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The FDA is not aware of any basis for compounding a drug using semaglutide salts that would meet the requirements of the federal Food, Drug, and Cosmetic (FD&C) Act. Salt forms have not been shown to be safe and effective. The FDA has received adverse event reports after patients used compounded semaglutide

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Neuprex (a derivate of the human bactericidal permeability protein, rBPI23) is used for the treatment of sepsis, and Omiganan against catheter associated infections (administered as a 2% gel) [164, 165]

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