Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Rivaroxaban Under Review for Risk of Interstitial Pneumonia: PMDA
The Pharmaceuticals and Medical Devices Agency (PMDA) announced risk information on Bayer Yakuhin’s factor Xa inhibitor rivaroxaban (brand name: Xarelto) and multikinase inhibitor regorafenib (Stivarga) on January 24. The information is currently under review and could result in the revision…
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REGULATORY
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