REGULATORY

G-CSF Preparations under PMDA Review for Anaphylaxis

August 22, 2016

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The Pharmaceuticals and Medical Devices Agency (PMDA) is reviewing the risk of anaphylaxis for G-CSF preparations including Gran (filgrastim) and its biosimilar versions - a move that is likely to result in label changes. Other G-CSF preparations under review are…

To read the full story

G-CSF Preparations Ordered to Add Anaphylaxis in ADR List
September 14, 2016

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