Do you EVER read beyond the headlines, you intellectually dishonest POS?
David Graham, the associate director for science in FDA's office of drug safety, made the estimate based on 92.8 million U.S. prescriptions for Vioxx between 1999 and 2003. It's part of a study Graham conducted in cooperation with Kaiser Permanente.
Merck pulled Vioxx, a popular pain reliever widely used by arthritis patients, off the market in September, saying it was "putting patient safety first" but the Wall Street Journal reported earlier that company officials had fought for years to protect the highly profitable drug and to keep news of the health risks quiet.
The study found that high doses of Vioxx, or rofecoxib, tripled risks of heart attacks and sudden cardiac death. Graham planned to present the findings at an epidemiology conference Aug. 25, but his supervisors said the results were "too preliminary" and recommended that the study be submitted first to a medical journal so it could undergo peer review or be presented at the conference with an alternative FDA opinion.
When the study was presented Aug. 25, the abstract said, "[T]his and other studies cast serious doubt on the safety of rofecoxib ... and its use by physicians and patients" at doses exceeding 25 milligrams. "When Graham submitted a revised, final version to FDA on Sept. 30, FDA's announcement of the study's release did not mention specific data on cardiovascular risks.
About 20 million Americans had taken Vioxx by the time Merck withdrew it.
And then there's this from 2007:
http://www.nature.com/news/2007/071113/full/450324b.html
Merck has won 11 Vioxx cases so far, whereas plaintiffs have prevailed in only 5.
If you put out a drug you KNOW has a high risk of killing it's users, and people subsequently die, that is MANSLAUGHTER!
Do you comprehend THAT, bunky? But hey, they settled without admitting guilt, so your toadie ass can relax because no one YOU know died, right?
YOU disgust me.