{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T23:21:18Z","timestamp":1791933678821,"version":"4.3.4"},"reference-count":47,"publisher":"American Medical Association (AMA)","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi240740-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have gained use primarily due to their weight-reduction effects, although a regulatory review was undertaken for potential suicidality concern.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240740-5\">\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>To evaluate potential signals for suicidal and self-injurious adverse drug reactions (ADRs) associated with the GLP-1 RAs semaglutide and liraglutide.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240740-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>Disproportionality analysis through the case-control design using the World Health Organization (WHO) global database of suspected ADRs. Participants were clinical patients worldwide experiencing an ADR suspectedly attributable to semaglutide or liraglutide in the database from inception to August 30, 2023. Data were analyzed from September to December 2023.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240740-7\">\n                    <jats:title>Exposure<\/jats:title>\n                    <jats:p>Treatment with semaglutide or liraglutide regardless of indication or treatment duration.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240740-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Reporting odds ratio (ROR) and the bayesian information component (IC) with 95% CIs were calculated as measures of disproportionate reporting of suicidal and self-injurious ADRs associated with semaglutide and liraglutide compared with all other medications. Sensitivity analyses were conducted including patients with coreported use of antidepressants and benzodiazepines and using dapagliflozin, metformin, and orlistat as comparators. A disproportionality signal was considered when the lower limits of the ROR and IC were above 1 and 0, respectively.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240740-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>A total of 107 (median [IQR] age 48 [40-56] years; 59 female patients [55%]) and 162 (median [IQR] age 47 [38-60] years; 100 female patients [61%]) cases of suicidal and\/or self-injurious ADRs were reported between November 2000 and August 2023 with semaglutide and liraglutide, respectively. Significant disproportionality was detected only for semaglutide-associated suicidal ideation (ROR, 1.45; 95% CI, 1.18-1.77; IC, 0.53; 95% CI, 0.19-0.78), which remained significant in patients with coreported use of antidepressants (ROR, 4.45; 95% CI, 2.52-7.86; IC, 1.96; 95% CI, 0.98-2.63) and benzodiazepines (ROR, 4.07; 95% CI, 1.69-9.82; IC, 1.67; 95% CI, 0.11-2.65), when compared with dapagliflozin (ROR, 5.56; 95% CI, 3.23-9.60; IC, 0.70; 95% CI, 0.36-0.95), metformin (ROR, 3.86; 95% CI, 2.91-5.12; IC, 1.20; 95% CI, 0.94-1.53) and orlistat (ROR, 4.24; 95% CI, 2.69-6.69; IC, 0.70; 95% CI, 0.36-0.95).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi240740-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>This study using the WHO database found a signal of semaglutide-associated suicidal ideation, which warrants urgent clarification.<\/jats:p>\n                  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