According to some reports, one thousand Actos bladder cancer lawsuits have now been filed in federal court in Louisiana. Some of the lawsuits are wrongful death claims, alleging patients died of bladder cancer after taking Actos. Others are personal injury claims, alleging Takeda Pharmaceuticals and Eli Lilly (who launched the drug together) did not adequately warn patients or medical professionals about the risks associated with the drug.
Plaintiffs allege Actos, a type 2 diabetes drug, was unreasonably dangerous and defective and further claim that Takeda knew about the risk of bladder cancer in patients who used Actos but failed to warn plaintiffs and the medical community about that risk.
Actos wrongful death and personal injury lawsuits filed in federal districts have been transferred to Actos multi-district litigation (In Re: Actos (pioglitazone) Products Liability Litigation, 6:11-md-2299). Actos is still available for use in the US but has had sales suspended in France and Germany, following a study that linked the use of Actos for more than a year with an increased risk of bladder cancer.
READ MORE ACTOS SIDE EFFECTS LEGAL NEWS
News of the generic version of Actos being approved resulted in Consumer Reports issuing a warning about the medication. In Consumer News (8/21/12), the organization warned, "Pioglitzaone can cause serious side effects, such as an increased risk of heart failure, bone fractures, and bladder cancer. Other medications to treat diabetes, such as metformin, are a better first choice."