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[DOI] [PubMed] [Google Scholar] 12.Risk of gastrointestinal adverse events associated with glucagon-like peptide-1 receptor agonists for weight loss

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FDAs Declaratory Order : FDAs 12-page order describes the process that FDA undertook to come to this conclusion and explains that FDA obtained information both from the manufacturer (Eli Lilly) as well as relevant information from from patients, health care providers, and others, including compounders, along with data from other sources that we independently identified. FDA acknowledges several times in the order that: [E]ven when a shortage is considered resolved, patients and prescribers may still see intermittent localized supply disruptions as products move through the supply chain from the manufacturer and distributors to local pharmacies

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