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The FDA has documented several concerns specifically involving compounded GLP-1 products: dosing errors (including doses far exceeding the FDA-approved label), improper storage during shipping affecting medication integrity, reports of fraudulent or counterfeit compounded products, adverse event reports associated with compounded GLP-1 use, and the use of semaglutide salt forms (such as semaglutide sodium or semaglutide acetate) that should not be used for compounding