BUSINESS

Takeda Withdraws European MAA for Anemia Treatment Peginesatide Following Voluntary Recall in US

July 2, 2013
Takeda Pharmaceutical announced on July 1 that its subsidiary withdrew on June 28 its European marketing authorization application (MAA) for the anemia treatment peginesatide, upon reports of serious hypersensitivity reactions including some death in the US. The subsidiary, Takeda Development…

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BUSINESS

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