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Neuropsychopharmacology 35, 21432154

2 The effect was dose-responsive in these earlier data

Before starting GLP-1 therapy, the team completes medical clearance and baseline labs

Edholm T, Degerblad M, Grybck P, et al

Most cases were mild to moderate, and about 4% of people stopped because of side effects

Context: Thus, the prohibitions set forth in ANVISAs (Brazilian FDA) Rule #67/2007 , which governs Good Manufacturing Practices for Compounding Pharmacies, should also be applicable to these clinics. Decisions to make: timeline to implement vs transition window. Next steps: run a focused gap assessment