The FDA said it is requiring GLP-1 drugs to add information warning about rare risk of vision loss.
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The US Food and Drug Administration ‌on Monday informed patients and healthcare providers of a potential increased risk of a serious eye condition associated with the use of GLP-1 drugs for weight loss and diabetes.

The FDA said it is requiring GLP-1 drugs such ​as Eli Lilly’s Mounjaro and Zepbound, and Novo Nordisk’s Ozempic and Wegovy to add information ​to the “warnings and precautions” section of labeling about the potential increased risk of non-arteritic ⁠anterior ischemic optic neuropathy (NAION).