Zantac Lawsuit


Researching drug company and regulatory malfeasance for over 16 years
Humanist, humorist

Monday, December 08, 2008

PHARMAGREED DISORDERS

ACS - ALARM CLOCK SYNDROME: [Cannotwakeupalitis]
People with Alarm Clock Syndrome fail to set their alarm clocks at night thus over sleeping in the morning. Even if they remember to set their alarms they have a tendency to sleep through the alarm or lean across to hit the snooze button.

NPS - NOSE PICKING SYNDROME: [Boogerhausen Disease]
People often seen picking their noses for no apparent reason, they can be witnessed at dining tables, on buses, trains etc. Severe cases of Nose Picking Syndrome sees the patient rolling the contents of their nose into a small ball and either flicking it, rubbing it on the carpet or in extreme cases, on the curtains.

FTS - FOOT TAPPING SYNDROME: [Danceophobia]
Foot Tapping Syndrome was first diagnosed by Prof Baron Von Littlesence in America in the late 1940's and early 1950's. The patient feels an overwhelming urge to tap their foot along to the rhythm of rock n' roll music. Severe cases sees them shaking their hips. Elvis Presley had severe Foot Tapping Syndrome.

CES - CLOSED EYE SYNDROME: [Tootiredulitis]
The patient shows abnormal behaviour usually during the period of darkness, on average after 10pm. In most cases they are seen to open their mouths and let out strange sounds. This is usually followed by a feeling of tiredness. The patient will, in most cases, shut their eyes and be unable to hold conversations for sometimes quite lengthy periods. Rip Van Winkle had severe Tootiredulitis.

Although sometimes disabling and frustrating the above disorders can be cured. Pharmagreed was founded in 1980 and are one of the biggest pharmaceutical companies in the world. Our motto is 'IF YOU CAN'T FIX IT...WE CAN'.

All of our drugs have been clinically tested and pass all FDA and MHRA standards. Esteemed psychiatrists have worked alongside us so we can help you with these debilitating disorders.

Ask your doctor for ShitabrickTM, the miracle pill from Pharmagreed.

*ShitabrickTM may cause dizziness, drowsiness and a dry mouth.


Fid










Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
CHIPMUNKA PUBLISHING

AVAILABLE FOR DOWNLOAD HERE


PAPERBACK COMING SOON

Yesterday was a good day :-)

Some of you know I'm an Aston Villa supporter, they are doing pretty well in the Premiership so far this season. Yesterday they played Everton away. These are the condensed highlights of what was an edge of the seat game.

For my American viewers: Football is played with the feet and a round ball :-)

Enjoy... I did

Fid






Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
CHIPMUNKA PUBLISHING

AVAILABLE FOR DOWNLOAD HERE


PAPERBACK COMING SOON

DEMONIC



Fid


Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
CHIPMUNKA PUBLISHING

AVAILABLE FOR DOWNLOAD HERE


PAPERBACK COMING SOON

Sunday, December 07, 2008

DID THEY [GSK] REALLY SAY THIS?




Fid


Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
CHIPMUNKA PUBLISHING

AVAILABLE FOR DOWNLOAD HERE


PAPERBACK COMING SOON

Saturday, December 06, 2008

Drip Drip Drip - Paxil Info Leaks Out

One of the best articles ever written regarding Paxil [Seroxat] and GlaxoSmithKline. It was written 2 years ago by Evelyn Pringle, a writer who pulls no punches. If there was any justice in this world, Evelyn would get a Pulitzer for this brilliant article.

Drip Drip Drip - Paxil Info Leaks Out

By Evelyn Pringle

Secrecy agreements in litigation hide information about defective products or a company’s negligence, and sometimes go so far as to prohibit the parties from discussing that there ever was a lawsuit. Such is the case with Paxil and as a result, unwitting patients continued to take the drug long after its dangers were known to GlaxoSmithKline.

Many lawsuits filed against Glaxo have been settled out of court, with confidential agreements that prevent the public from knowing about the harmful effects of the Paxil.

Previously sealed documents and internal company memos suppressed with protective orders, prove that Glaxo knew about the problems with Paxil before it received FDA approval, but continued to sell the drug for over a decade without warning consumers.

Long overdue legislation is currently pending in both the US House of Representatives and the Senate known as Sunshine in Litigation Act of 2005, which basically says that a court shall not enter an order restricting the disclosure of information obtained through discovery, an order approving a settlement agreement that would restrict the disclosure of such information, or an order restricting access to court records in a civil case

Glaxo currently faces thousands of lawsuits over Paxil side effects related to addiction, dependence, and a severe withdrawal syndrome.

SSRIs (selective serotonin reuptake inhibitors) like Paxil, are not addictive in the sense that “an individual would mortgage their livelihoods and all they hold dear for further supplies of the drug,” according to Dr David Healy MD, FRCPsych, North Wales Department of Psychological Medicine

SSRIs can hook patients in the sense of making you “physically dependent,” he explains.

Dr Healy, is considered an expert on Paxil and has had access to confidential studies from the Glaxo archives. The common symptoms of withdrawal, he says, break down into two groups. The first group may be unlike anything you have had before, he warns, to include:

Dizziness Headache Muscle Spasms Tremor Electric Shock-like Sensations Other Strange Tingling or Painful Sensations Nausea, Diarrhoea, Flatulence Dreams, including Vivid Dreams Agitation

The second group overlaps with general nervousness, Dr Healy says, and may lead to you or your physician to think that all you have are features of your original problem. These symptoms include:

Depression Lability of Mood Irritability Agitation Confusion Fatigue/Malaise Flu-like Feelings Insomnia or Drowsiness Mood Swings Sweating Feelings of Unreality Feelings of being Hot or Cold

These symptoms appear in anywhere between 20% to 50% of patients taking SSRIs, Dr Healy says, sometimes within hours of the last dose.

In the class action case against Glaxo settled in 2005, In re: Paxil Products Liability Litigation, MDL No 1574, CD Calif, the plaintiffs were forever silenced by a strict confidentiality clause incorporated into the settlement agreement.

This author obtained a copy of the lawsuit’s complaint, dated August 23, 2001, as well as a copy of the settlement agreement with a secrecy clause that states in relevant part:

Plaintiffs and their attorneys, “will not make any statements, either directly or indirectly, by implication or innuendo, to anyone, including but not limited to consultants, experts, the press or media, concerning the amount or other terms of such settlement or settlements, or the nature and substance of settlement negotiations, or describing or characterizing the settlement in any way.”

Plaintiffs and their attorneys “will not, either directly or indirectly, publicize the fact of the settlement and that any inquiry into the settlement, its amount, meaning, interpretation or comparative value, or the negotiations leading to the settlement by anyone, including but not limited to the press or media, will be met only by a statement that the case has been resolved, and will decline any requests for interviews by the press or media regarding the settlement, its history or its terms.”

The clause even extends the internet specifically in that plaintiffs and attorneys “will not maintain and instead will discontinue any website references to Paxil discontinuation or withdrawal.”

And, it says, they “agree to refrain from any future internet postings regarding Paxil discontinuation or withdrawal.”

Paragraph 5 of the lawsuit’s complaint says that over a 2 years period, “plaintiffs' attorneys have been individually contacted by approximately 500 Paxil withdrawal victims.”

And, the pain and suffering experienced by each individual is the direct result of Glaxo’s “failure to warn users of Paxil’s addictive nature, the drug's inducement of physical or psychologic dependency, and its infliction of dependency/withdrawal syndrome when the patient's Paxil dosage is reduced or terminated,” the complaint states.

Paragraph 16, lists withdrawal reactions that “can summed up as one or more of the following complaints: jolting electric "zaps," dizziness, light headedness, vertigo, incoordination, gait disturbances, sweating, extreme nausea, vomiting, high fever, abdominal discomfort, flu symptoms, anorexia, diarrhea, agitation, tremulousness, irritability, aggression, sleep disturbance, nightmares, tremor, confusion, memory and concentration difficulties, lethargy, malaise, weakness, fatigue, paraesthesias, ataxia, and/or myalgia.”

Paragraph 7, says: “These reactions are "unexpected" to the victims and even their physicians because the manufacturer has deliberately failed to properly warn of this.”

“Both physician and patient unwittingly use Paxil without knowing the drug's addictive traits,” the complaint says.

Paragraph 8, charges that because Glaxo has suppressed the information, patients and physicians are fooled into thinking that the reactions are caused by another condition, such as relapse into depression, thus prompting incorrect and unnecessary medical treatment, including increased dosages of Paxil.

While researchers have acknowledged the potential for withdrawal reactions with all SSRIs, Paxil is by far the worst. Citing data from the World Health Organization, the lawsuit’s complaint states: “Paxil has the highest incidence rate of withdrawal adverse experiences of any antidepressant drug in the world.”

Starting in December 2001, Glaxo finally added a minimizing precaution to Paxil’s label of some possible "discontinuation" side effects affecting "2 percent or greater" of patients based on studies.

However, documents reveal that Glaxo has always known about the withdrawal syndrome. For instance, in 1993, in a report that occurred 5 months after Paxil arrived on the market, Stoker and Eric noted Paxil withdrawal at the American Psychiatric Association's annual meeting in San Francisco, May 22-27, 1993.

The authors of the study conducted 2 week tapering off periods for 186 patients in 6 to 12 week doubled blinded comparative studies. Low dose and high dose groups were studied. Paxil's low dose group actually did worse than the high dose group, suffering 42% withdrawal rate, compared to 38% in the high dose group. And, both occurred even though the tapering off regime was initiated during dosage reduction.

The lawsuit’s complaint specifically describes close to 10 studies that reveal a high rate of withdrawal symptoms since Paxil came on the market that Glaxo was fully aware of.

A fact well-evidenced in internal company documents. A previously suppressed, May 1, 1997, Glaxo memo to, “Paxil Selling Team,” on the “discontinuation syndrome,” defines the withdrawal syndrome as, "a class effect that can occur when an SSRI is stopped abruptly. Symptoms may include asthenia, flu-like symptoms, fatigue, dizziness, nausea, and sleep disturbances (insomnia, vivid dreams or nightmares)."

However, the memo instructs Glaxo sales representatives to avoid using the term and says: "instead of 'withdrawal syndrome,' which implies addictive properties, try to refer to this phenomenon as 'discontinuation symptoms.'"

Eight months later, in a December 1, 1997, "Business Plan Guide," sales representatives were instructed to "minimize concerns surrounding discontinuation symptoms," and told to explain to doctors that the "discontinuation incident rate is two in 1,000 patients."

However, according to a 1997 review, one study found that 25% of patients experienced at least one discontinuation symptoms, verses 5.9% taking a placebo. In another study of patients with major depression, 42% experienced at least 1 discontinuation symptom.

Another internal memo kept hidden with a protective order, states: “Discontinuation: why this is an issue,” followed by, “’97 Seroxat/Paxil sales to end Sept already exceed $1 Billion“.

This particular memo carries a cartoon-like picture of a big black money-bag.

In Paxil literature, Glaxo flat-out lied to patients and specifically said that the drug was not addictive. For example, a pamphlet made available at doctors’ offices and disseminated to patients, asked the question: “Is Paxil addictive?”

The pamphlet then states: “Paxil has been studied both in short-and long-term use and is not associated with dependence or addiction.”

The withdrawal syndrome is real and in fact, it is now known that infants of women who take SSRIs in the last 3 months of pregnancy, may experience symptoms of withdrawal, including convulsions, according to a study published in the February 4, 2005 issue of the journal Lancet.

In addition, experts warn against the use of Paxil and other SSRIs with children. According to Fred Baughman Jr, MD, an adult and child neurologist in private practice for 35 years, "most antidepressants have not proved effective in treating depression in children and some studies suggest they may cause some children to become acutely suicidal.”

Yet in 2002, Dr Baughman says, “nearly 11 million prescriptions for the drugs were given to children, 2.7 million of them to children under 12."

A report by an expert witness, previously sealed with a protective order, reveals how Glaxo concealed and manipulated data concerning Paxil-induced suicidality and how suicide attempts in studies by patients on Paxil were underreported and attempts by people taking a placebo were inflated.

Excerpts from the report were published by psychiatrist, Peter Breggin, MD, in Ethical Human Psychology and Psychiatry, (Volume 8, Spring 2006, pp. 77-84). Dr Breggin is a founder of the International Center for the Study of Psychiatry and Psychology (ICSPP) and the author of the Antidepressant Fact Book (2001).

His report also documents how Glaxo hid the incidence of akathisia (agitation with hyperactivity) and stimulation, which he says, are known risk factors for suicidality and violence.

Dr Breggin’s original report was based on a 3-day review of Glaxo’s sealed files, and was written for the California case of Lacuzong v GSK, and attached to a July 21, 2001, affidavit submitted in a case filed by the widow of a man who drowned their two children and himself in a tub after taking Paxil for three days.

At Glaxo’s insistence, the report remained sealed. However, in the more recent case of Moffett v Glaxo, in the US District Court for the South District of Mississippi, the report was filed in the public record.

“The drug companies,” says Dr Breggin, “settle almost all legal cases brought against them in order to seal incriminating scientific data.”

“The publication of a previously sealed medical expert report is a rare event,” he explains, “the first in my experience.”

In the book, The Antidepressant Solution, author Dr Joseph Glenmullen, a clinical instructor in psychiatry at Harvard Medical School, recommends tapering off antidepressants by following a 5-Step Antidepressant Tapering Program, to reduce both the incidence and severity of withdrawal reactions.

“Research has shown that when patients stop antidepressants cold turkey they can have high rates of withdrawal reactions,” Dr Glenmullen advises, “which vary depending on the particular drug.”

“In studies involving hundreds of patients, 66 percent of patients stopping Paxil,” he says, “have withdrawal reactions.”


*************


Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
CHIPMUNKA PUBLISHING

AVAILABLE FOR DOWNLOAD HERE


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Glaxo Hiding Data... AGAIN!"

This from the excellent blog - Clinical Psychology and Psychiatry: A Closer Look

GlaxoSmithKline, manufacturer of lamotrigine (Lamictal), the antiepileptic drug used widely for bipolar disorder, happily hid clinical trial results which found Lamictal was no better than a placebo. Given recent findings about how often pharmaceutical companies selectively push positive results to publication in medical journals while suppressing negative results, this can hardly be considered a surprise. It is nonetheless instructive to examine how the published data on Lamictal paint a much rosier picture of the drug's efficacy compared to unpublished data.

Nassir Ghaemi, a psychiatrist at Tufts University Medical Center, dug through GSK's online database of information, and found that several negative Lamictal studies (studies which failed to show a benefit for Lamictal over placebo on the primary outcome measure) were quietly residing on the site. Why did GSK post such information on their site? Not out of the goodness of their hearts; rather, because they were forced to post data about clinical trial outcomes as a result of a legal agreement. Here's what Ghaemi found in GSK's database:

FULL ARTICLE HERE



Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
CHIPMUNKA PUBLISHING

AVAILABLE FOR DOWNLOAD HERE


PAPERBACK COMING SOON

Mothers Act Promotes Pregnancy as Cottage Industry

New Article by Evelyn Pringle.

Mothers Act Promotes Pregnancy as New Cottage Industry

By Evelyn Pringle

Women of childbearing years represent the most lucrative market for the makers of psychiatric drugs. The knowledge that infants were being born with birth defects and suffering a withdrawal syndrome when these drugs were used during pregnancy was hidden for decades. Knowledge of these terrible risks would have caused a major drop in sales to this customer base.

Ever since the warnings about birth defects started trickling out a few years ago, the drug companies apparently have been plotting to find ways to reverse their negative impact. But the most sinister plot ever developed is a bill moving for approval in the US Senate right now called the "Melanie Blocker-Stokes Mother's Act," to set up the screening of all pregnant women for mental illness.

The bill is promoted under the ruse of screening for postpartum depression. But a true picture of the target population of this massive drug pushing scheme is evident in the propaganda submitted to support the passage of the original bill in the US House of Representatives and the programs already in place in various states.

The legislation was first introduced in the House in January 2007 by Illinois Democrat Bobby Rush. Under "Background and Need for Legislation," House Report 110-375 states in part:


"Depression is twice as common in women as it is in men, with its peak incidence during the primary reproductive years--ages 25 to 45. Because women are more likely to experience depression during these years, they are especially vulnerable to developing depression during pregnancy and after childbirth."
In February 2007, the "Postpartum Mood Disorders Prevention Act," was introduced in Illinois. The orchestrated attempts to pass this bill included planting reports in the media with claims that pregnant women are at risk for a whole list of mental disorders. For instance, on March 1, 2007 an article in the Naperville Sun stated:


"New moms face increased risks for not only postpartum depression, but also bipolar disorder, schizophrenia, obsessive-compulsive disorder, anxiety and other disorders, according to one of the largest studies of psychiatric illness after childbirth."
The websites set up by the industry-backed front groups supporting the Mother's Act have links to programs that claim new mothers need to be screened for "postpartum" depression, bipolar disorder, schizophrenia, psychosis, anxiety disorder, panic disorder, obsessive-compulsive disorder, post traumatic stress disorder, and eating disorders.

When extending the drug-net to all pregnant women, the groups omit the term "postpartum" and claim women need to be screened for "perinatal" (which means both before and following birth) disorders. In December 2007, Illinois enacted "The Perinatal Mental Health Disorders Prevention and Treatment Act," with the stated purpose "to increase awareness and to promote early detection and treatment of perinatal depression."

But here again, the mention of "depression" only is deceiving because the websites of hospitals in Illinois show they are screening for the entire gamut of disorders mentioned above. Advocate Good Samaritan Hospital in Downers Grove offers "Perinatal Depression Support Services."

"Any woman who is thinking about becoming pregnant, is pregnant, or had a baby within the past year can be affected by depression or other mood disorders," their website says.

"Mental health screening under the guise of identifying individuals who are impaired from some supposed mental disturbance is typically simply another front for pharmaceutical marketing," according to Dr Bose Revenel, co-author with psychologist John Rosemond of the new book, "The Diseasing of America's Children."

"Most are funded or the initiative is provided via pharmaceutical companies and medications are typically promoted as a supposed ‘solution,’" he says.

"The problem here is that, among other things, the drugs promoted have been shown to have potentially serious side effects and their effectiveness compared to placebo only trivial," Dr Revenel reports.

"Furthermore," he says, "the campaign ignores safe and potentially effective interventions such as dietary and nutritional changes and supplements as well as cognitive therapy - all of which are completely free of potential adverse effects, with effectiveness that rivals or exceeds that of the drugs."

"If the screening only picked up women likely to benefit from treatment, then maybe it would be justified," says Dr David Healy, a leading expert on psychiatric drugs from the UK and author of "The Creation of Psychopharmacology."

"But screening will pick up a quarter or a third or more of all pregnant women and will lead to many of these being treated who do not need treatment," he warns. "Over 25% of women might be diagnosed where very few of those are likely to need treatment."

Although no psychotropic drug has FDA approval for use during pregnancy, the recommended treatment for all these so-called "disorders" consists of the newest most expensive antidepressants, antipsychotics, and anticonvulsants. The common practice is to prescribe three or four different drugs at a time for years on end.

The antipsychotics that will benefit as a result of the Mother's Act include Seroquel by AstraZeneca, Risperdal marketed by Janssen, a division of Johnson & Johnson, Geodon by Pfizer, Abilify from Bristol-Myers Squibb, Novartis' Clozaril, and Eli Lilly's Zyprexa.

Lilly also sells two antidepressants, Prozac and Cymbalta, and Symbyax, a combination of Zyprexa and Prozac. The other SSRI (selective serotonin reuptake inhibitor) and SNRI (selective norepinephrine reuptake inhibitor) antidepressants include GlaxoSmithKline's Paxil and Wellbutrin, Pfizer's Zoloft, Celexa and Lexapro from Forest Labs, Luvox by Solvay, and Wyeth's Effexor.

Pregnancy as a cottage industry

New Jersey Democrat Robert Menendez is the lead sponsor of the Mother's Act in the Senate. New Jersey is home to a long list of drug companies. The bill was first introduced in May 2007, but was stuck in committee until Senate Majority Leader Harry Reid introduced an $11 billion omnibus package called "Advancing America's Priorities Act." Senator Reid tried to get the Act passed on July 22, 2008 by slipping it in the omnibus, but failed.

The Act is supported by a drug-funded coalition bent on turning pregnancy into a cottage industry. On September 25, 2008, Susan Dowd Stone, a member of "Postpartum Support International (PSI)," self-described as the "bill’s lead organizational sponsor," issued a Legislation Update, obviously to pump out propaganda through the internet.

“Hundreds of thousands of women across the country suffer at the hands of postpartum depression every year, and they deserve better than the ideological games being played with legislation intended to bring them relief,” Senator Menendez declares in the Update.

"This is a cause I am committed to seeing through, and I will continue to stand up on behalf of mothers suffering from this condition until the blockade is cleared," he vows.

"We will again await its inevitable passage at the next Congressional session when reason may more strongly prevail," Ms Stone writes in the Update.

A gal named Katherine Stone runs the “Postpartum Progress” blog, described as the "most widely-read blog in the United States on these illnesses." She serves on PSI’s board of directors as the public relations outreach chairwoman.

Her blog provides links to the "Top Women's PPMD Treatment Programs & Specialists." Dr Shari Lusskin is listed as a "top" specialist. She is an advisory council member for PSI. On her website under "Pregnancy-related Mood Disorders," the standard talking point about "pregnancy related mood disorders" being prevalent is restated as follows:


"Panic Disorder, Generalized Anxiety Disorder, Obsessive Compulsive Disorder, and Eating Disorders may also develop or worsen during pregnancy and postpartum. Women with Bipolar Disorder, Schizophrenia, or Schizoaffective Disorder are particularly vulnerable during pregnancy and postpartum."
A May 28, 2005 presentation brochure shows Dr Lusskin is a paid speaker for Glaxo, AstraZeneca, Pfizer and Wyeth.

The postpartum blogs are also used to sell books written by the "experts" and promote drug company funded conferences. For instance, on May 13, 2008, Postpartum Progress put out an ad for a June 25, 2008 conference at the University of Minnesota, titled, "Motherhood, Mood Disorders & Anxiety: Before & After Pregnancy." The listed sponsors included AstraZeneca and the National Alliance for Mental Illness (NAMI), the most notorious industry backed front group on the planet.

Eli Lilly is logically the top giver to NAMI and many other front groups because it has the most drugs to peddle. Several class action lawsuits currently filed against Lilly specifically allege that Lilly funneled money to NAMI to aid in the off-label marketing of Zyprexa.

Between 2003 and 2005, Lilly donated $3 million to NAMI, according to the May 28, 2006 Philadelphia Inquirer. Lilly's disclosure records show NAMI groups received more than $700,000 from the company in the first quarter of 2008. NAMI's 2007 Annual Report lists Abbott Labs, AstraZeneca, Bristol-Myers, Eli Lilly, Forest Labs, Glaxo, Janssen, Pfizer, Wyeth and Solvay as "Corporate Partners."

The NAMI website reports that the “National Depression Screening Day” and the “Stop a Suicide Today” campaign are endorsed by the American Psychiatric Association and are conducted in partnership with the American Association of Suicidology, Suicide Prevention Action Network USA, the National Suicide Prevention Lifeline, Suicide Prevention Resource Center, and Mental Health America.

In 2006, the pharmaceutical industry accounted for about 30% of the American Psychiatric Association’s $62.5 million in financing, according to the July 12, 2008 New York Times. Lilly's first quarter grant report for 2007 shows Lilly provided the APA with two grants worth over $412,000. The Suicide Prevention Action Network received $10,000 from Lilly in the first quarter of 2007.

Mental Health America's annual report shows the group received over $1 million from Bristol-Myers, Lilly and Wyeth in 2006. Janssen and Pfizer gave between $500,000 and $1,000,000, and AstraZeneca and Forest Labs donated between $100,000 and $499,000. Glaxo gave the group between $50,000 and $100,000 in 2006.

Other funding sources listed on the MHA website include three treatment centers for eating disorders with links to their websites. The National Association of Anorexia Nervosa and Associated Disorders estimates that the average cost of private inpatient treatment is $30,000 or more a month, according to an April 27, 2006 report by Women's enews.

On May 21, 2008, the president of the Depression and Bipolar Support Alliance (“DBSA”), Sue Bergeson, posted a message on Bipolarconnect.com, saying Illinois Senator Dick Durbin's office had called to say they were having "a hard time making headway" with the Mother's Act. She informed readers that "more than 800,000 women will develop a diagnosable postpartum mood disorder this year! And this number doesn't include the 7.5% of women who will develop major depression during pregnancy."

At the end of the article, Ms Bergeson provided a link and urged people to take "30 seconds" to send a letter to their Senators.

The 2006 Annual Report of DBSA shows AstraZeneca gave the group more than $500,000 in 2006. Companies that donated between $150,000 and $499,000 include Abbott, Bristol-Myers and Wyeth. Forest Labs, Glaxo, Janssen, Pfizer, and Shire Pharmaceuticals each gave between $10,000 and $149,000. Lilly is listed in the section titled, "Matching Gift Companies," in the report.

Battle lines drawn

A number of influential advocacy groups have come out against the Act including the International Center for the Study of Psychiatry and Psychology; Alliance for Human Research Protection; International Coalition For Drug Awareness; Law Project for Psychiatric Rights, Mindfreedom International, AbleChild, and the National Association for Rights Protection and Advocacy.

The website, UniteForLife.org is run by Amy Philo, the Texas mother at the forefront of the "Unite for Life" campaign against the Act. Amy's story provides a poster perfect example of what will happen to hundreds of thousands of women all over the county if the bill is passed.

Amy was labeled mentally ill and told she needed to be on drugs by a nurse making a home visit simply because she got very upset after watching her first-born infant almost choke to death a few days after he was born.

When she followed the nurse’s advice and went to the doctor, the Ob-Gyn would not even take two minutes to listen to Amy talk about what had happened or allow her to explain why she was experiencing such over-whelming fear and anxiety.

Instead of viewing this young mother’s reaction to the near-death of her infant as a normal response, the doctor told her she had a panic attack and sent her home with samples packets of the antidepressant, Zoloft, to prevent postpartum depression, apparently expecting her to get over her traumatic experience by taking a pill.

There were no warning labels on the samples and the doctor did not alert Amy to any of the potential side effects. "He told me Zoloft was perfectly safe for me and the baby and it would make my baby happy too," she recalls.

Within three days, the Zoloft pushed Amy into a state where she started having thoughts of first killing her baby and later of killing her husband, her mother, herself and even her pets. When Amy confessed to having these thoughts, instead of recognizing the side effects of Zoloft and stopping the drug, the medical professionals upped the dose, locked her up in a mental ward away from her baby, and tried to add Zyprexa, to the mix.

They never told Amy why they wanted her to take Zyprexa, but the sheet they gave her said it was for schizophrenia, she recalls. Amy refused to take it because she wanted to nurse and was afraid the drug would harm the baby.

She finally lied her way out of the hospital by claiming she no longer had the bizarre thoughts because she wanted to be with her baby and family. But in reality, Amy battled the obsession with suicide and homicide for months waiting for Zoloft to work.

"The constant ideas of homicide were followed by thoughts of suicide to protect my son from me," she says. "I never had thoughts like this in my life before I took Zoloft."

They also tried to get Amy to take the sleeping pill, Ambien, the anti-anxiety drug, Klonopin, and Celexa, another antidepressant, even though she was nursing. "I always just said no to those," Amy says.

The Ob-Gyn told Amy that she might have to remain on Zoloft for life and without the drug she was not in control enough to have more children. The pediatrician told her, "what's really scary is that PPD seems to get worse each time and you have a 90% chance of getting it after your next baby," she recalls.

She finally quit taking the Zoloft against medical advice and the obsessive thoughts of homicide and suicide stopped and never returned. Amy and her husband have since had a second child with no problem whatsoever without the Zoloft.

She recently obtained copies of her medical records, which show she was labeled with obsessive-compulsive disorder and major depression. Those stigmatizing labels will remain in her records forever with no acknowledgment that Zoloft caused the ordeal.

"Antidepressant-induced mania commonly results in a false diagnosis of a new disorder leading to stigmatization and a possible lifetime of unnecessary, harmful treatment with drugs," says Dr Peter Breggin, author of the new book, "Medication Madness," and the man often referred to as the "conscience of psychiatry."

Drug companies have a big financial incentive to promote these drugs. According to DrugStore.com, a 30-day supply of 20 mg Zyprexa costs $725.93. A 30-day supply of 100 mg Zoloft is $104.84. Klonopin costs $65.93 for 30-days of 2 mg tablets. The price of a 30-day supply of 10 mg Ambien is $145.99, and 20 mg Celexa costs $96.99 for 30-days. Amy’s two-day stay in the mental ward cost her family's insurance company about $8,000 and an $800 co-payment for Amy and her husband.

The assertion that all these sick women are going without treatment is absurd. More prescriptions are written for psychiatric drugs every year in this country than for antibiotics or diabetes medications. On June 30, 2008, CNN Money reported that, for the "sixth year in a row," antidepressants were the number one class of drugs prescribed in the US in 2007. CNN cited a report by the pharmacy benefit manager, Medco Health Solutions, that said 16% of women ages 20-44 take antidepressants.

In 2007, the branded atypical antipsychotics generated $15.9 billion in manufacturer sales in the seven major global markets, with $12.3 billion of those sales in the US, according to an April 2008 report by Sandra Chow on the Decision Resources website.

Thousands of infants harmed

In a September 18, 2008 letter to members of Congress urging them to vote against the Mother's Act, Unite For Life reported that the estimated number of antidepressant-caused infant deaths and injuries over the past four years, based on data from the FDA's MedWatch, were: 4,360 babies born with serious or life-threatening birth defects; 4,160 babies born with potentially fatal heart defects or heart disease; 2,900 spontaneous abortions; and 3,000 premature births.

The so-called experts supporting the Mother's Act constantly minimize the risks. However, a study titled, "Acute Neonatal Effects of Cocaine Exposure During Pregnancy," in the September 2005 Archives of Pediatric and Adolescent Medicine describes adverse effects for cocaine exposed babies eerily similar to those in babies born to mothers taking antidepressants:


"Several central and autonomic nervous system findings, which included hypertonia, jitteriness or tremors, high-pitched cry, difficulty arousing, irritability, excessive suck, and hyperalertness, were noted more frequently on the initial physical examination in the cocaine-exposed cohort. During the hospitalization, the diagnoses of seizures and autonomic instability were more frequently noted in cocaine-exposed infants."
The warnings and precautions section on current labeling for SSRIs and SNRIs contains the following statement:


Neonates exposed "late in the third trimester have developed complications requiring prolonged hospitalization, respiratory support, and tube feeding. ... Reported clinical findings have included respiratory distress, cyanosis, apnea, seizures, temperature instability, feeding difficulty, vomiting, hypoglycemia, hypotonia, hypertonia, hyperreflexia, tremor, jitteriness, irritability, and constant crying. These features are consistent with either a direct toxic effect of SSRIs and SNRIs or, possibly, a drug discontinuation syndrome."
Besides the agony endured by these infants and their families, the additional medical costs are enormous. In 2005, commercial insurers paid an average of $4,247 per day for babies in neonatal intensive care, according to Thomson Healthcare. Direct health care costs for a premature baby average $41,610 or 15 times higher than the $2,830 for a healthy, full-term delivery, a March of Dimes May 2007 report on Preterm Birth estimates.

Advocates of the Mother's Act claim mental illness poses a greater risk to the mother than drug use to fetus. “The problem with this claim is that there is no consideration for the immense stress a mother has to endure when her baby is sick due to this drug use,” says Kate Gillespie, an attorney who handles birth defect litigation at the Los Angeles based Baum, Hedlund, Aristei & Goldman law firm.

“Not to mention the far greater stress that is created by having to constantly deal with life and death health issues, like severe heart defects and respiratory problems, such as persistent pulmonary hypertension of the newborn, caused by SSRI medication," she notes.

Baum Hedlund is currently representing over 200 families whose babies were born with birth defects ranging from congenital heart defects to PPHN after the mothers used SSRIs.


*************
Evelyn Pringle

Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
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Friday, December 05, 2008

Man slashed wrists on Seroxat

It's an old story yet has been brought up again in today's Mail Online. Quite why, I don't know? Unless of course the Coroner is a man of morals and, like many campaigners, knows how dangerous Seroxat can be.

Here's the story.

Man slashed wrists on Seroxat

Safety checks: coroner says more checks need to be carried out

A coroner has called for Britain's biggest-selling antidepressant to be withdrawn after a retired headmaster who was prescribed the drug was found dead with slashed wrists.

Colin Whitfield, 56, died just two weeks after he began taking Seroxat.

At his inquest, Brecon Coroner Geraint Williams said he would be writing to Health Secretary Alan Milburn to demand the drug be withdrawn for further safety checks.

He said: 'I have grave concerns that this is a dangerous drug that should be withdrawn until at least detailed national studies are undertaken.'

'I am profoundly disturbed by the effect this drug had on Colin Whitfield. It is quite clear that Seroxat has a profound effect on the thinking process of anyone who takes it.'

The inquest heard evidence from Mr Whitfield's wife, Kathryn, that her husband of 30 years was a protective and loving father who had been prescribed Seroxat for anxiety.

A fortnight later he locked himself in his garden shed and slit his wrists.

Seroxat - also known as the 'anti shyness pill' - has overtaken Prozac in popularity since it was licensed in 1990. It was prescribed to 400,000 patients in Britain last year.

Some 4,000 users are threatening legal action against makers GlaxoSmithKline saying they suffered unpleasant withdrawal symptoms - including suicidal feelings - after they stopped taking it.

The Government announced a review of Seroxat's safety last year but the drug remains available.

Mr Whitfield, of Llanfrynach, Powys, was prescribed Seroxat last summer.

His widow told the hearing there was nothing to suggest he was suicidal and he had not been suffering from depression.

She said she was certain Seroxat was to blame for his death on August 29.

'It didn't fit the picture of who he was and we have no doubt that it was the drug that caused him to do it,' she said.

'Two days before he died, on his birthday when he was opening presents, he asked, "What more can I ask for than my lovely family?" '

Mrs Whitfield said she was convinced her husband had not been fully conscious of what he was doing.

The Yorkshireman had been looking forward to the coming rugby season and had also written to his mother to say he hoped to see her soon.

'What he did was so totally out of character. He was a very caring, very protective father and husband,' she said. 'He would be hating himself for what he has done to his family.'

The coroner agreed and recorded an open verdict.

'I have a picture of a kindly, gentle, courteous family man whose primary concern was his wife and children,' he said.

'But on this day he didn't care. He did a deliberate act affected, I have no doubt, by the taking of Seroxat.'

Afterwards, Mrs Whitfield said: 'As a result of what the coroner said in court, I really hope something big will come out of this. I hope there will be restrictions on the drug's use because I believe it is very risky.'

Solicitor Mark Harvey, who is representing thousands of claimants, including Mrs Whitfield, in their planned legal action against the drug's makers, said new prescriptions should cease while the drug's safety was examined.

'This case demonstrates our belief that anyone of note who comes across Seroxat expresses concern about what they see,' he added.

GlaxoSmithKline, which manufactures Seroxat, offered its 'sincere condolences' to Mr Whitfield's family but insisted the drug was safe.

It pointed out that those suffering from depression were more likely to commit suicide.'There is no valid scientific research or literature finding that Seroxat causes suicidal thoughts or acts,' it added.

What about the healthy volunteers in the studies Glaxo?









Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

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THE BOSS!

With so much crap going on in the UK at the moment I'm uploading two of my favorite Springsteen videos. 'Twist & Shout' Live and a brilliant version of 'Glory Days' from the Letterman Show. The quality of 'Glory Days' ain't that brilliant... the performance is.

Enjoy







Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
CHIPMUNKA PUBLISHING

AVAILABLE FOR DOWNLOAD HERE


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Thursday, December 04, 2008

THE GREATEST SHOW ON EARTH!




Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

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CHIPMUNKA PUBLISHING

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Tuesday, December 02, 2008

Dr Martin Scurr - Daily Mail - Dumbass Award.

There are some doctors who just haven't got a clue when it comes to handing out advice regarding Seroxat, some of these doctors are in the public eye [TV, Newspaper columns etc]. One such doctor is Dr Martin Scurr who writes a Q&A section in the Daily Mail.

Scurr was recently contacted by an 83 year old depressive whom was enquiring about a lightbox or sunshine lamp for seasonal affective disorder [S.A.D.]

Scurr's response is jaw dropping. You can view it here. Meantime, I have selected his thoughts [advice] on Seroxat.

"You're already taking a good anti-depressant medicine and I am sorry you do not feel happier."

"You cannot conclude that Seroxat has failed until you've been taking the full prescribed dose for at least six weeks. Some would argue that the level should be as high as 60mg and you should discuss your current prescription with your doctor."


What I find difficult to believe is Scurr's failing to really delve into the heart of the question from this 83 year old woman. Part of her question was, " I am 83, a depressive and take Seroxat tablets (30mg once daily) but still don't feel all that happy." Now, wouldn't it have been better if Scurr had asked her a series of questions before advising her?

May I remind Doctor Scurr that the daily recommended dose of Seroxat is 20 mg! and point him toward the MHRA website, "A review of clinical trial data on the use of paroxetine (Seroxat) in adults has confirmed that, as stated in the summary of product characteristics, 20 mg is the recommended daily dose in adults." Not only that, the MHRA also go on to say that, "There is no evidence from clinical trials that increasing the dose above the recommended dose increases efficacy", and yet here we have a doctor handing out advice that is the complete opposite to what the regulator recommends!

This really grinds my teeth. The whole crux of my meeting with the MHRA back in September was to highlight the lack of education that many doctors have when it comes to prescribing Seroxat and other SSRi's, also a lack of understanding when it comes to spotting withdrawal as opposed to the disease [Depression etc]. This shoddy advice is a classic example of the the point I was trying to make. Dr Scurr is not only wrong here, he is DANGEROUSLY wrong and for that I hereby award him the Seroxat Sufferers Dumbass Award.

Dr Scurr you are a dumbass!

Fid



Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
CHIPMUNKA PUBLISHING

AVAILABLE FOR DOWNLOAD HERE


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Monday, December 01, 2008

SSHHHHHERVARIX

GSK fly in experts to persuade government to reverse decision.






"GSK is sponsoring the visit to Ireland on Friday of Dr Anne Szarewski, another cervical cancer expert, who is clinical consultant at the Wolfson Institute of Preventive Medicine in the UK. Szarewski will also be speaking to Irish consultants, healthcare professionals and stakeholders about the importance of the vaccine."



MULTINATIONAL drug companies are pressing the government to introduce a cervical cancer vaccination programme by flying experts to Ireland to talk to consultants.

At least one of the companies, GlaxoSmithKline (GSK), hopes to meet Mary Harney, the health minister, to try to convince her to put a vaccine contract for the programme out to tender.

GSK claims Harney cannot estimate the cost of the scheme until after a competitive bidding process, and predicts that the price will be much lower than the €14m quoted by the health department.

Last week, Sanofi Pasteur MSD, which produces the cervical cancer vaccine Gardasil, sponsored a trip to Ireland by Professor Margaret Stanley of Cambridge University, an expert on cervical cancer. Stanley was in Dublin on Thursday to speak to a group of consultants and public healthcare professionals about the benefits of the vaccine.

FULL STORY HERE



Well GSK are really pushing this baby ain't they? If they ain't promoting it via kiddies websites such as Lola's Land, they are 'bigging it up' with claims that it is a cure for cervical cancer!



According to the New England Journal of Medicine it is being widely used without sufficient evidence about whether it is worth the high cost or even whether it will effectively stop women from getting the disease.



I've stated before on this blog that it is a tough decision for any parent to make. The promotion obviously will sway any decision. Remember how they kept tight lipped when Paxil was being prescribed in the States for kids, they even kept quiet when it was being prescribed for kids here in the UK, albeit off-label - basically, 'off-label' means, we [GSK] can put the blame on the doctor if anything goes wrong.



Here's some other instances where it went wrong for GSK and its vaccines:



Body Count Linked to GSK Vaccine Trial Rises

UK babies given toxic vaccines, admits Glaxo

Drug Company Admits Unsafe Vaccines Were Used

The Bitter Feud over LYMErix

New York's HIV experiment



*Earlier this month news broke that rat poison is being used in the HPV Vaccine in America



Hat Tip - The Truthman


Read the new book, The Evidence, However, Is Clear...The Seroxat Scandal

By Bob Fiddaman

ISBN: 978-1-84991-120-7
CHIPMUNKA PUBLISHING

AVAILABLE FOR DOWNLOAD HERE


PAPERBACK COMING SOON


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