Abstract
The below is from a January 11 Drug Safety Communication from the U.S. Food and Drug Administration (FDA) evaluating reports of suicidal thoughts or actions in patients treated with a class of medicines called glucagon‐like peptide‐1 receptor agonists (GLP‐1 RAs). The initial evaluation found that there is no evidence of a link between these medicines and suicidality. Below is the FDA's report.
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