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 Infliximab for Risk of Rhabdomyolysis
The Pharmaceuticals and Medical Devices Agency (PMDA) said on July 18 that Mitsubishi Tanabe’s anti-human TNFα monoclonal antibody Remicade (recombinant infliximab) and its biosimilars have come under review for the potential risk of rhabdomyolysis. Certain safety measures such the revision…
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REGULATORY
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