Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Patient Dies due to Mix-Up of Lixiana, Rifxima; PMDA, Companies Issue Warning Statement
The Pharmaceuticals and Medical Devices Agency (PMDA) issued a warning statement on its website on October 25 regarding the death of a patient who received Daiichi Sankyo’s oral anticoagulant Lixiana (edoxaban) instead of ASKA Pharmaceutical’s oral antibiotic Rifxima (rifaximin) due…
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REGULATORY
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