<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"><channel><title>FDA orders new warning on GLP-1s over rare eye condition linked to sudden blindness — Live Feed</title><link>https://www.live-feeds.com/feed/fda-orders-new-warning-on-glp-1s-over-rare-eye-condition-linked-to-sudden-blindness</link><atom:link xmlns:atom="http://www.w3.org/2005/Atom" href="https://www.live-feeds.com/feed/fda-orders-new-warning-on-glp-1s-over-rare-eye-condition-linked-to-sudden-blindness/rss.xml" rel="self" type="application/rss+xml"/><description>Continuously updated, source-cited coverage.</description>
<item><title>FDA orders blindness-risk warning on GLP-1 weight-loss drugs</title><link>https://www.live-feeds.com/feed/fda-orders-new-warning-on-glp-1s-over-rare-eye-condition-linked-to-sudden-blindness</link><guid isPermaLink="false">https://www.live-feeds.com/feed/fda-orders-new-warning-on-glp-1s-over-rare-eye-condition-linked-to-sudden-blindness#u197814</guid><pubDate>Thu, 12 Nov 2026 23:22:11 +0000</pubDate><description>The U.S. Food and Drug Administration has directed manufacturers of popular GLP-1 receptor agonists, including Ozempic, Wegovy, Zepbound and Mounjaro, to add a warning about non-arteritic anterior ischemic optic neuropathy (NAION), a rare eye condition that can cause sudden vision loss. The label change follows reports of NAION in patients using these drugs for diabetes and obesity. The agency says a causal link has not been established but the potential risk warrants disclosure. Drugmakers must update prescribing information and patient medication guides.Why it mattersGLP-1 drugs have become </description></item>
</channel></rss>