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Design: This was a multicentre (n = 20), randomised, double-blind, placebo-controlled, parallel-group study

Step 5: Communicate and document Document the medication, dose, last dose, symptoms, risk assessment, shared decision-making, and final perioperative plan

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To report suspected adverse reactions to compounded GLP-1s, contact the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch