Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Reviewing Osteoporosis Treatment Forteo for Risk of Shock, Anaphylaxis
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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