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 Anaphylaxis Risk for Xocova
The Pharmaceuticals and Medical Devices Agency (PMDA) is assessing a new side effect risk of anaphylaxis for Shionogi’s oral COVID-19 treatment Xocova (ensitrelvir).The assessment, which was revealed in the agency’s risk communication update on June 28, is expected to result…
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