The European Medicines Agency found no link between semaglutide use and suicidal thoughts or actions, concluding a monthslong probe that followed an inquiry by the FDA that led to a similar conclusion last year.
The EMA’s Pharmacovigilance Risk Assessment Committee (PRAC) began looking last July into reports of patients taking GLP-1s experiencing suicidal thoughts. After examining several studies based on patient health records, the group concluded that there was no need for the manufacturers to take action on their safety labeling.
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