Web: CCHRInt Announces FDA Reported Psychiatric Drug Side Effects Search Engine

Tuesday, August 4th, 2009

Citizens Commission on Human Rights International Announces FDA Reported Psychiatric Drug Side Effects Search Engine: Decrypted FDA reports reveal 4,260 suicides, 2,452 additional deaths, 195 homicides from 2004-2006 alone

Los Angeles, CA (PRWEB) August 4, 2009 — For the first time the side effects of psychiatric drugs that have been reported to the U.S. Food and Drug Administration (FDA) by doctors, pharmacists, other health care providers and consumers have been decrypted from the FDA’s MedWatch reporting system and been made available to the public in an easy to search psychiatric drug side effects database and search engine.  The database is provided as a free public service by the mental health watchdog, Citizens Commission on Human Rights International (CCHR).

The report totals reveal that between 2004-2008 the FDA’s MedWatch system received pregnancy-related psychiatric drug adverse reaction reports which included 2,442 babies born with heart disease, 3,372 other birth defects, as well as 1,072 miscarriages, abortions and other deaths.

The database also reveals that, between 2004-2008 there were reports submitted to MedWatch including 4,895 suicides, 3,908 cases of aggression, 309 homicides and 6,945 cases of diabetes from people taking psychiatric drugs. These numbers reflect only a small percentage of the actual side effects occurring in the consumer market, as the FDA has admitted that only 1-10% of side effects are ever reported to the FDA.

The database is searchable by individual reports (for the 2004-2006 period), type of drug, age of patient, the side effect reported (suicide, homicide, heart attack, stroke, mania, etc.), and whether the drug in question carries a black box warning (the agency’s strongest warning–short of banning a drug).

It is searchable by drug name and age group and includes who reported the psychiatric drug reaction (doctor, pharmacist, consumer, etc.). It also includes the top 20 reported adverse reactions to all psychiatric drugs to the FDA and combined summaries of all psychiatric drug reactions for the years 2004-2006 and 2004-2008.

Read entire article: http://www.prweb.com/releases/CCHR-Psychiatric-Drug/Effects-Search-Engine/prweb2714464.htm

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