It appears that the FDA and the pharmaceutical industry had a paddy-cake relationship in recent years. Rather than acting as regulators, government agencies have been more "cooperative" with business under the Bush administration. The problem? This kind of "regulation" doesn't safeguard the public's health.
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Seven weeks before Merck pulled Vioxx off the market, a Food and Drug Administration medical safety officer presented warnings to his bosses that the drug increased the risk of heart attacks.
But the author of that study, Dr. David Graham, reportedly has told Senate investigators that he was pressured by FDA management to water down his conclusions after he told the agency of them on Aug. 11.
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Questions for debate:1.)Why is it that mutually cooperative or voluntary regulation models inevitably leads to a compromising of health and safety?
2.)Is what happened at the FDA proof of the influence that the pharmaceutical industry exercises through political donations?
3.)Should government agencies have a more "attack dog" attitude towards the businesses they regulate?