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In both groups, the prevalence of newly reported smell or taste disturbances was tiny, the researchers found, but those taking a GLP-1 were still 48% more likely to develop them

The FDAs declaratory order does not restrict compounders operating pursuant to Section 503A or 503B of the FDCA from compounding semaglutide injection products that are not essentially a copy of an FDA-approved drug and compounded to meet individual patient needs (e.g., different dose or inactive ingredients)

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