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EMA Asks Takeda to Revise Package Inserts for Pioglitazone Medicines Due to Risk of Bladder Cancer

August 1, 2011
The European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) issued a recommendation on July 21 asking Takeda Pharmaceutical to revise package inserts for the diabetes 2 treatment Actos (pioglitazone) and other products containing pioglitazone to state…

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