fda warning letters compounded semaglutide 2025 september The U.S. Food and Drug Administration (FDA) has issued a to Novo Nordisk over its alleged failure to report adverse side effects, including death, in patients who took its GLP-1 medications FDA sends warning letter after

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9 The semaglutide group exhibited significant improvements in symptoms and physical limitations, assessed using the Kansas City Cardiomyopathy Questionnaire Clinical Summary Score (KCCQ-CSS), with the change in KCCQ-CSS being the primary trial endpoint

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"The possibility of offering new hope to individuals struggling with addiction is what makes this work so meaningful." Source: Journal reference: Quddos, F., et al