Zantac Lawsuit


Researching drug company and regulatory malfeasance for over 16 years
Humanist, humorist
Showing posts with label Defective Drug. Show all posts
Showing posts with label Defective Drug. Show all posts

Thursday, June 16, 2011

Dear GlaxoSmithKline, Have I Got News For You

Image: ngpharma.eu.com


I have an exclusive coming to this blog soon regarding GlaxoSmithKline's patient aftercare, or lack of it.

Regular readers or those that have had dealings with Britain's largest pharmaceutical company won't be surprised at Glaxo's lack of care and its shirking of responsibility to its consumers - its shareholders might though.

It appears to me that they [GSK] do not only try to intimidate experts who speak out against their products or bloggers who upload videos to youtube, they also try to intimidate someone who asks them for help regarding withdrawing from one of their drugs - I mean, what other company do you know would get a lawyer to phone up someone who had requested help in tapering off Seroxat?



Coming very soon to this blog.

Glaxo and/or the lawyer in question may leave a comment once the story is up and running.

Fid


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'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
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Tuesday, June 02, 2009

Antidepressants linked to recurrent breast cancer

I hate to be the one to tell Nursing Times that this was known back in 2000, nine years ago!

Research done by Michelle Cotterchio, M.D., of Cancer Care Ontario found that women who took Paxil saw their risk of breast cancer increase by seven times even when other possible risk factors were fully accounted for. (Citation: New England Journal of Medicine, Vol. 342, June 29, 2000, p. 2003.)



Source: Nursing Times

1st June 2009


Research shows antidepressants can increase the risk of recurrent breast cancer while taking the cancer prevention drug tamoxifen.


According to a new study by Medco Health Solutions, drugs prescribed for depression including fluoxetine, paroxetine and to a lesser extent sertaline can virtually wipe out the benefit tamoxifen provides.

Tamoxifen cuts the chances of breast cancer recurrence by half, but many patients take antidepressants for hot flashes as an alternative to hormone pills which are not considered safe after breast cancer.

It has long been thought that some antidepressants can lower the amount of tamoxifen’s active form in the bloodstream, but this study, which is the largest to look at the issue, confirms the drugs` interfering nature.

Scientists looked at 353 women taking tamoxifen plus other drugs that might interfere with it and 945 women taking tamoxifen alone.

The women were tested for second cancers in the following two years and the findings show breast cancer recurred in 7% of women on tamoxifen alone, but by 14% in women taking other drugs that could interfere.

The antidepressants paroxetine and fluoxetine were the most likely to increase the risk of recurrent breast cancer.

----

Fid

ORDER THE PAPERBACK
'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
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Tuesday, May 19, 2009

MD Calls for immediate embargo of all antipsychotics and antidepressants

Newswire

Fred A. Baughman Jr., MD Announces: Vets' Sudden Cardiac Deaths Are Not Suicides or Overdoses

EL CAJON, Calif., May 19 /PRNewswire/ -- Fred A. Baughman Jr., MD today announced the results of his research into the "series" of veterans' deaths acknowledged by the Surgeon General of the Army.


Upon reading the May 24, 2008, Charleston (WV) Gazette article "Vets taking Post Traumatic Stress Disorder drugs die in sleep," Baughman began to investigate why these reported deaths were "different." And, why they were likely, the "tip of an iceberg."


Andrew White, Eric Layne, Nicholas Endicott and Derek Johnson were four West Virginia veterans who died in their sleep in early 2008. Baughman's research suggests that they did not commit suicide and did not overdose as suggested by the military. All were diagnosed with PTSD. All seemed "normal" when they went to bed. And, all were on Klonopin (a benzodiazepine), Paxil (an SSRI antidepressant) and Seroquel (an antipsychotic).


On January 15, 2009, the New England Journal of Medicine (Ray et al), reported that antipsychotics double the risk of sudden cardiac death.


On February 7, 2008, Surgeon General Eric B. Schoomaker, said there has been "a series of deaths in Warrior Training Units" -- "often as a consequence of the use of multiple prescription and nonprescription medicines and alcohol ... we all saw the unfortunate death of Heath Ledger, the 'Brokeback Mountain' star, who died from an accidental overdose."


But Ledger was not on any heart-toxic medication. When found, his pulse and respirations were intact! When found, none of the veterans were breathing or had pulse. There's, most likely, were sudden cardiac deaths!


Sudden cardiac death is an unexpected death due to cardiac causes occurring in a short time period (generally within 1 h of symptom onset) in a person with known or unknown cardiac disease in whom no previously diagnosed fatal condition is apparent. (Medscape e-Medicine 7/17/06)


As of April 16, 2009, veteran's wife, Diane Vande Burgt, had Googled 19 "dead in bed," 36 "dead in barracks," or "... room," and 19 "under investigation." Removing reported "suicides" shortened our original list by 15 names leaving a total of 74 probable sudden cardiac deaths - most in soldiers or veterans in their 20's. An article from the AP, San Antonio, 4/17/09, reported "The deaths of two soldiers are being investigated ... both men apparently died in their sleep."


It was reported in June, 2008, that 89% of veterans with PTSD are given antidepressants and 34% antipsychotics (Mohamed & Rosenheck, June 2008). A third, then, are exposed to the additive potential of both to cause sudden cardiac death. (Sicouri & Antzelevitch, 2008)


On April 13, 2009, Baughman wrote the Office of the Surgeon General of the Army: "the Surgeon General said there has been 'a series, a sequence of deaths' Has the study of these deaths been published?


On April 17, 2009, the response came: "The assessment is still pending and has not been released yet."


There being no such thing as an essential psychiatric drug, I call upon the military for an immediate embargo of all antipsychotics and antidepressants until there has been a complete, wholly public, clarification of the extent and causes of this epidemic of probable sudden cardiac deaths.

ORDER THE PAPERBACK
'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
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Wednesday, May 13, 2009

Paxil [Seroxat] “defective and unreasonably dangerous product.”

Source: SSRi Stories

One day after his antidepressant medication was doubled, a Whitfield County man threw himself in front of a moving train, killing him.

Now, his widow is suing the drug manufacturer claiming the medication, Paxil, was to blame, and she is looking to be compensated the “full value” of her husband’s life and for the drug to carry severe warnings.

The widow, Donna Dietz, is suing the Smithkline Beecham Corporation, the makers of the drug she contends led to the death of her 33-year-old husband, and has enlisted the help of a Houston-based firm that specializes in these cases. Click here to view a copy of the lawsuit.

At the time of his death in 2002, according to a lawsuit filed in U.S. District Court in Rome, Garrison David Dietz had been prescribed the drug Paroxetine, branded as Paxil, by his doctor.

In the lawsuit, Dietz, who now lives in Gordon County, states a judgment of more than $75,000 is the goal of the suit.

Attorney Andy Vickery, who represents Dietz, said the amount would be a great deal more, saying a similar four-party suit in Wyoming in 2001 earned his clients $8 million in compensation.

One week after beginning the medication, the doctor doubled the dosage; one day later, April 10, 2002, Dietz’s husband committed suicide, the suit says.

The suit describes Paxil as a “defective and unreasonably dangerous product.”

Vickery said his goal is to strictly limit the prescription of this and similar drugs, selective serotonin reuptake inhibitors (SSRI), to that of psychiatrists.

Attorney’s for Smithkline Beecham could not be reached for comment Tuesday

----

Fid

ORDER THE PAPERBACK
'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
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Monday, May 11, 2009

COMING SOON

Why I think paroxetine is a defective drug and why I think GlaxoSmithKline are running scared.

If correct, this will blow your socks off folks.

Keep watching.


Fid


SEROXAT SUFFERERS STAND UP AND BE COUNTED

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'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
SIGNED COPIES HERE OR UNSIGNED FROM CHIPMUNKA PUBLISHING

Saturday, May 09, 2009

GSK - Prescription Drugs and Other Products

Paxil/Seroxat/Aropax [1]

Manufactured, marketed, dispensed, despite GSK knowing that it could make people taking it suicidal.

Imitrex/Sumatriptan [2]

At least 43 deaths and 139 "life threatening" reactions have been linked through MedWatch reports to Imitrex [sumatriptan], a migraine drug introduced by Glaxo subsidiary Cerenex Pharmaceuticals as Imitrex after FDA approval at the end of December 1992. Reports began in 1993, less than a year after Imitrex went on the market. The company sent out "Dear Doctor" letters highlighting "drug-associated fatalities" last August. The revised label describes the death of a 41-year-old woman.

Avandia [3]

GlaxoSmithKline’s popular drug for treating type 2 diabetes, increased the risk of heart death by 64% and the risk of heart attack by 43%.


Advair [4]

The FDA says GSK's Advair and other long-acting beta 2 agonists have been associated with increased risk of severe asthma exacerbations and asthma-related death, and should carry warnings about the serious side-effects.

Lotronex [5]

FDA reviewers found that Lotronex improved symptoms in only 10% to 20% of the patients. Still, an FDA advisory committee, whose participants included a paid consultant to Glaxo, unanimously recommended approval. (The yes vote voiced by the Glaxo consultant, Dr. Arnold Wald of Pittsburgh, was invalid, agency officials say, because of his status as a temporary appointee.)

Lymerix [6]

Alleged that SmithKline violated state negligence and consumer laws by not warning of potential dangers. And they complain that Yale University may have had a conflict of interest in testing the vaccine because it stood to earn royalty payments from LYMErix sales.

Relenza [7]

Since 1999, when Relenza was approved, there have been 115 reports of psychiatric events, of which 74 were children.

Alli [8]

At 240 pounds, she thought Alli might do what dieting alone had not. On Alli, she lost ten pounds right away. Then her weight loss slowed, and the side effects began. They were so serious she ended up in the emergency room twice. "I couldn't control my bowels. I was running to the bathroom, leaving meetings, being in the car, and literally stuck," she recalled.

Cervarix [9]

A GROUP of British teenagers has launched the first legal action against the makers of a controversial ­cervical cancer jab. They have suffered symptoms ranging from paralysis and ­seizures to fatigue and muscle aches since being given the Cervarix vaccine.

Ribena [10]

Two 14-year-old New Zealand girls made the news recently when their school science project revealed that Ribena, the popular black currant drink, did not have the high levels of vitamin C it claimed to.

AZT [11] AND [12]

Orphans and babies as young as three months old have been used as guinea pigs in potentially dangerous medical experiments sponsored by pharmaceutical companies, an Observer investigation has revealed.

British drug giant GlaxoSmithKline is embroiled in the scandal. The firm sponsored experiments on the children from Incarnation Children's Centre, a New York care home that specialises in treating HIV sufferers and is run by Catholic charities.

[12]

President Mbeki's directive on 28 October 1999 that the safety of AZT be investigated on the basis that "there is a large volume of scientific evidence...that [AZT] is harmful to health" alerted the South African public to the fact that AZT is dangerously poisonous.

----

Combine the above with hidden studies, faked studies, ghost written studies, and huge sums of money paid to 'Key Opinion Leaders' and you have one hell of a psychopathic killer on your hands.

Fid




[1] Trail of Paxil Suicides Leads To GlaxoSmithKline
[2] What you--and maybe your doctor--don't know about your prescription's side effects could hurt you. Or even kill you
[3] 'Glaxo's diabetes drug Avandia raises heart-death risk'
[4]
Asthma drug warning hits GlaxoSmithKline
[5]
"Irritable bowel" remedy pulled after reports of serious injuries.
[6]
SmithKline Beecham Faces Lawsuit for Lyme-Disease Vaccine's Negative Effects.
[7]
Relenza Should Have Psychiatric Side Effects Warning, Say Regulators
[8]
Alli - Wonder Drug or Rip-Off?
[9]
Teenage Girls Sue over Cervarix Cancer Jab
[10]
Ribena ri-busted
[11] GlaxoSmithKline embroiled in scandal in which babies and children were allegedly used as 'laboratory animals'
[12] OPEN LETTER TO GLAXO-SMITH-KLINE


GlaxoSmithKline:

"We have a challenging and inspiring mission: to improve the quality of human life by enabling people to do more, feel better and live longer."


SEROXAT SUFFERERS STAND UP AND BE COUNTED

ORDER THE PAPERBACK
'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
SIGNED COPIES HERE OR UNSIGNED FROM CHIPMUNKA PUBLISHING

Monday, May 04, 2009

Ruling reopens drug lawsuits

Source: New Jersey Business News

TWO BIG CASES

Three days after ruling on Wyeth, the Supreme Court sent two suits over antidepressants back to the federal appeals court in Philadelphia, which had rejected them on preemption grounds.

The cases, both on alleged failure to warn of the risk of suicide, include one against Glaxo over Paxil and one against New York-based Pfizer over Zoloft. Pfizer has a strong presence in New Jersey, employing about 1,600 people at operations in Peapack-Gladstone, Bridgewater and Morris Plains.

GlaxoSmithKline was to go to trial May 4 in Philadelphia on claims by the family of Thomas Turek, who killed himself on his 47th birthday in 2003, eight days after he started taking Paxil.

The antidepressant made him agitated and paranoid, and the company understated its side effects, his family said.

The judge refused to throw out the case, citing the Wyeth decision. Glaxo settled the case April 24 on confidential terms.

Sarah Alspach, a Glaxo spokeswoman, confirmed the settlement and declined to comment further.

The court's decision on the Turek case will be extended to about 25 other Paxil suits in Philadelphia, the patients' lawyer, Bijan Esfandiari, said. The first trial will be July 20.

Glaxo, based in London, also settled a Paxil case set for trial Monday in Cheyenne, Wyo., after the court rejected the pre-emption argument because of the Wyeth decision. The family of Jack Van Dyke sued in 2005, claiming Paxil was responsible for his suicide. Settlement terms weren't disclosed.


FULL STORY

Fid

ORDER THE PAPERBACK
'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
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Breastfeeding - SSRi's are safe - Advice given to Physician Assistants

Breastfeeding and have Post-Partum depression?

Take an SSRi

That's the advice given on the 'Advice For Physician Assistants' website.

In fact, they go as far to say:

"New mothers who develop postpartum depression and who want to breastfeed their infants present a treatment challenge. SSRIs may be a safe and effective option for mother and child alike."

Not only that, they further advise:

"Selective serotonin-reuptake inhibitors (SSRIs) are the first medication treatment choice for PPD due to their ease of administration, low toxicity and greater tolerability.This class of antidepressant is the most studied in mother-infant pairs."

Here is what they say about two SSRi's:

Fluoxetine:
The most studied SSRI regarding use in pregnancy and breastfeeding. Compared with paroxetine and sertraline, fluoxetine produces the highest concentration of medication in breastfed infants at levels above 10% of the maternal dose, but fluoxetine levels in breast milk typically were low (less than 5 ng/mL) with maternal dosage of 20 mg per day or less.

Sertraline (Zoloft)
Based on multiple case series, sertraline has been recommended as the first-line treatment for breastfeeding mothers.

Dig deeper and research exactly who funded these studies.

Fid



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'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
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Sunday, May 03, 2009

Look back at Panorama

This great article by Charles Medawar was posted a day after BBC TV aired their 4th, count them, 4th programme about GlaxoSmithKline's Seroxat.

It's well worth a read.


"What they’ve done is just despicable … "

Panorama (BBC-TV) last night broadcast its fourth programme on Seroxat® (paroxetine), a still deeper foray into the built-in nastiness of drug marketing and product promotion. All credit to the programme for sticking with the issue, if only to reveal how much more must be done to see this story through.

Thanks largely to Panorama and friends we now have a pretty clear picture of motive, opportunity, method and the sometimes awful consequences. Corrupting influence in pharmaceutical science has become almost natural and easy - the product not only of greed and self-interest, but of established professional and organisational practice. In some ways, collective lack of commitment and imagination seem to trump venality. Indifference rules, OK?
The more this story unfolds, the more scary seems the inter-dependence and over-connectedness of the three main powers. Between them, the Pharmas and their agents, governments and regulators, and doctors and research workers have constructed a ‘health-care’ system that now seems, almost routinely, to put health second and them on top.

Panorama of course illustrated the point in vivid microcosm and partly by reference to villains, heroes and victims. This was allegory, like John Le CarrĂ©’s The Constant Gardener: how else does one encapsulate the wider point and bring it home? Only in human scale, with familiar dimensions, does full meaning begin to come clear. Statistics may point to part of the reality, but they don’t bleed.

Now, in close-up, we see silky but sweaty denials from once trusted experts; they reveal not only grand arrogance, but also the crippling impact of institutional imperatives and their seductive, crushing effect on decent personal values. The human anguish that follows tops the iceberg that threatens to sink us all. The sickness feels palpable: what is happening to humanity, honest science and real health?

These words, "What they’ve done is just despicable", were spoken by the mother of a 16-year old girl, when she later came to understand the cause of her loss. She had returned home to find her daughter hanging from the upstairs loft hatch; her body was still warm, but beyond revival. A packet of Seroxat tablets was next to the suicide note. That was in 2003, less than a month before the UK regulators published warnings about this drug – don’t give it to under 18-year olds. This was on the basis of evidence from clinical trials that the manufacturers had held for several years.

In these circumstances, the word, ‘despicable’ seemed moderate. The case for meticulous investigation seems all the more compelling, when the victims include an eleven year old on paroxetine, who had used his puppy’s leash to hang himself in a closet in the family home. There are too many tragic cases to mention: Christopher Pittman is another. He was prescribed paroxetine, then sertraline, and is now in the early stages of a 30 year prison sentence; he shot his grandparents aged 12 years old.

The focus in this programme was on Study 329, the centrepiece of a small series of clinical trials to investigate the effects of paroxetine on depressed adolescents and children. The scientific evidence available to SmithKline Beecham in 1998 suggested both lack of effectiveness and a possible excess risk of drug-induced self-harm.

The company held back the evidence, until the UK regulators chanced on it, in May 2003. They issued warnings soon after, estimating that the risk of drug-induced suicidality was three times greater with paroxetine than with no drug treatment (placebo). Later, the US Food & Drug Administration required a proper re-examination of the raw data: this established (2006), that the risk of suicidality, on-drug, was actually six times greater for children (three times greater for adults) than originally assumed.

Initially, the company decided not to publish the results of Study 329: memoranda now in the public domain record advice that it would be "commercially unacceptable" to disclose the facts, because it "would undermine the profile of paroxetine". Instead, the decision was "to effectively manage the dissemination of these data". This was so well managed that even sales representatives were led to believe that the drug "demonstrates remarkable efficacy and safety in treating the adolescent population". Sales (detail) people thus become potentially dangerous (if willing) victims, like the doctors who too willingly take their advice.

At this point in the programme, Shelley Jofre, the Panorama reporter, asked US attorney, Karen Barth Menzies what she made of that claim: "remarkable safety and efficacy". It was a lie, and fraud, she replied. The question seemed almost redundant, not just because of the weight of the evidence – but also because both of them have been chasing the truth on these issues for years. They are among the heroes, along with the brave, indefatigable Professor David Healy. He is the shining exception to the general rule, that these accusations have come from outside the establishment, not within.

How was all this achieved? It was of course the product of a complex collective effort, but Panorama could fairly point the finger at some especially conspicuous players. Two were influential and hitherto well-respected US academic psychiatrists, Drs Martin Keller and Neal Ryan. Both earned and gained very handsomely by touting the product and fronting for the manufacturers, (now GlaxoSmithKline, GSK). They too casually lent their names to misleading, fine-woven conclusions in prestigious publications, the product of assiduous ghost-writing and marketing steer.

Also conspicuous was the scarily brazen editor of a leading US psychiatric journal, Child and Adolescent Psychiatry. She emphasised she had "no regrets at all" about publishing the invisibly concocted and misleading version of Study 329, on the grounds that, "it generated all sorts of useful discussion".

Then there is Dr. Alastair Benbow, the Head of European Clinical Psychiatry at GlaxoSmithKline, who featured so prominently in two earlier Panorama programmes. Five years after the company’s own evidence revealed no such thing, Benbow insisted that there was nothing to worry about. "The reality of the situation is that, in this trial (Study 329), Seroxat was generally well tolerated by this difficult to treat population," he claimed.

Meanwhile, GlaxoSmithKline has issued a bullish statement to Panorama: "In developing Seroxat, GSK has always been strongly conscious of the duty it owes to the millions of patients who suffer from depression and refutes any allegation that it has failed in this duty. GSK utterly rejects any suggestion that it has improperly withheld drug trial information …" The statement does not specifically address Panorama's concerns; the full text can be read here.

So what is to be done? The short answer is almost everything, given that the so-called competent authorities have repeatedly failed to put their house in order. Previous episodes of Panorama have documented the grovelling impotence of the drug regulators (notably the MHRA and the FDA) and the passive connivance of the medical profession – of course with countless individual exceptions (no doubt including your doctor as well as mine).

Where do we go from here? In the immediate future, there is potential for progress on three main fronts – none politically attractive, though central to the future health and reputation of pharmaceutical medicine.

First, we need urgently to examine the meaning of personal responsibility in corporate settings: specifically, the General Medical Council (GMC) should now investigate and rule on the conduct of Dr Alastair Benbow. Both would in some way be on trial. The GMC is a professional court with feudal if honourable traditions, with still some way to catch up with the climate of the late 20th century. As for Dr. Benbow, he seemed so sincere in his advocacy for the drug, so replete with reassurance, that his position must now be clarified. Did he critically review the relevant scientific evidence before making these claims? Was he a leader in some cynical process, or kept well ignorant and brilliantly coached in his denials? The latter seems much more probable, but we need to know for sure. Are these horrible and damaging drug disasters driven by knaves, fools, or victims - or some, none or all of the above? The GMC must now rise to the occasion: we need some definitive view.

Secondly, what of the proposed prosecution of GlaxoSmithKline by the UK authorities (led by the Medicines and Healthcare products Regulatory Agency)? In the USA, civil actions will progress later this year, seeking to link the now damning factual evidence with tragic human consequences. But in Britain, are we now due for a replay of Prime Minister Blair’s recent decision to abort the bribery investigation into British Aerospace (BAE), on the grounds of national interest and security? What is the MHRA up to? Their last word (7 April 2006) was this – but what’s new?

"The conduct of the investigation required the Enforcement Division of the MHRA to consider over a million pages of scientific and other documentation which comprised the factual background to the case. A team of medics and scientists from across the MHRA assisted with this. The process of considering documents is now completed and documents are only reviewed now if they come to light as new evidence. Potential witnesses from inside the MHRA have been interviewed and notes have been taken from them, from which statements will be drafted. These statements seek to convert the findings of the review of the scientific and regulatory documentation in to evidence suitable for the conduct of a criminal trial, if appropriate … Once the criminal investigation has been concluded a file will be forwarded to prosecuting lawyers within the legal department of the Department of Health. They will apply the Code for Crown Prosecutors to decide whether or not there will be a prosecution."

Thirdly, we urgently need some proper enquiry into the conduct and effectiveness of the UK drug regulators themselves - the Medicines and Healthcare products Regulatory Agency (MHRA) - in line with the 2005 recommendations of the Parliamentary Health Committee, in its report on ‘The Influence of the Pharmaceutical Industry’. The evidence from this and earlier Panorama programmes hugely underlines the importance of this main recommendation:
"During this long inquiry we became aware of serious weaknesses in the MHRA. Worryingly, in both its written and oral evidence the Agency seemed oblivious to the critical views of outsiders and unable to accept that it had any obvious shortcomings, except those that could be remedied by more transparency. The Agency’s attitude to its public health responsibilities suggested some complacency and a lack of requisite competency, reducing our confidence in its ability to undertake the reforms needed to earn and deserve public trust. Nor did we conclude that the MHRA provides the discipline and leadership that this powerful industry needs. We recommend that there be an independent review of the MHRA …"

This may seem a tall order, but so much seems badly wrong. This Panorama programme was a potent reminder of that – an emphatic, evidence-based and well-focused scream for medicines that honestly do work.

Declaration of interest: I have a critical, passionate and long-standing interest in the SSRI antidepressant story: see Medicines out of Control? I played no part in the making of this Panorama, but undertook (with Dr Andrew Herxheimer) an analysis of viewers’ emails for the second programme in the series, for which I was paid about £1,350. I was also engaged (2004/5) as a specialist adviser on the Parliamentary Health Committee enquiry into The Influence of the Pharmaceutical Industry.

Charles Medawar
30 January 2007

Read more of Charles Medawar's brilliant website, Social Audit, HERE

____

Fid




Related links:

Seroxat update 14 Sep 06 Panorama

Secrets of the drugs trials: Transcript 31 Jan 07 Panorama

Taken on trust 21 Sep 04 Panorama

Seroxat: Emails from the edge 28 Apr 03 Panorama

The secrets of seroxat 10 Oct 02 Panorama


SEROXAT SUFFERERS STAND UP AND BE COUNTED

ORDER THE PAPERBACK
'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
SIGNED COPIES HERE OR UNSIGNED FROM CHIPMUNKA PUBLISHING

Saturday, May 02, 2009

720% Increased Risk Of Breast Cancer From Paxil

Cancer Risks Associated With Paxil Usage

The American Journal of Epidemiology published two studies in 2000 by Cotterchio and colleagues which demonstrated that Paxil presented a 720% increase in risk of breast cancer in females.

The Canadian Cancer Society website indicates that for heavy smokers there is a 400% increase in risk for cancer. In other words, Paxil use presents a greater risk factor for breast cancer then smoking. With over 3,000,000 Canadian prescriptions for Paxil in the year 2000 this is major cause for concern.

Source: rense.com

Hat tip: The Truthman

Fid


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'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
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Friday, May 01, 2009

Are SSRi's Behind Iraq Soldier Suicides?



Source: The Epoch Times

Are VA Protocols Behind Iraq Soldier Suicides?
By Martha Rosenberg

Why are suicides among Iraq war soldiers twice that of other wars?

One reason could be that 80 percent of troops with post-traumatic stress disorder (PTSD) are given drugs that didn’t exist during other wars.

Antidepressants like Prozac, Zoloft, Paxil, Celexa (selective serotonin reuptake inhibitors or SSRIs), Cymbalta, and Effexor (serotonin norepinephrine reuptake inhibitors or SRNIs) are so closely associated with suicide that they carry suicide warnings.

According to published newspaper reports, 660 people, including at least 17 Iraq war veterans, have killed themselves on SSRIs and SNRIs since 1988. Many more have attempted suicide and committed felonies, self-harm, police stand-offs, murders, murder/suicides, and mass murders with high-powered weapons.

Yet what does the U.S. Department of Veterans Affairs suggest as a treatment for PTSD?

“We recommend SSRIs as first-line medications for PTSD pharmacotherapy in men and women with military-related PTSD,” says the VA’s National Center for PSTD’s Iraq War Clinician Guide, 2nd Edition. “Findings from subsequent large-scale trials with paroxetine [Paxil] have demonstrated that SSRI treatment is clearly effective both for men in general and for combat veterans suffering with PTSD.” {what?}

In fact, 89 percent of veterans with PTSD are given antidepressants, and 34 percent are given antipsychotics, according to an article in the June 2008 Journal of Clinical Psychiatry.

In April, Dr. Fred Baughman and family survivors presented the deaths of two veterans who were taking the leading antipsychotic, Seroquel, to an FDA committee that is considering widening the drug’s use.

A January 2009 Journal of Affective Disorders article by VA authors recommends “close monitoring” for suicide for 12 weeks “following antidepressant starts,” when risk greatly rises. While scientific studies continue to confirm the danger of SSRI use in young and bipolar patients, another voice says it’s not what it looks like.

“Suicide attempt rates were lower among patients who were treated with antidepressants than among those who were not,” says an article in the July 2007 American Journal of Psychiatry (“Relationship Between Antidepressants and Suicide Attempts: An Analysis of the Veterans Health Administration Data Sets”) by Robert Gibbons, director of the Center for Health Statistics at the University of Illinois at Chicago. “These findings suggest that SSRI treatment has a protective effect in all adult age groups. They do not support the hypothesis that SSRI treatment places patients at greater risk of suicide.”

This is not the only time Gibbons has gone to bat for the controversial antidepressants.

In an article called “Early Evidence on the Effects of Regulators’ Suicidality Warnings on SSRI Prescriptions and Suicide in Children and Adolescents” in the September 2007 American Journal of Psychiatry, he indicated “black box” suicide warnings that the FDA mandated in 2004 for a national rise in young peoples’ suicides. Why? Because the warnings discouraged doctors from prescribing SSRIs!

Of course the “SSRI deficiency” argument is as insipid as blaming the obesity epidemic on the unavailability of fen-phen. But many joined Gibbons in the round of big pharma “I-told-you-sos,” including Charles Nemeroff of Emory University School of Medicine, who was later disgraced for undisclosed pharma conflict of interests.

Unfortunately, Gibbons was wrong. The suicide stats he analyzed did not yet reflect the effect of the black box warnings and he ended up having to tell The New York Times the “early evidence” was actually not evidence at all, but “suggestive.”

Worse, Zoloft-maker Pfizer contributed $30,000 to the article’s belly flop, writes Alison Bass, author of “Side Effects: A Best-Selling Drug on Trial,” in the Boston Globe. Not much return on investment there.

Of course it should come as no surprise—except to journal editors—that Gibbons is financially linked to Effexor-maker Wyeth, now Pfizer, and that his second author, John Mann, is linked to Pfizer and GlaxoSmithKline.

A bigger surprise is that Gibbons is rolling in taxpayer-funded grants from the National Institute of Mental Health, including some to study antidepressants and suicide.

What firewalls are in place to keep pharma “science” from becoming government science, promoting deadly pills?

What protects U.S. taxpayers, public health monies, and, most importantly, our veterans?

Martha Rosenberg is a freelance writer.

May 01, 2009

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Fid


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Dear Doctor... I'd like to show you something...

For those struggling with Seroxat/Paxil, you are probably faced with ignorance of doctor's and healthcare professionals as you describe your withdrawal problem to them. GSK Reps would have told them that the withdrawal lasts only maybe 2 weeks or so.

If you are frustrated that your Doc won't take you seriously or he drops your dose so drastically that you seem to be going out of your head with electrifying zaps [Known in the trade as 'dizziness'] - then print off the following and present it to your doctor.

A tapering protocol for all SSRi's may be available soon, it will only be a guide, but a guide is what is needed rather than the usual 'The patient must taper slowly' line that appears on patient information leaflets.

This from ehealthme.com regarding side effects and effectiveness of Seroxat/Paxil/Aropax (paroxetine hydrochloride) for females and males at all ages.

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On Apr, 9, 2009: 62,164 related incidents are studied



**Notice the reductions in adverse reactions from 2004 onwards? This, I beleive, is a result of the public awareness created about Paxil/Seroxat both here in the UK and in America.

Overall results of Paxil:
Top drug interactions, adverse side effects of Paxil:



Bring a copy of this report to your health teams to ensure drug risks and benefits are fully discussed and understood.

For other SSRi's visit http://www.ehealthme.com/

Fid

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Thursday, April 30, 2009

GlaxoSmithKline settle 2 Paxil cases 'Out of Court'

These two slipped under the radar, proof that settlements made out of court rarely make the news when settled at an early stage.

This from Bloomberg, April 30th 2009

GlaxoSmithKline was to go to trial May 4 in Philadelphia on claims by the family of Thomas Turek, who killed himself on his 47th birthday in 2003, eight days after he started taking Paxil.

Side Effects

The antidepressant made him agitated and paranoid, and the company understated its side effects, his family said.

The judge refused to throw out the case, citing the Wyeth decision. Glaxo settled April 24 on confidential terms.

Sarah Alspach, a Glaxo spokeswoman, confirmed the settlement and declined to comment further.

The court’s decision on the Turek case will be extended to about 25 other Paxil suits in Philadelphia, the patients’ lawyer Bijan Esfandiari said. The first trial will be July 20.

Glaxo, based in London, also settled a Paxil case set for trial May 4 in Cheyenne, Wyoming, after the court rejected the preemption argument because of the Wyeth decision. The family of Jack Van Dyke sued in 2005, claiming Paxil was responsible for his suicide. Settlement terms weren’t disclosed.

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Fid

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Monday, April 27, 2009

Hamilton Depression Scale and GSK






According to Wikipedia The Hamilton Rating Scale for Depression (HRSD), also known as the Hamilton Depression Rating Scale (HDRS) or HAM-D, is a 21-question multiple choice questionnaire that clinicians may use to rate the severity of a patient's major depression. Max Hamilton originally published the scale in 1960 and reviewed and evaluated it in 1966,1967,1969 and 1980.

A paper released in 2008, that a reader kindly sent me, entitled, 'Sensitivity of the individual items of the Hamilton depression rating scale to response and its consequences for the assessment of efficacy', begs to differ.

The conclusion of the paper:

In conclusion, this study adds further data to the body of evidence that HAM-D17 is not the most sensitive measure of treatment effect in depression trials. This is especially important in early clinical development studies, in which relatively small patient populations are included, increasing the risk of false negative results. The social and financial costs of false negative results are not acceptable in an indication which urges for medicines with a better efficacy profile.

Furthermore, we show that a considerable reduction in population size can be achieved when the subscales are used due to an increase in statistical power to detect differences from placebo. Such a smaller group size does not only reduce the run time of a study, it is also limits the unnecessary exposure of patients to placebo treatment. From the two subscales we have devised, subscale 1, derived from graphical analysis of the longitudinal patterns of individual items, performs better in the detection of treatment effect than subscale 2. Therefore,we recommend the use of this response-based HAM-D7 subscale as primary endpoint for the statistical analysis of efficacy data rather than the HAM-D17.


As with all papers, a conflict of interest declaration was made:

There are no arrangements of financial nature, or of any other kind, that could lead to conflict of interests with regard to this manuscript.

One look at two of the three co-authors of this paper would suggest otherwise.

Meindert Danhof works at the Clinical Pharmacology and Discovery Medicine, GlaxoSmithKline, Verona, Italy

and

Oscar Della Pasqua is part of Clinical Pharmacology and Discovery Medicine, GlaxoSmithKline, Greenford, United Kingdom.

Role of funding source:

This manuscript is part of a PhD research fellowship programme sponsored by GlaxoSmithKline, UK. GlaxoSmithKline had no further role in the research rationale, collection, analysis and interpretation of the data; in the writing of the report; and in the decision to submit the paper for publication.

In this particular study they assessed the sensitivity of the individual HAM-D17 items in differentiating responders from non-responders over the typical treatment period used in clinical efficacy trials. Based on data from randomised, placebo controlled trials with paroxetine, a graphical analysis and a statistical analysis were performed to identify the items that are most sensitive to the rate and extent of response irrespective of treatment.


It's very scientific in nature but when paroxetine is used in any study it raises an eyebrow, particularly from me. Even more so when part of the team doing the study work for the manufacturer of paroxetine.

Basically, paroextine is about as useful as a chocolate teapot but to hide that fact, this paper claims that the Hamilton Depression Scale is not sensitive enough to detect responders to their drug!

Paroxetine is useless so they don’t think the HAM-D scale should be used in its entirety – just those parts of it that make their drug look better than placebo.

Genius marketing once again from the boys of Glaxo.

Didn't Glaxo manipulate data in the 329 study too?

The paper can be downloaded here.

Fid


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Wednesday, April 22, 2009

Miami Herald Broward child's suicide raises questions about medication


Source: Miami Herald

A Broward foster child who killed himself last week had been prescribed powerful psychiatric drugs, some of which the FDA does not approve for children.


BY CAROL MARBIN MILLER
April 21, 2009

Gabriel Myers, the 7-year-old Broward boy who hanged himself in the shower of his foster home

Weeks before his death, Gabriel Myers, the 7-year-old Broward boy who hanged himself in the shower of his foster home, had been prescribed a powerful mind-altering drug linked by federal regulators to an increased risk of suicide in children.

In all, Gabriel had been prescribed four psychiatric drugs, two or three of which he was taking at the time of his death, said Jack Moss, Broward chief of the state Department of Children & Families. Moss said he is not sure which medications the boy was taking because Margate police took the foster home's medication log as part of an investigation into Gabriel's death last week.

Full story HERE

Fid


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Monday, April 06, 2009

SSRi - The Video


Fid


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

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Sunday, April 05, 2009

Evidence Why Seroxat Could be Deemed a Defective Drug

Coming Soon



Fid




Meantime... a short video.




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

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'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman

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