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GLP-1 Eye Risk: FDA Orders New Warnings

The FDA orders GLP-1 eye risk warnings for diabetes and weight-loss medicines after reviewing NAION evidence. Read what the changes mean for care.
GLP-1 eye risk warning highlights rare optic nerve condition linked to potential vision loss
Image | Life Collection Photo | Adobe Stock/2238586075

GLP-1 eye risk has prompted the US Food and Drug Administration (FDA) to require new warnings across medicines with GLP-1 receptor activity.

Announced on 9 November, the changes concern non-arteritic anterior ischaemic optic neuropathy (NAION), a rare condition that can cause permanent sight loss. Manufacturers must include the potential increased risk in prescribing information’s warnings and precautions section.

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