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 New Safety Risks for Brilinta, Stocrin, Ofev
The Pharmaceuticals and Medical Devices Agency (PMDA) is investigating new side effect risks for three APIs including AstraZeneca’s antiplatelet agent Brilinta (ticagrelor), a move likely to trigger label changes in the near future. According to the agency’s risk communication update…
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REGULATORY
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