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A product labeled for research use is not the same as a patient-specific prescription plan
Both the Food and Drug Administration (FDA) and the European Medicines Agency are actively monitoring the psychiatric safety of semaglutide and similar medications after post marketing surveillance reports of depression, suicidal thoughts (ideation), and suicidal behavior in patients taking the drugs for the management of type 2 diabetes or obesity
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Neves JS, Vasques-Nvoa F, Borges-Canha M et al (2023) Risk of adverse events with liraglutide in heart failure with reduced ejection fraction: A post hoc analysis of the FIGHT trial
Rybelsus 3 mg Tablet Summary of Product Characteristics
The idea has pharmacokinetic logic
