“You could say these marketing tactics are merely concerning. But I think of them as satanic. What the data are telling us is that these drugs are ruining people’s lives,” said Phillip Prior, MD
Medicine has been derailed from its Hippocratic tradition, science has been utterly corrupted by commercial interests, and doctors are disregarding patients’ interests. Patients are losing ground, no longer do they have a choice about the medical treatments that they get, or finding an ethical doctor whose recommendations are not tainted…
The catalyst for Dr. Elliott’s article was the tragic case of Dan Markingson, a 26-year old who committed suicide in May 2004, while enrolled in the CAFE trial, prescribed Seroquel. This case encapsulates the tragic consequences of a broken system which is not designed to detect the hazards for human subjects posed by market-driven research.
ACRE’s mission is to persuade physicians that MORE rather than less industry involvement in Continuing Medical Education programs is good for patients–much as industry’s "Harry and Louise" ads were aimed at convincing the public that universal healthcare was BAD for them.
Medtronic acknowledged that some of the consulting payments occurred during the time that Dr. Kuklo, was shopping his favorable study of Medtronic’s Infuse bone-graft product to medical journals.
Given the serious charges against Dr. Kuklo–including fraud, forgery, and conducting an unapproved experiment on soldiers–the University of Washington’s failure to take action until a series of articles in The New York Times and pressure brought to bear by Sen. Charles Grassley, speaks volumes about a pervasive culture of arrogance in academia.
Colonel Coots: "It is a significant breach of academic protocol. It’s a breach of trust."
It may come as a shock to some of you; but, Electroshock machines have never been tested for safety or efficacy.
Like their benefactors–drug manufacturers–who violate the law, doctors will be prosecuted in court by the federal government.
Guidant Didn’t Disclose a Flaw in Defibrillator for 3 Years_NYT / FDA Wrong on Crestor Safety Tue, 24 May 2005 The New York Times reports that the maker a a heart defirillator knew for 3 years about a malfunction and failed to inform physicians about It because the company “had…
Guidant Case May Involve Crime Inquiry Thu, 29 Sep 2005 The New York Times reports that “criminal investigators at the Food and Drug Administration have apparently become involved in the agency’s inquiry into how the Guidant Corporation handled problems with its heart devices, said two people contacted by the investigators."…
“Orgasmatron” implant experiment – legitimate or dubious? Fri, 28 Nov 2003 The FDA has approved what one can only call a bizarre expriment to test a surgically implanted device (orgasmatron) in the spine, of women–ostensibly to treat “sexual dysfunction.” To implant the device, “wires connected to a battery pack are…
