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Boards of pharmacy, drug maker taking action In late April, the FDA recognized that some compounders were substituting untested and unproven salt forms of semaglutide (ie, semaglutide sodium and semaglutide acetate) rather than its base form
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While MS is not a contraindication to semaglutide therapy, careful consideration of the medication's adverse effect profile, potential drug interactions with disease-modifying therapies, and individual patient factors is essential
[1] These effects are typically most pronounced during dose escalation and often diminish over time as the body adjusts to the medication
The difference between 5 units and 7 units represents 0.2 mg of semaglutide, which is nearly a full dose level difference