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Is there a basis to conclude, for each FDA-approved product that includes the nominated bulk drug substance, that: (a) an attribute of the FDA-approved drug product makes it medically unsuitable to treat certain patients for a condition that FDA has identified for evaluation, and (b) the drug product proposed to be compounded is intended to address that attribute

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(In Spanish) [DOI] [PubMed] [Google Scholar] 20.American Society of Anesthesiologists Consensus-Based Guidance on Preoperative Management of Patients (Adults and Children) on Glucagon-like Peptide-1 (GLP-1) Receptor Agonists

The Medicines and Healthcare products Regulatory Agency (MHRA) and manufacturers provide detailed storage instructions in the patient information leaflet supplied with each medication