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Novo Nordisk) it is prescribed to patients for weight management if they have a BMI of 30 or more, or a BMI of 27 or more and at least one weight-related co-morbidity

The FDA has received over 520 adverse event reports tied to compounded semaglutide, and a staggering number of those cases trace back to one root cause: dosing errors

But it's not a green light

What happens if the FDA finalizes its proposal to restrict compounded GLP-1s

9 These trials demonstrated significant weight loss with semaglutide compared to placebo in adults with obesity

Section 503A pharmacies had until April 2025, and Section 503B facilities had until May 2025 to comply