REGULATORY

PMDA Reviewing Osteoporosis Treatment Forteo for Risk of Shock, Anaphylaxis

June 17, 2014
The Pharmaceuticals and Medical Devices Agency (PMDA) announced on June 13 that it is reviewing the risk of shock and anaphylaxis associated with Eli Lilly Japan’s osteoporosis treatment Forteo SC Injection Kit 600 μg (recombinant teriparatide). Certain safety measures including…

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REGULATORY

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