The Review
On January 13, 2026, the FDA announced the results of a comprehensive review of 91 studies of GLP-1 receptor agonist peptides covering 107,910 patients.
The review didn't find an increased risk of suicidal ideation or behavior. The agency asked manufacturers to remove the warning from the labels of Saxenda, Wegovy, and Zepbound.
The Backup Data
The review followed earlier reports that came in once the peptides were on the market, the same reports that had prompted the warning in the first place.
The cardiovascular study of semaglutide (SELECT, about 17,600 people) also reported no increase in psychiatric side effects.
What this means
References
- 01U.S. Food and Drug Administration Drug Safety Communication, January 13, 2026. SELECT trial: Lincoff et al. 2023, *New England Journal of Medicine* (PMID 37952131).Source line — see article bodyPMID