Via “Trudy Lieberman”:http://www.cjr.org/campaign_desk/a_laurel_to_the_milwaukee_jour.php at _Columbia Journalism Review,_ an “excellent story”:http://www.jsonline.com/features/health/95198129.html on the dubious linkages between medical academia and drug companies.
bq. Richard Page thinks Multaq is an excellent new drug for treating atrial fibrillation, a type of irregular heartbeat that affects more than 2 million Americans. And Page, chairman of the department of medicine at the University of Wisconsin School of Medicine and Public Health, should know. He co-authored a large, international study that led to the drug’s approval by the Food and Drug Administration last year, a move that could mean hundreds of millions in sales for Sanofi-Aventis, the company that makes the drug. But in putting his name on the influential paper, Page allowed Sanofi-Aventis to dictate the terms. He vouched for the accuracy and completeness of the study despite not seeing the raw data. The company, which paid for the study, collected that information and performed the analysis without an external audit for accuracy or completeness. Page says it comes down to trusting the drug company. “These companies, if they were falsifying data, wouldn’t be kept in business if that were found out,” he said. “I was satisfied and remain satisfied that the study was conducted in an appropriate way.” … In the Multaq case, Page and all six co-authors had financial ties to Sanofi-Aventis at the time of the study. Two authors worked for the company and owned its stock. Page and the four other authors moonlighted as consultants or speakers.
Genteelly corrupt relationships are a really big problem for medical research. The “Boston Review”:http://bostonreview.net/BR35.3/ndf_pharma.php has an “excellent forum”:http://bostonreview.net/BR35.3/ndf_pharma.php on this broad topic up on their website, including a quite preposterous “defense”:http://bostonreview.net/BR35.3/stossel.php by “Thomas P. Stossel”:http://www.sourcewatch.org/index.php?title=Thomas_P._Stossel of medical-industry research ties against _any_ suggestion that formal standards, requirements of transparency etc might be helpful.