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(More information can be found in Foleys article GLP-1 Drugs: FDA Removes Semaglutide from the Drug Shortage List), The FDA has raised health and safety concerns about these compounded medications, citing issues such as dosing errors, poor inspection records from overseas manufacturers, and, in some instances, adverse events, some of which required medical intervention, These compounded medications are often inaccurately labeled as generic versions of semaglutide and tirzepatide injections and may contain additives, such as vitamins, which have not been approved by the FDA or evaluated through clinical trials, and The FDA has not approved any oral GLP-1 medications, nor has it approved the use of GLP-1 medications for cosmetic purposes

These reports have played a crucial role in prompting regulatory reviews and updates to the warning labels for these medications

How would one little patch placed there impact systemic things like the claims related to improved sleep and wound healing elsewhere

Semaglutide is a GLP-1 receptor agonist that mimics a natural hormone released in the intestine after eating

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Mounjaro commonly causes similar gastrointestinal adverse effects, especially during dose escalation