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Rigorous screening for disordered eating is recommended before starting these therapies

Calls To Action to Protect American Patients FDA must put a stop to phony personalization. The FDA must make clear that compounders cannot mass produce manipulated GLP-1 drugs under the false pretense of personalization. Simply adding an ingredient to semaglutide or tirzepatide en masse or changing doses or routes of administration for swaths of patients is not personalization, and it does not create a significant difference for anyone

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So, part of the approach to addressing some of these very complicated patients is working in a partnership with them, because we dont have the answers

Once metabolised, these compounds cannot cross the blood-brain barrier and contribute no cognitive effects