More Big Pharma Fraud

Pharma Giant Funded their Own Study Claiming Drug Was Safe for Kids — It was Actually Deadly

By Jay Syrmopoulos on October 10, 2015

image: http://tftppull.freethoughtllc.netdna-cdn.com/wp-content/uploads/2015/10/paxil-gsk.jpg

paxil-gsk-2

Under current U.S. law, pharmaceutical companies are required to only market and advertise their drugs for FDA approved conditions.

Big pharma heavy-hitter GlaxoSmithKline (GSK) illegally influenced doctors to prescribe the antidepressant drug paroxetine (sold under the brand name Paxil) to teenagers and kids for years even though it was not FDA approved for use in adolescents.

Not to be discouraged by pesky laws, GSK began a focused marketing blitz aimed at doctors, which was a huge success with over 2 million Paxil prescriptions being written for kids in 2002 alone.

So why did doctors write over 2 million Paxil prescriptions for children when the drug was not even approved by the FDA for use in kids?

GlaxoSmithKine actually funded a research study that was published in 2001, known as Study 329, which claimed to show that the drug was “well tolerated and effective” in children.

A subsequent study, not funded by the pharmaceutical company, had drastically different conclusions as to the effectiveness and safety of Paxil in adolescents.

According to a report by Vox:

A major new analysis of the raw data behind Study 329, published in BMJ, suggests that the original conclusions were wildly wrong. Not only is Paxil ineffective, working no better than placebo, but it can actually cause serious side effects, including self-injury and suicide.

The New York State Attorney General’s office eventually found out what was going on with Paxil (and fraudulent activities related to other GSK drugs), sued GSK, and the company pleaded guilty to the wrongdoing, paying out $3 billion in fines. Through legal discovery, it became clear that the company knew their data on Paxil for teens was problematic, even hiring a PR firm to ghostwrite Study 329. In 2004, the FDA added an explicit “black box warning,” recommending against Paxil’s use in adolescents.

The researchers also found that Study 329 was fundamentally flawed. Researchers drastically downplayed serious risks and harms in their analysis of the drug, while intentionally manipulating their data.

To put this entire episode in perspective, GlaxoSmithKline not only created intentionally misleading “scientific” research, but attempted to use this misleading study to get doctors to prescribe its anti-depressant – to kids – for “off-label” use. The entire time GSK knew that the drug had no more benefit to children than a placebo and could lead to suicide and self-harm.

While GSK was massively fined for marketing Paxil to adolescents, drug companies are attempting change the current law to allow them to promote their products for uses that have not been approved by the FDA.

Two companies have sued the FDA, claiming that the current law violates their First Amendment right to free speech.

In August, a federal court in New York ruled in favor of one of the companies, Amarin, which sought to market its prescription fish oil for off-label uses.

A second company filed a similar lawsuit arguing that it should be allowed to promote its post-surgery pain drug for uses that are much broader than those authorized by FDA, according to Vox.

Writing for the Boston Globe, Ed Silverman explained the reality being faced.

“Beyond matters of constitutional law and governmental oversight, the pharmaceutical industry is clearly angling to boost prescription sales. Of course, this would fatten bottom lines, a good thing if you happen to be a shareholder,” Silverman said.

If pharmaceutical companies are successful in changing the law, it could potentially have major implications for public health and safety. The ability of patients and doctors to discern the difference between slick marketing ploys and evidence-based science may become even more difficult than it is already if the drug companies get their way.

Please share this story to help wake people up to the big pharma rip off!

Jay Syrmopoulos is an investigative journalist, free thinker, researcher, and ardent opponent of authoritarianism. He is currently a graduate student at University of Denver pursuing a masters in Global Affairs. Jay’s work has been published on Ben Swann’s Truth in Media, Truth-Out, AlterNet, InfoWars, MintPressNews and maany other sites. You can follow him on Twitter @sirmetropolis, on Facebook at Sir Metropolis and now on tsu

One response to this post.

  1. Posted by Nafsica (Sasa) Kelly on December 16, 2015 at 10:48 am

    Psychiatrists can’t predict what adverse side effects you might experience because not one of them knows how their drugs work.
    Psychotropic drugs are increasingly being exposed as chemical toxins with the power to kill. Psychiatrists claim their drugs save lives, but according to their own studies, psychotropic drugs can double the risk of suicide. And long-term use has been proven to create a lifetime of physical and mental damage, a fact ignored by psychiatrists.
    Common and well-documented side effects of psychiatric drugs include mania, psychosis, hallucinations, depersonalization, suicidal ideation, heart attack, stroke and sudden death.
    Not only that, but The US Food and Drug Administration admits that probably one to ten percent of all the adverse drug effects are actually reported by patients or physicians. 
    Protect yourself with the truth. Find out what psychiatrists don’t want you to know.

    Reply

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