FDA Calls for Removal of Suicide Warnings from Weight-Loss Drugs

Do GLP-1 drugs reduce suicide risk, or do they increase it by 45% as some international research suggests?
FDA Calls for Removal of Suicide Warnings from Weight-Loss Drugs
Above: A weighing scale in a bathroom in Berlin, Germany on April 1, 2022. Image credit: Annette Riedl/Picture Alliance/Getty Images

The Facts

  • The Food and Drug Administration on Tuesday instructed Eli Lilly and Novo Nordisk to remove warnings about the risk of suicidal thoughts and behavior from the labels of their GLP-1 weight-loss drugs, such as Wegovy, Saxenda, and Zepbound.
  • The FDA's comprehensive review found no increased risk of suicidal ideation or behavior associated with the use of GLP-1 drugs. The decision follows more than a year of studies into reported side effects in people taking the injectable medications.
  • At the time of the original FDA approvals, the labeling for the weight-loss products included information about such risks based on reports of events observed with older medicines used or studied. Versions of the drugs approved for diabetes don't carry the warnings.

Sources Split


The Spin


Narrative A

Large-scale research definitively shows GLP-1 drugs like semaglutide pose no increased suicide risk. Studies of over 60,000 patients found those on semaglutide actually reported lower rates of suicidal ideation than patients on other weight-loss medications, with zero suicide attempts versus 14 in comparison groups.

Narrative B

International research reveals that semaglutide carries a 45% higher risk of suicidal ideation compared to other medications, particularly dangerous for patients with anxiety or depression. The 107 reported cases and two completed suicides demand urgent clarification and warrant precautionary warnings on medication labels.


Metaculus Prediction

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© 2026 Improve the News Foundation.

All rights reserved.

Version 7.17.1