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While the FDA itself has voiced concerns about compounded versions of FDA-approved GLP-1 therapies, the agency is allowing a grace period before taking enforcement action against state-licensed pharmacists/physicians compounding under section 503A (60 days) and outsourcing facilities under section 503B (90 days)

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Whether used for individual prescriptions or specialty program shipments, they deliver the precision GLP-1 therapies demandwithout the environmental footprint of traditional packaging

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Still, patients with type 2 diabetes have reported tiredness after trials, and social media analyses of GLP-1 medications often surface complaints about low energy and sleep disruption