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European Medicines Agency Investigation On January 17, 2025, the European Medicines Agency (EMA) Pharmacovigilance Risk Assessment Committee launched a review of semaglutide medications such as Ozempic and Wegovy due to the increased risk of developing NAION

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Fewer than 10% report persistent bothersome side effects beyond week four, and these cases usually respond well to dose timing adjustments or dietary modifications

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Regulatory status varies by formulation and manufacturing source