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<rss version="2.0"><channel><title>US regulator orders makers of weight-loss drugs to carry blindness risk warning — Live Feed</title><link>https://www.live-feeds.com/feed/us-regulator-orders-makers-of-weight-loss-drugs-to-carry-blindness-risk-warning</link><atom:link xmlns:atom="http://www.w3.org/2005/Atom" href="https://www.live-feeds.com/feed/us-regulator-orders-makers-of-weight-loss-drugs-to-carry-blindness-risk-warning/rss.xml" rel="self" type="application/rss+xml"/><description>Continuously updated, source-cited coverage.</description>
<item><title>FDA orders blindness-risk warning for weight-loss drugs Ozempic, Zepbound</title><link>https://www.live-feeds.com/feed/us-regulator-orders-makers-of-weight-loss-drugs-to-carry-blindness-risk-warning</link><guid isPermaLink="false">https://www.live-feeds.com/feed/us-regulator-orders-makers-of-weight-loss-drugs-to-carry-blindness-risk-warning#u197614</guid><pubDate>Thu, 12 Nov 2026 20:39:36 +0000</pubDate><description>The U.S. Food and Drug Administration has mandated that manufacturers of popular GLP-1 weight-loss and diabetes drugs add a warning about a rare eye condition that can cause sudden vision loss. The label change applies to blockbuster medications including Novo Nordisk&amp;#039;s Ozempic and Wegovy and Eli Lilly&amp;#039;s Zepbound and Mounjaro. The condition, non-arteritic anterior ischemic optic neuropathy (NAION), reduces blood flow to the optic nerve and can result in permanent blindness. The FDA determined the risk warrants a warning after reviewing adverse event reports, though the agency maintai</description></item>
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