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 Safety Risks for Plaquenil, Relumina
The Pharmaceuticals and Medical Devices Agency (PMDA) is evaluating new side effect risks for Sanofi’s immune modulator Plaquenil (hydroxychloroquine sulfate) and ASKA Pharmaceutical’s uterine fibroid drug Relumina (relugolix), a move likely to trigger label changes in the near future. Plaquenil…
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