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Vioxx News Article
February 25, 2005
The New York Times, "10 Voters on Panel Backing Pain Pills Had Industry Ties"

          Ten of the 32 government drug advisers who last week endorsed continued marketing of the huge-selling pain pills Celebrex, Bextra and Vioxx have consulted in recent years for the drugs' makers, according to disclosures in medical journals and other public records.
         If the 10 advisers had not cast their votes, the committee would have voted 12 to 8 that Bextra should be withdrawn and 14 to 8 that Vioxx should not return to the market. The 10 advisers with company ties voted 9 to 1 to keep Bextra on the market and 9 to 1 for Vioxx's return.
         Researchers with ties to industry commonly serve on Food and Drug Administration advisory panels, but their presence has long been a contentious issue. The agency has said it tries to balance expertise - often found among those who have conducted clinical trials of the drugs in question or otherwise studied them - with potential conflicts of interest.
Several of the panel members flagged with conflicts said most or all of the money went not to themselves but to their universities or institutions.
           Merck has made no decision on whether it will reintroduce Vioxx.
           Dr. Alastair Wood, an associate dean at Vanderbilt University and the panel's chairman, said he was disappointed that the F.D.A. failed to disclose the financial conflicts of the panel's participants before each day's meeting.
           Still, Dr. Wood said that even with its conflicts the panel was a tough critic of the drugs. Many of the panel members who were among the narrow majorities approving continued marketing of Bextra and Vioxx did so only with the stipulation that severe restrictions be imposed on their uses, he noted.
          He said he expected that the uses of the drugs would be confined to very limited patient populations.


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Persons living outside the United States who have been injured by an American product manufactured may also in certain cases file Vioxx lawsuits for compensation for heart attacks and strokes in United States courts.

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Vioxx Recall: The international prescription drug company Merck announced in September 2004 the worldwide withdrawal of the arthritis medication Rofecoxib, sold in most countries under the brand name Vioxx, because a study showed an increased risk of heart attack and stroke.

Vioxx Trial: Patients who have suffered injuries due to Vioxx have filed litigation against Merck for selling Vioxx even though Merck allegedly was aware of Vioxx's dangerous side effects.