Posts Tagged ‘GlaxoSmithKline’

Paxil Class Action Moves on in Canada as Lawsuits Still Filed in U.S.

Wednesday, January 2nd, 2013

The Legal Examiner
By Steve Thomas
January 2, 2013

Click image to read all drug warnings, studies and side effects reported to the FDA on the antidepressant drug Paxil

GlaxoSmithKline, maker of the selective serotonin reuptake inhibitor Paxil, is mired in a class action lawsuit in Canada that alleges the antidepressant caused birth defects in children whose expectant mothers took the drug without the corporation’s adequate warning of the heightened risks. A British Columbia judge permitted the class action.

This is the sort of thing that cost the manufacturer legal and financial setbacks in the U.S. The corporation spent millions on legal defense and paid millions in compensation awarded in Paxil lawsuits based on similar causes of action. The pharmaceutical litigation team at Reich & Binstock represents Paxil victims. The damage to children and to families frankly defies description, but the recovery of damages, including exorbitant medical costs, is welcome relief. Reich & Binstock’s personal injury attorneys are proud and fulfilled to help victims receive the justice they deserve.

Apparently, the Canadian mothers took the drug before warnings existed about the heightened risks of Paxil birth defects, such as a rare heart and lung condition known as persistent pulmonary hypertension — risks that the manufacturer should have known and had a duty to provide. Certainly bewildered women of childbearing age, who were taking either Paxil or another SSRI for that matter, wish they had known.

Imagine how they felt when their newborns were diagnosed with serious heart and lung conditions and then they learned that they and their babies were unwitting Paxil casualties. Put yourself upon careful reflection in such a mother’s shoes for a moment, as best you can.

The U.S. Food and Drug Administration in July 2006 updated its prescribing information for Paxil and for other SSRIs, including, Celexa, Fluvoxamine, Lexapro, Prozac, Symbyax and Zoloft. Those medications are in the same boat, and thank goodness there is a judicial process to redress the injuries associated with taking those drugs.

The FDA’s safety alert was based on a study that showed “infants born to mothers who took selective serotonin reuptake inhibitors after the 20th week of pregnancy were 6 times more likely to have persistent pulmonary hypertension than infants born to mothers who did not take antidepressants during pregnancy. The background risk of a woman giving birth to an infant affected by PPHN in the general population is estimated to be about 1 to 2 infants per 1,000 live births. Neonatal PPHN is associated with significant morbidity and mortality.”

Read full article here:  http://houston.legalexaminer.com/fda-and-prescription-drugs/paxil-class-action-moves-on-in-canada-as-lawsuits-still-filed-in-us.aspx?googleid=306286

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The Huffington Post—Drug Companies Drive the Psychiatric Drugging of Children

Tuesday, July 24th, 2012
The Huffington Post—July 24, 2012
by Dr. Peter Breggin, Reform Psychiatrist

(click image to visit the psychiatric drug database) “The health professions would do far more good stopping the drugging of children than continuing or increasing it. Ethical professionals need to work toward removing children from psychiatric drugs.” – Dr. Peter Breggin

July 24, 2012 – Johnson & Johnson, the company that makes the antipsychotic drug Risperdal, has tentatively agreed to a settlement of $2.2 billion to resolve a federal investigation into the company’s marketing practices. Although details are not fully finalized, this includes “a roughly $400 million criminal fine for the illegal promotion of the antipsychotic Risperdal,” according to the Wall Street Journal. It’s been well documented that Johnson & Johnson confidentially paid psychiatrists such as Harvard’s Joseph Biederman to promote adult drugs such as the powerful antipsychotic drug Risperdal for children. The company has even ghost-written at least one of the Harvard professor’s “scientific” articles.

Another recent DOJ settlement with drug company GlaxoSmithKline resulted in Glaxo’s agreement to pay $3 billion in criminal and civil fines. As I wrote in an earlier Huffington Post blog:

In one of the most egregious examples of fraudulent marketing, “In the case of Paxil, prosecutors claim GlaxoSmithKline employed several tactics aimed at promoting the use of the drug in children, including helping to publish a medical journal article that misreported data from a clinical trial,” [according to the New York Times].

Glaxo manipulated and rewrote this study, which was rejected by the FDA for failing to show efficacy. The Glaxo rewrite made it appear as though the drug was useful for adolescent depression even though the FDA had not approved Paxil for adolescents. The company then got almost two dozen well-known researchers and “experts” to put their names on the article as if they had written it.

GlaxoSmithKline also secretly paid about $500,000 to psychiatrist Charles Nemeroff, while he was a professor at Emory University, to promote Paxil

GlaxoSmithKline also secretly paid about $500,000 to psychiatrist Charles Nemeroff, while he was a professor at Emory University, to promote Paxil. Glaxo even ghostwrote a psychopharmacology textbook for family doctors, who write many prescriptions for children, which was “coauthored” by Nemeroff and psychiatrist Alan Schatzberg. Nemeroff was sanctioned for failing to report the Glaxo payments he received while at Emory. But he’s landed on his feet running, now chairing the psychiatry department at the Miller School of Medicine at the University of Miami.

None of these drug-company-bought psychiatrists has suffered serious consequences. Biederman remains a star at Harvard and Nemeroff recently received a new $2 million federal grant from the National Institute of Mental Health. These influential psychiatrists are just two out of many doctors who have been investigated for extensive financial relationships with drug companies.

Meanwhile, the DOJ has now enforced a total of $8.9 billion in criminal and civil fines against GlaxoSmithKline, Pfizer, Eli Lilly, and Johnson & Johnson.

Drug-company marketing has bought rich rewards, as reflected in the increasing numbers of children and youth diagnosed with attention deficit hyperactivity disorder and other psychiatric problems. According to the Centers for Disease Control (CDC), 12.3 percent of boys and 5.5 percent of girls age 5-17 were diagnosed with the disorder in 2009. With the rates growing especially rapidly in the older children, considerably more than 12.3 percent of older boys are given this diagnosis, which almost inevitably leads to treatment with stimulant drugs such as Ritalin, Concerta, Focalin, Dexedrine and Adderall. Given estimates of 2.8 million children taking stimulants for ADHD in 2008, the number is now well over three million and rising.

“Drug-company marketing has bought rich rewards, as reflected in the increasing numbers of children and youth diagnosed with attention deficit hyperactivity disorder and other psychiatric problems.” – Dr. Peter Breggin

Last year, the American Academy of Pediatrics overrode FDA drug guidelines and advised that children as young as 4 could be diagnosed with ADHD and treated with stimulants. This will surely increase the numbers of younger children psychiatrically diagnosed and medicated with other drugs as well. In our professional experience, children given stimulants may become the targets of additional drugs as their conditions worsen due to the stimulants. Stimulants have been the entering wedge into the widespread psychiatric drugging of America’s children. Once the door was opened, nearly all the other psychiatric drugs came rushing in.

Keep in mind that the more than three million children on psychiatric drugs are for only one class of medication — stimulants for ADHD. Large numbers of other children are being put on highly dangerous adult antipsychotic drugs, antidepressants, and mood stabilizers, often to treat so-called “childhood bipolar disorder.” Psychiatrist Biederman’s work “helped to fuel a controversial 40-fold increase from 1994 to 2003 in the diagnosis of pediatric bipolar disorder … and a rapid rise in the use of antipsychotic medicines in children,” according to the New York Times. Bipolar disorder, like most other psychiatric diagnoses for children, is linked to the greater use of various psychiatric drugs. No surprise that this is so, since as in the case of Joseph Biederman, the “top” researchers in child psychiatry are heavily funded by pharmaceutical companies.

It is our personal and professional opinion that most childhood psychiatric diagnoses have no scientific validity. ADHD, for example, is described and diagnosed by a collection of behaviors – inattention, impulsivity, and hyperactivity — that can be caused by innumerable factors including too high expectations for a child, confused parenting, family disintegration, racism and poverty, inadequate teaching, poor nutrition, bullying, and head injury. The diagnosis literally shuts down the search for the real causes, undermines effective parenting and teaching approaches, and guarantees that the child will be medicated.

As another example, oppositional defiant disorder (ODD) merely describes a child who displays anger. In the words of the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, ODD involves “A pattern of negativistic, hostile, and defiant behavior lasting at least six months.” The top three “symptoms” are “(1) often loses temper, (2) often argues with adults, and (3) often actively defies or refuses to comply with adults’ requests or rules.” That’s not a disease in a child, it’s a sign that something has gone haywire in the child’s life and is not being remedied.

My most recent review of the scientific literature in Psychiatric Drug Withdrawal concludes that stimulants, antidepressants and antipsychotic drugs are very harmful to the brain. With increasing millions of children being placed on drugs that can harm normal development of the child’s brain and mind, and substitute for proper teaching and parenting, it’s time to change emphasis. As a society, we need to resist the quick fix that does more harm than good, and to stand up against the massive drugging of children.

The health professions would do far more good stopping the drugging of children than continuing or increasing it. Ethical professionals need to work toward removing children from psychiatric drugs.

The health professions would make a major contribution to the wide-scale health of children not only by curtailing psychiatric drugging, but also by offering the opportunity for parents to withdraw their children from these psychoactive substances.

Peter R. Breggin, MD is a psychiatrist in private practice in Ithaca, New York, and the cofounder with his wife Ginger Breggin of the Center for the Study of Empathic Therapy. He is the author of dozens of scientific articles and more than twenty books. His latest book is Psychiatric Drug Withdrawal: A Guide for Prescribers, Therapists, Patients and Their Families. It is based on a Person-Centered Collaborative Approach to psychiatric treatment with the focus on psychiatric drug withdrawal. It also describes many of the most severe adverse effects of psychiatric drugs that require drug withdrawal.

Ginger Breggin, in addition to cofounding and managing the Center for the Study of Empathic Therapy, has coauthored books with her husband, contributes to their mutual research projects, and blogs independently on The Huffington Post.

Disclosure: Peter Breggin, M.D. has been a plaintiffs’ medical expert in product liability suits against the mentioned drug companies including Eli Lilly, Pfizer, GlaxoSmithKline, and Johnson & Johnson.

http://www.huffingtonpost.com/dr-peter-breggin/psychiatric-drugs_b_1693649.html

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Natural News: GlaxoSmithKline Bribery Admissions

Monday, July 16th, 2012

(NaturalNews) Radio personality Dr. Drew Pinsky once touted GlaxoSmithKline PLC’s antidepressant Wellbutrin as one of a few such medications he prescribed to patients suffering from depression because it “may enhance or at least not suppress sexual arousal” as much as other antidepressants.

What he didn’t tell listeners during that 1999 endorsement; however, was that two months earlier Dr. Pinsky – who rose to fame as “Dr. Drew,” co-hosting a popular radio sex-advice show, “Loveline” – received the second of two payments from GSK for a total of $275,000 for “services for Wellbutrin,” The Wall Street Journal reported.

The paper said the payments were made to Pinsky via a communications firm that worked for GSK, according to revelations in an attachment to a complaint filed by the U.S. government in October 2011 in a Massachusetts federal court. The documents were disclosed in early July after the Justice Department announced a $3 billion criminal and civil settlement with GSK over illegal medication marketing, among other things.

In an email response to an inquiry about the payments by the Journal, Pinsky said: “In the late ’90s I was hired to participate in a two-year initiative discussing intimacy and depression which was funded by an educational grant by Glaxo Wellcome,” one of the pharmaceutical firms that eventually merged into GlaxoSmithKline.

Pinsky added that the campaign he was involved with “included town hall meetings, writings and multimedia activities in conjunction with [a] patient advocacy group.”

“My comments were consistent with my clinical experience,” he concluded, according to the paper.

Revelations stem from Big Pharma fraud settlement

According to published reports, GSK pleaded guilty to promoting popular antidepressants Paxil and Wellbutrin for uses that had not been approved by U.S. drug licensing officials at the Food and Drug Administration.

In its original complaint, the federal government said GSK improperly promoted Paxil as safe for children and adolescents, though the FDA had never given its okay for such patients, and the company’s own clinical trials raised red flags over increased suicide risk concerns.

Federal prosecutors alleged that GSK promoted Wellbutrin for improper uses as well, which included treatment of attention deficit disorder, bipolar disorder, obesity, sexual dysfunction and anxiety, though it was never shown to have been safe or effective for such uses, The Associated Press reported.

The government’s complaint came on the heels of a nine-year investigation of GSK’s marketing practices, which led to the huge settlement.

As the Journal noted, physicians can prescribe medications as they deem appropriate, but it’s illegal for companies to promote a drug for any uses not approved by the Food and Drug Administration - a practice that’s known as “off-label” marketing.

In the case of Dr. Drew and Wellbutrin, the drug’s prescribing label says nothing about it being “less inhibiting of sexual libido than other antidepressants,” WSJ reported.

In an email to the paper earlier this month, GSK refused to answer questions about the company’s financial ties to Pinsky or any other physicians.

Taken out of context?

“The complaint to which you refer concerns events in 1999, 13 years ago. It does not reflect what would be allowed in GSK today,” a company spokesperson told the paper.

“The government has made many allegations and legal conclusions concerning Wellbutrin that GSK disputes,” the spokesperson continued. “GSK admits; however, that during the period from January 1999 to December 2003, there were some occasions in which certain GSK sales representatives, speakers, and consultants promoted its antidepressant Wellbutrin to physicians for uses which were not FDA-approved in violation of federal law.”

Pinsky, the paper said, is only one doctor mentioned in the government’s complaint. It also accuses other doctors of taking payments from GSK and improperly endorsing the company’s drugs. One doctor received $2 million from GSK between 2001 and 2003.

That physician, James Pradko, “gave hundreds of talks to doctors and Glaxo sales reps about depression and frequently made ‘off-label claims’ about Wellbutrin’s effectiveness against a number of conditions for which it isn’t FDA-approved, including weight loss, chronic fatigue syndrome, erectile dysfunction and chemical dependencies,” said WSJ.

In an telephone interview with the paper, Pradko said the U.S. government complaint takes the speeches he gave “very much out of context,” adding he only ever spoke about treating depression and that his speeches “weren’t meant to sell drugs, ever.”

Sources:

http://online.wsj.com

www.naturalnews.com/GSK.html

http://www.naturalnews.com

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How To Sell Drugs to Children — GlaxoSmithKline & Shrinks for Sale

Friday, July 6th, 2012
Fox Business
by Al Lewis – July 5, 2012

The international pharmaceutical giant took top-prescribing psychiatrists to pricey resorts in Bermuda, Jamaica, Hawaii and other exotic locales where, in between spa services, they could hear speeches from fellow shrinks that the company paid to dither on about how kids should pop its pills.

America’s children were depressed. They needed antidepressants. It was GlaxoSmithKline to the rescue.

Paxil was never approved for use by anyone under 18, but GlaxoSmithKline  had 1,900 sales reps visiting doctor’s offices, and pushing the drug for kids.

The international pharmaceutical giant took top-prescribing psychiatrists to pricey resorts in Bermuda, Jamaica, Hawaii and other exotic locales where, in between spa services, they could hear speeches from fellow shrinks that the company paid to dither on about how kids should pop its pills.

According to a criminal complaint filed in U.S. District Court in Massachusetts, the company “engaged in a fraudulent scheme to deceive and defraud physicians, patients, regulators, and federal health-care programs.” The complaint, alleging the company misbranded drugs and failed to report safety data, was filed under seal in October.

On Monday, the international pharmaceutical giant said it agreed to settle this case as well as a civil case for $3 billion. This the largest health-care fraud settlement in U.S. history, involving Paxil and some of its other drugs.

click image to find out more

GlaxoSmithKline said it will plead guilty to the criminal charges, which are misdemeanors, but it will not admit any wrongdoing on the civil charges, which allege potentially deadly behaviors that I think should be considered felonious.

I guess this is why corporate lawyers make the big bucks: To go to court and say, “Yes, we did it–but not if anyone else is trying to sue us.” It’s also worth noting that no single individual has been named as a defendant in the criminal complaint. It’s just another one of those unfortunate corporate things that nobody ever got caught doing.

The U.S. Justice Department’s complaint said the alleged offenses occurred between 1999 and 2010. The company’s chief executive, Sir Andrew Witty, reiterated that this was the behavior of the old company, not the one he is currently running.

“I want to express our regret and reiterate that we have learnt from the mistakes that were made,” Mr. Witty said in a statement released Monday. “Since I became CEO, we have had a clear priority to ingrain a culture of putting patients first, acting transparently, respecting people inside and outside the organisation and displaying integrity in everything we do.”

Yes, you spotted it. It’s the ol’, “mistakes were made” strategy from the PR playbook. The company’s mantra is “Do more, feel better, live longer.” But it might as well have been, “Prescribe Paxil to children. Win a free trip!”

GlaxoSmithKline’s Paxil push occurred between 1999 and 2003, the government alleged, and soon “Paxil became one of the top-selling drugs in the United States.”

Have you ever sat in doctor’s waiting room when an exceptionally well-dressed woman, looking like she could be a fashion model, struts through the door? That was the pharmaceutical rep. Or sometimes it’s a handsome guy who looks right out of GQ. This is how drugs, including Paxil, are sold. Beautiful people handing out free drug samples so doctors will prescribe them. Just look at me, and never mind all that fine print on the side effects.

GlaxoSmithKline "promoted Paxil for unapproved uses by bringing top-prescribing psychiatrists to lavish resorts.

Central to GlaxoSmithKline’s marketing effort for Paxil was an article published in Journal of the American Academy of Child and Adolescent Psychiatry that the government convincingly argues is “false and misleading.” GlaxoSmithKline reps touted this allegedly bogus research. GlaxoSmithKline also paid shrinks to give speeches in which they referenced it.

Here’s how the government describes these paid-shrink performances in it’s criminal complaint:

GlaxoSmithKline “promoted Paxil for unapproved uses by bringing top-prescribing psychiatrists to lavish resorts.

“The meetings were held at expensive resorts such as the El Conquistador Resort & Golden Door Spa in Puerto Rico, the Rio Mar Beach Resort in Hawaii, and the Renaissance Esmeralda Resort & Spa in Palm Springs, Calif. GSK paid for the psychiatrists’ lodging, air fare, and a $750 honorarium. GSK paid speakers a $2,500 honorarium. GSK also paid spouses’ airfare if two cheaper tickets were available for the cost of one full-coach fare.

“GSK hosted nice dinners…and paid for entertainment, including sailing, snorkeling, tours (e.g. the Bacardi rum distillery), golf, deep sea fishing, rafting, glass-bottomed boat rides, and balloon rides.

“The actor/comedian GSK hired to emcee one of the meetings told the attendees “We have a wonderful and unforgettable night planned. Without giving it all away, I can tell you–you’ll be experiencing a taste of luxury.” “After the May 2000 Forum meeting in Hawaii, one psychiatrist wrote: “A beautiful location, enjoyable and fun-filled activities, an exciting, cutting-edge informative educational program…exhilarating!” Another doctor wrote after the Forum 2001 meeting in Palm Springs: “Both my wife and I enjoyed the extra care our drug rep gave to us all weekend.’”

When the issue of certain side effects came up, the programs went something like this: “OK, so some of the kids who took Paxil had suicidal thoughts and killed themselves. Maybe it was an adverse reaction to the drug, or maybe they were just depressed. Depressed kids do depressing things, you know. It’s what we call ‘emotional liability.’ Meantime, please, enjoy the resort, and don’t miss that Bacardi rum tour!”

Maybe the reason kids are depressed is because of the way some of the highest-paid adults in this world behave.

(Al’s Emporium, written by Dow Jones Newswires columnist Al Lewis, offers commentary and analysis on a wide range of business subjects through an unconventional perspective.)
http://co106w.col106.mail.live.com/default.aspx#!/mail/InboxLight.aspx?n=434132513!n=219306126&fid=1&fav=1&mid=3217e4a4-c775-11e1-a160-00215ad9bc86&fv=1

 

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GlaxoSmithKline Admits to Criminal Pharma Fraud in 3 Billion Dollar Case

Thursday, July 5th, 2012

In related news on this case – also read “Has Dr. Drew Been Pimping Wellbutrin to his Listeners for GlaxoSmithKline?” http://goo.gl/uZadq

Natural News – July 4, 2012

by D. Holt

British registered company, GlaxoSmithKline, faces $3 billion in penalties after pleading guilty to the biggest health care fraud case in history. GSK admitted that physicians had been bribed to push potentially dangerous drugs in exchange for Madonna tickets, Hawaiian holidays, cash and lucrative speaking tours. They also admitted distributing misleading information regarding the antidepressant Paxil. The report claimed that it was suitable for children, but failed to acknowledge data from studies proving its ineffectiveness in children and adolescents.

GSK faced charges that they had used the gifts to sell three drugs that were either unsafe, or used for purposes that were not approved. The first drug, Paxil also known as Seroxat, was touted as safe and effective for children and adolescents. The ineffectiveness of Paxil, and the link to suicides, meant that it was banned for kids under 18-years-olds in 2008.

The second drug, Avandia was used in Britain to treat diabetes until it was withdrawn due to safety fears, including increased risk of heart attacks. The US government claimed that GSK had attempted to conceal the data surrounding the dangers.

The third drug, Wellbrutin is used in the UK for treating depression, but it was alleged that GSK had recommended physicians used it for ADHD, lost libido and as a slimming aid. None of which were approved uses for the drug.

The moral code of Big Pharma companies exposed

Sir Andrew Witty, chief executive of GSK said “Whilst these offenses originate in a different era for the company, they cannot and will not be ignored. On behalf of GSK, I want to express our regret and reiterate that we have learned from the mistakes that were made. We are deeply committed to doing everything we can to live up to and exceed the expectations of those we work with and serve. In the US, we have taken action at all levels in the company. We have fundamentally changed our procedures for compliance, marketing and selling.”

US attorney for Massachusetts, Carmen Ortiz said: “The GSK sales force bribed physicians to prescribe GSK products using every imaginable form of high priced entertainment, from Hawaiian vacations to paying doctors millions of dollars to go on speaking tours, to a European pheasant hunt, to tickets to Madonna concerts.”

This is the biggest settlement in the history of drug industries, ahead of the 2009 Pfizer case in which it was fined $2.2 billion for promoting four drugs for unapproved uses. In 2010, GSK paid $96 million to a whistle-blower who exposed contamination problems and a management cover up in Puerto Rico.

The practice of pushing drugs for unapproved uses is endemic within the drug industries. Two of the largest drug companies have been caught and fined huge amounts for chasing sales targets using any means necessary. It proves that the health of customers, even children, ranks lower on the companies’ agenda than profit. Using bribes to get doctors to prescribe drugs shows a complete lack of moral fiber from both sales teams and the doctors. After this case, surely the doctors also need to face the courts for their conduct.

Whilst the amounts of money seem to be a huge punishment for GSK, the settlement is merely a slap on the wrist for a company whose market value is $133 billion. Can we trust another multinational that promises to clean up its act, when others have promised the same, only to behave just as recklessly but much more surreptitiously.

Sources for this article include:

http://www.dailymail.co.uk

http://www.nytimes.com
http://www.cbsnews.com
http://bottomline.msnbc.msn.com

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Feds Say Dr. Drew Was Paid By Glaxo To Talk Up Antidepressant

Tuesday, July 3rd, 2012

Forbes
By Matthew Herper – July 2, 2012

Dr. Drew Pinsky (Photo credit: Randy Stewart)

Part of the case made by U.S. prosecutors that led to GlaxoSmithKline’s $3 billion settlement today is that the company used a network of paid experts, speaking to doctors and to the press, to promote uses of its drugs that had not been approved by the Food and Drug Administration. According to the Department of Justice’s complaint, one of those paid experts was celebrity physician Dr. Drew Pinsky, then the host of the radio show Loveline, which was also being broadcast on MTV. Pinsky has gone on to host Celebrity Rehab, Dr. Drew on HLN, and Dr. Drew’s Lifechangers on the CW.

The government alleges that Pinsky was paid a total of $275,000 over just two months – March and April 1999 – to deliver messages about Wellbutrin SR, a Glaxo antidepressant, “in settings where it did not appear that Dr. Pinsky was speaking for GSK.”

As an exhibit to the complaint, the prosecutors  include invoices from Cooney Waters, a public relations firm, to GlaxoSmithKline for Pinsky’s services as a spokesperson. They also include a transcript of Pinsky’s appearance on David Essel – Alive!, another national radio program. As part of the $3 billion settlement announced today, Glaxo agreed to pay $727 million in criminal fines for its marketing of Wellbutrin SR and Paxil, another antidepressant.

One difference between Glaxo’s Wellbutrin SR and other antidepressants is that it may not decrease libido and may actually boost sex drive. (The drug’s package insert lists both “decreased libido” and “increased libido” as potential side effects.) Most common antidepressants, like Eli Lilly’s Prozac, Pfizer’s Zoloft, and Glaxo’s own Paxil, all of which are known as selective serotonin reuptake inhibitors (SSRIs), tend decrease sex drive. But Glaxo had no FDA approval for promoting Wellbutrin as having fewer sexual side effects. So it allegedly paid speakers, like Pinksy, who spoke about how, in his clinical practice, he used Wellbutrin SR in patients who suffered low sex drive on other drugs.

According to the transcript, the Essel show began with a clip from a woman who said she had 60 orgasms in a row, “just nonstop.” When asked if this was even possible, Pinsky replied, “Oh yeah. For some women. What I think she was amazed about was it just suddenly started and that kind of thing most typically happens from medication, frankly.” He then segues into saying that that is what he is on the show to talk about. Soon he’s talking about how Wellbutrin (he also mentions the generic name, bupropion) is the medicine he’s had the most experience with in his practice when it comes to avoiding the sexual side effects of antidepressants. “It actually is the one we advocate, one of the things we suggest people do if they’re getting a decrease in their libido or decrease in their arousal which typically occurs in the serotonin re-uptake inhibitor medication.”

 

The section of the government's complaint that details Glaxo's relationship with Dr. Drew. (Click to enlarge)

A note from the PR firm accompanying the transcript says: “During the fifteen-minute segment, Dr. Pinsky communicated key campaign messages.” The spot is almost a textbook for the way drug companies have used speakers to promote medicines. Everything Pinksy says is reasonable – anecdotally, Wellbutrin does seem to have few sexual side effects. But Pinsky’s comments has the effect of giving air time to a use of a medicine that Glaxo was not supposed to promote.

Dr. Drew wasn’t alone. He’s one of a long list of experts listed in the complaint that the government says were paid by Glaxo as part of its promotional efforts. Requests for comment were sent to a manager for Pinsky, a publicist who had represented him, and through his HLN web site, but were not immediately returned.

The documents:

The complaint

A transcript of Dr. Drew’s appearance on a radio show

Invoices to Glaxo from the public relations firm Cooney Waters for paying Dr. Drew’s speaking fees.

Other documents included in the DOJ’s complaint

Read article here:  http://www.forbes.com/sites/matthewherper/2012/07/02/feds-say-dr-drew-was-paid-by-glaxo-to-talk-up-antidepressant/

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US health agency revises conflict of interest rules

Tuesday, August 23rd, 2011

From Project on Government Oversight:

In recent years, Senator Grassley exposed several academic physicians for taking large amounts of money from companies with a direct financial interest in their research, some of it funded by the NIH. The list reads like a who’s who in academic research:

    • Dr. Charlie Nemeroff, former Chair of the Psychiatry Department at Emory University, who failed to report hundreds of thousands of dollars in payments from GlaxoSmithKline while researching that same company’s drugs with an NIH grant.  Dr. Nemeroff was bounced from Emory and has now taken over the Chair of Psychiatry at the University of Miami.
    • Dr. Alan Schatzberg, former Chair of the Psychiatry Department at Stanford University received an NIH grant to study a drug while partially owning a company that was seeking FDA approval of said drug. An NIH oversight group recommended that Stanford’s clinical trial on mifepristone be “terminated immediately and permanently.”  The recommendation was made because of concerns over conflicts of interest, patient safety and other issues.
    • Dr. Joseph Biederman and two other researchers at Harvard University failed to report almost a million dollars each in outside income while heading up several NIH grants. Harvard later disciplined the three physicians.

US health agency revises conflict of interest rules

From Reuters – August 23 – 2011

by  Alina Selyukh

WASHINGTON,  – The U.S. National Institutes of Health revised on Tuesday its 16-year-old conflict of interest rules for medical researchers, lowering the amount of money that constitutes a financial conflict and expanding the required disclosures.

The 1995 regulations effectively put responsibility for tracking scientists’ financial conflicts of interest on their universities. The rule required researchers to disclose conflicts to their institutions, which then had to assure the NIH the conflict had been managed, reduced or eliminated.

The new rule extends that requirement so researchers report not only the fact of a conflict of interest, but also its details such as value, specific nature, why it is a conflict and the impact it might have on research.

It lowers the amount a researcher must disclose if received from an industry or held in company stock to $5,000 from about $10,000.

Research institutions, in turn, are now required to report that information to the federal grant-awarding agency alongside details of how the conflicts are managed. Also, before spending any grant money, the institution has to post information about the financial conflicts on a public website.

The new rules will affect about 2,000 organizations that are awarded public health science funding every year and some 38,000 scientists who participate in research funded by these grants and have a “significant financial interest,” NIH said.

Concern about the integrity of research in the United States has grown since 2008, when Iowa Republican Sen. Charles Grassley criticized prominent Harvard University psychiatrist Dr. Joseph Biederman and others for failing to fully disclose payments from drug companies.

In a more recent example, medical device maker Medtronic Inc (MDT.N) came under fire over accusations that doctors paid by the company had failed to disclose major side effects from a bone growth drug in clinical trials.

A 2009 report by the Institute of Medicine, one of the National Academies of Sciences that advises U.S. policymakers, called on doctors to strictly disclose research funding to strengthen protection against conflicts of interest. The report called for virtually anyone involved in medicine — academic medical centers, journals, professional societies, researchers and doctors — to set up or strengthen conflict of interest guidelines.

From 1996 to 2007, relationships between individual academic researchers and industry nearly doubled, according to a study cited by NIH in its final rule. From 1994 to 2003, the amount of financial support for biomedical research almost tripled to $94.3 billion, with 57 percent of that funding coming from industry sources, according to analysis cited by NIH. (Additional reporting by Anna Yukhananov; editing by Andre Grenon)

http://www.reuters.com/article/2011/08/23/health-science-conflicts-idUSN1E77M1PB20110823

 

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Pharma-Funded Psychiatrists Behind Bogus Child ‘Bi-Polar’ Epidemic- Disciplined for Conflicts of Interest

Friday, July 22nd, 2011

Harvard Psychiatrists Disciplined for Conflicts of Interest

Alliance for Human Research Protection – July 21, 2011

by Vera Sherav

Psychiatrist Joseph Biederman was funded millions by Pharma while promoting child "bipolar" disorder

The primary promoters–inventors, one might say– of diagnosing children with “bipolar” disorder, who for over a decade, aggressively promoted the biopolar diagnosis and use of antipsychotics in children, were disciplined by Harvard University and its affiliated Massachusetts General Hospital.

An investigation, prompted by Sen. Charles Grassely, was conducted by Harvard University-affiliated Massachusetts General Hospital. It concluded (earlier this month) that psychiatrist Joseph Biederman and two of his proteges, Thomas Spencer and Timothy Wilens -each of who failed to disclose millions of dollars they had each received from the makers of antipsychotics, the drugs they promoted for the treatment of bipolar in children–had indeed violated the University’s/ and hospital’s conflict of interest reporting  standards.

The three wrote a mea culpa letter stating “we want to offer our sincere apologies…” acknowledging “our mistakes…”

However, no mention was made anywhere about the profound consequences of these psychiatritsts’ commercially-driven clinical recommendations. No mention about the corruption of the scientific literature, about clinical practice that deviated from the Hippocratic Oath, “First, do no harm,” nor was any mention made about the harm suffered by children whose doctors were misled about the safety and efficacy of highly toxic drugs.

Child psychiatrists and pediatricians throughout the US were guided by these exceedingly influential Harvard psychiatrists.

As Sen. Chuck Grassley noted in 2008 in the Congressional Record, “they are some of the top psychiatrists in the country, and their research is some of the most important in the field. {But] They have also taken millions of dollars from the drug companies.”

The companies that paid them millions include: Eli Lilly, Johnson & Johnson, Pfizer, GlaxoSmithKline and Bristol-Myers Squibb.

The Senator brought public attention–and to Harvard University administrators’ attention–the financial conflicts of interest, “Out of concern about the relationship between this money and their research.”

Indeed, documents uncovered during litigation confirmed that the research was scientifically corrupt and commercially-driven. The New York Times reported that Dr. Biederman promised Johnson a& Johnson that a study (yet to be conducted) in preschool children who would be given the company’s antipsychotic, Risperdal (risperidone) “will support the safety and effectiveness of Risperdal in this age group.”

“The psychiatrist, Dr. Joseph Biederman, outlined plans to test Johnson & Johnson’s drugs in presentations to company executives. One slide referred to a proposed trial in preschool children of risperidone, an antipsychotic drug made by the drug company. The trial, the slide stated, “will support the safety and effectiveness of risperidone in this age group.”

Dr. Biederman was the lead author of a trial published last year concluding that treatment with risperidone improved symptoms of attention deficit and hyperactivity disorder in bipolar children.”

Another of Biederman’s Harvard ignoble disciples was Jeff Bostic, who is also at Massachusetts General Hospital. He was named in a 2009 lawsuit joined by the US Department of Justice alleging Forest Laboratories promoted its antidepressants for pediatric use without FDA approval and paid kickbacks to docs to encourage prescriptions. He received $750,000 in payments for giving talks on using these drugs in children.

Strangely, the National Institute for Mental Health, which had awarded thse psychiatrists millions of dollars at taxpayers expense. It appears that NIMH officials did not see fit to even conduct an investigation into the corruption of science and violation of federal regulations. This demonstrates a lack of professional and moral integrity at the NIMH whose administrators think nothing about the misappropriation of public money for commercially-driven, junk research.

http://www.ahrp.org/cms/content/view/828/9/

Backstory from Pharmalot:

Pharmalot

Harvard Docs Disciplined For Conflicts Of Interest

By Ed Silverman // July 2nd, 2011 // 9:03 am

Three years after they were fingered in a US Senate probe into the interplay between academics who receive grant money from both pharma and the National Institutes of Health, three prominent psychiatrists from Harvard Medical School and Massachusetts General Hospital have been sanctioned for violating conflict of interest rules and failing to report the extent of their payments.

In a mea culpa addressed to their colleagues, Joseph Biederman, Thomas Spencer and Timothy Wilens wrote that “we want to offer our sincere apologies to HMS and MGH communities…We always believed we were complying in good faith with the institutional polices and our mistakes were honest ones. We now recognize that we should have devoted more time and attention to the detailed requirements of these policies and to their underlying objectives.”

And what is their punishment? They must refrain from “all industry-sponsored outside activities” for one year; for two years after the ban ends, they must obtain permission from the med school and the hospital before engaging in any of these activities and they must report back afterward; they must undergo certain training and they face delays before being considered for promotion or advancement (you can read their letter here).

The hospital had this to say: “A committee at Massachusetts General Hospital that has been looking into conflict-of-interest questions involving three MGH child psychiatrists has completed its review. Appropriate remedial actions have been taken by the hospital to address specific issues (read the statement). And a Harvard Med School spokesman sent us this: “We confirm that the review of their compliance with the Harvard Medical School Policy on Conflicts of Interest and Commitment has concluded, and appropriate actions have been taken.” He added that the conflicts policy was revised last year.

The sanctions result from a long-standing controversy over the explosive use of antipsychotics in children. Biederman, in particular (see photo), had been one of the most influential researchers in child psychiatry. Although his studies were small and often financed by drugmakers, his work helped fuel a 40-fold increase from 1994 to 2003 in the diagnosis of pediatric bipolar disorder.

For more than a decade, Biederman and his colleagues aggressively promoted the diagnosis and use of antipsychotics to treat childhood bipolar disorder, a problem that once was largely believed to be confined to adults. But the docs maintained this was underdiagnosed in kids and the meds could be used for treatment, even though they had not been approved for most pediatric use at the time. Meanwhile, the relationships with drugmakers were never properly disclosed (back story).

And for years, payments they received from drugmakers were not thoroughly reported to university officials. Yet, millions of dollars in NIH grants, which were administered by the hospital, were awarded to the docs at the same time they were receiving money from various drugmakers that make and sell antipsychotics and antidepressants. Which ones? Eli Lilly, Johnson & Johnson, Pfizer, GlaxoSmithKline and Bristol-Myers Squibb.

At one point, Biederman pushed J&J to fund a research center at MassGen that would focus on the use of its Risperdal antipsychotic in children, well before the med was approved for pediatric use. He was then placed in charge of the institute and began a study of 40 children between 4 and 6 years old who were given Risperdal and Lilly’s Zyprexa, another antipsychotic. At the time, Harvard and MGH rules forbid researchers from running trials with drugmakers if they receive more than $10,000 from a company that makes the drug (back story).

But in June 2008, US Senator Chuck Grassley made a far-reaching statement before Congress that pulled the curtain back on the money involved. The statement is memorialized in the Congressional Record. Referring to the three docs, he said “they are some of the top psychiatrists in the country, and their research is some of the most important in the field. They have also taken millions of dollars from the drug companies.”

“Out of concern about the relationship between this money and their research, I asked Harvard and Mass General Hospital last October to send me the conflict of interest forms that these doctors had submitted to their institutions. Universities often require faculty to fill these forms out so that we can know if the doctors have a conflict of interest. The forms I received were from the year 2000 to the present. Basically, these forms were a mess. My staff had a hard time figuring out which companies the doctors were consulting for and how much money they were making.”

How much were they making? At first, maybe a couple of hundred thousand dollars combined. But at his behest, the med school and hospital asked the docs to take a second look. “And this is when things got interesting. Dr. Biederman suddenly admitted to over $1.6 million dollars from the drug companies. And Dr. Spencer also admitted to over $1 million. Meanwhile, Dr. Wilens also reported over $1.6 million in payments from the drug companies.

“The question you might ask is: Why weren’t Harvard and Mass General watching over these doctors? The answer is simple: They trusted these physicians to honestly report this money.” And as Grassley then noted, there was still more money that went unreported (to read the Congressional record, click here and then check the box for 2008 and type in the name ‘Biederman’ in the search box. Then click on ‘payments to physicians’ to read the complete statement and the chart showing payments to each doc).

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Beware the ghost(writer)s of medical research

Friday, June 17th, 2011

The One Click Group – June 16, 2011

By Dr. Marc-André Gagnon
and Dr. Sergio Sismondo
Expert Advisors – EvidenceNetwork.ca

The medical research world has been concerned about the problem of ghostwriting for more than a decade.

The issue has been repeatedly raised in the mainstream media over the past few years, with most of the commentary focused on the ethics of academics serving as authors on papers they did not write and on some of the most egregious actions by pharmaceutical companies.

But these efforts miss the ways in which Big Pharma has developed new forms of medical research to serve its own interests.

How ghostwriting feeds Big Pharma profits

Big Pharma firms spend twice as much on promotion as on research and development (R&D). But it is worse than that: more and more medical R&D is organized as promotional campaigns to make physicians aware of products. The bulk of the industry’s external funding for research now goes to contract research organizations to produce studies that feed into large numbers of articles submitted to medical journals.

Internal documents from Pfizer, made public in litigation, showed that 85 scientific articles on its antidepressant Zoloft were produced and coordinated by a public relations company. Pfizer itself thus produced a critical mass of the favourable articles placed among the 211 scientific papers on Zoloft in the same period. Internal documents tell similar stories for Merck’s Vioxx, GlaxoSmithKline’s Paxil, Astra-Zeneca’s Seroquel, and Wyeth’s hormone-replacement drugs.

To promote the now-notorious Vioxx, Merck organized a ghostwriting campaign that involved some 96 scientific articles. Key ones did not mention the death of some patients during clinical trials. Through a class action lawsuit against Vioxx in Australia, it was discovered that Elsevier had created a fake medical journal for Merck – the AustralasSian Journal of Joint and Bone Medicine – and perhaps 10 other fake journals for Merck and other Big Pharma companies.

In another example, GlaxoSmithKline organized a ghostwriting program to promote its antidepressant Paxil. According to internal documents made public in 2009, the program was called “Case Study Publication for Peer-Review”, or CASPPER, a playful reference to the “friendly ghost”. Such strategies are not exceptions; they are now the norm in the industry. Most new drugs with blockbuster potential are introduced accompanied by 50, 60, or even 100 medical journal articles. Any firm that refused to play this game in the name of ethics would likely lose market share. Profits in the pharmaceutical industry depend on companies’ capacity to influence medical knowledge and create market share and market niches for their products.

A call for Evidence-Based medicine

In 2008, research showed that pharmaceutical companies systematically failed to publish negative studies on their SSRIs, the Prozac generation of antidepressants. Of 74 clinical trials, 38 produced positive results and 36 did not: 94 per cent of the positive studies were published, but only 23 per cent of the negative ones were, and two-thirds of those were spun to make them look more positive.

Physicians reading the scientific literature got a biased view of the benefits of SSRIs. This helps to explain the huge number of antidepressant prescriptions, in spite of the fact that, according to a meta-analysis in JAMA in January 2010, for 70 per cent of people taking SSRIs, the drug did not bring more benefits than a placebo. Compared to placebo, however, SSRI antidepressants can result in serious adverse drug reactions.

There we see one of the problems with the ghost management of medical research and publication. Pharmaceutical companies want upbeat reports on their drugs. They design, write, and publish studies that are likely to show their drugs in positive lights – and there are myriad ways to do so. Ghosts sometimes bend the truth, and sometimes even commit fraud, with grave results.

Why do academics serve as authors on scientific articles they did not write, using research they did not perform? Because they are rewarded, both by their universities and by their colleagues for how much they publish and for its prominence. Pharmaceutical companies and their agents are very good at placing articles in prestigious journals, and then make them even more prominent by having their armies of sales reps circulate them and talk them up.

Researchers who serve as authors on studies and analyses (perhaps scientifically correct) that are favourable to the industry can expect to see these articles increase their prestige and influence, and possibly even funding.

What happens, however, when a researcher produces studies and analyses (also scientifically correct) showing that some products are dangerous or inefficient, as some did about Vioxx before the scandal broke? Reading Merck’s internal e-mails, revealed during the class lawsuit, it was exposed that the company drew up a hit list of “rogue” researchers who needed to be “discredited” or “neutralized” – “seek them out and destroy them where they live,” reads one e-mail. Eight Stanford researchers say they received threats from Merck after publishing unfavourable results.

Corporate science

In the ghost management of research and publication by drug companies we have a new model of science. This is corporate science, done by many unseen workers, performed for marketing purposes, and drawing its authority from traditional academic science. The high commercial stakes mean that all of the parties connected with this new corporate science can find reasons or be induced to participate, support, and steadily normalize it. It also biases the available science by pushing favourable results and downplaying negative ones – and sometimes through outright fraud.

As long as pharmaceutical companies hold the purse strings of medical research, medical knowledge will serve to market drugs, not to promote health. And as long as universities grovel for more partnerships with these companies, the door will remain wide open to proceed with the corruption of scientific research.

http://www.theoneclickgroup.co.uk/news.php?id=6349#newspost

Dr. Marc-André Gagnon is assistant professor with the School of Public Policy and Administration at Carleton University. He is also an expert advisor with EvidenceNetwork.ca, a comprehensive and non-partisan online resource designed to help journalists covering health policy issues in Canada. Dr. Sergio Sismondo is professor of Philosophy and Sociology at Queen’s University. His current research is on the pharmaceutical industry’s relationships with academic medicine and practicing physicians.


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Feds Want Glaxo Exec To Testify In Stevens Case

Monday, April 25th, 2011

Pharmalot – April 25, 2011

By Ed Silverman

gavel-flickr4The trial of former GlaxoSmithKline lawyer Lauren Stevens gets under way this week and federal prosecutors hope to force a Glaxo exec to testify, according to documents filed in federal court last week. The feds are trying to compel James Millar, a vp of strategic pricing, contracting and marketing to take the stand in their quest to convict Stevens of obstruction of justice.

Stevens, you may recall, was first indicted last November for obstructing an FDA probe into off-label marketing of the Wellbutrin SR antidepressant and making false statements to the agency. More recently, the indictment was tossed, because prosecutors incorrectly portrayed her defense to a grand jury. However, they subsequently issued another indictment earlier this month (back story).

The feds want Millar to be compeled to testify because his testimony “may be necessary to the public interest.” However, prosecutors expect that he would refuse to testify or otherwise provide any info on the basis of his privilege against self-incrimination, according to court documents (read this). As of this morning, the order compelling his testimony has not been filed with the court.

As indicated previously, the trial threatens to evolve into a spectacle where Glaxo execs and Glaxo lawyers – notably, the King & Spalding law firm that frequently represents the drugmaker – turn the courtroom into a finger-pointing match among people who once labored on the same side of the pharmaceutical battlefield (see here).

http://www.pharmalot.com/2011/04/feds-want-glaxo-exec-to-testify-in-stevens-case/

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