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PAP also excludes Medicare beneficiaries, and you should verify the current rules at novocare.com/diabetes/help-with-costs/pap.html before relying on it

No dose adjustment is needed based on kidney function

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Still, the FDA said that, Many of the adverse events reported for compounded products appear to be consistent with adverse events related to the FDA-approved versions of these products

Significant weight loss typically becomes apparent over several months as the dose is gradually increased

So the question is: Is there going to be increased pressure on the starting doses of tirzepatide and semaglutide? The restrictions on compounded GLP-1 products come as concerns about existing shortages are bubbling