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 Safety Risk of Imusera/Gilenya
The Pharmaceuticals and Medical Devices Agency (PMDA) is investigating a new side effect risk for the multiple sclerosis (MS) treatment Imusera/Gilenya (fingolimod), a move likely to trigger label changes in the near future. According to the agency’s risk communication update…
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