What does research say about GLP-1 drugs and NAION?
FDA listed a “potential signal of a serious risk” of NAION for GLP-1 drugs like Ozempic. FDA says it “is evaluating the need for regulatory action” on it. A listing does not mean FDA found that the drugs cause NAION.
The listing was in FDA’s report for late 2024 and covered the whole group of GLP-1 drugs, such as Ozempic and Wegovy. FDA gave that status as of March 6, 2025. FDA says these signals are based wholly or in part on reports in its adverse event system. We did not find a later FDA update on it.
The Ozempic label revised in May 2026 does not warn about NAION, and FDA’s label database found no Ozempic label that mentions optic neuropathy. Its eye warning is about problems from diabetic eye disease.
We found no court ruling that GLP-1 drugs cause NAION. The court has set early steps on that question. Requests to keep out expert opinions, and requests to decide the cases without a trial, are due by July 2, 2027.