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Open communication with your healthcare provider ensures that your overall health is closely monitored and that you receive the necessary care to optimize your well-being while undergoing treatment with semaglutide

This applies to: 503A compounders: Until April 22, 2025 503B facilities: Until May 22, 2025 Important Caveat: The FDA may still take action regarding violations of any other statutory or regulatory requirements, such as to address findings that a product may be of substandard quality or otherwise unsafe

Mentioned below are the scenarios as and when Semaglutide has been contraindicated

Site Reactions: Persistent redness, warmth, or swelling beyond 24 hours post-injection may indicate an allergic reaction or infection

Perioperative management of oral glucose-lowering drugs in the patient with type 2 diabetes