The widow of a man who died only days before the FDA announced the Darvon and Darvocet recall has filed a wrongful death lawsuit. According to the lawsuit, the victim was prescribed the medication on July 30, 2010, to manage his pain. He was on the medication until he died, November 2, 2010, from sudden heart problems. The plaintiff alleges that the distributor, Xanodyne Pharmaceuticals, knew or should have known about the serious risks associated with the medications—including the risk of potentially fatal heart rhythm issues—but did not adequately warn doctors and patients about those risks.
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Darvon first appeared on the market in 1957. In 2009, an FDA panel voted 14 to 12 to recommend that Darvon be removed from the market, finding the drug's benefits did not outweigh its risks. At the time, however, the FDA chose to reject the panel's recommendations.
Darvon is known generically as propoxyphene. Darvocet combines propoxyphene with acetaminophen. The recall affects the brand-name and generic versions of the drugs.
A petition has been filed to have all federal Darvon and Darvocet lawsuits be consolidated in a single federal court. Some attorneys suggest that thousands of lawsuits could be filed against companies that manufactured Darvon, Darvocet and their generic counterparts.