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FDA mandates increased warnings for epilepsy drugs, stops short of issuing black box
The U.S. FDA has increased label warnings for epilepsy drugs, noting the increased risk of suicidal thoughts and behaviours, after a panel review earlier this year.
The U.S. FDA has issued new labelling guidelines for drugs used in the treatment of epilepsy. The agency has announced that the directive is relevant for all anti-epileptic drugs, including those for treating psychiatric disorders, migraine headaches, and other conditions.
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