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FDA alerts health care providers, compounders and patients of dosing errors associated with compounded injectable semaglutide products What health care providers, compounders and patients should know FDA has received reports of adverse events, some requiring hospitalization, that may be related to overdoses due to dosing errors associated with compounded semaglutide injectable products
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New England Journal of Medicine (2024) This phase 2 dose-finding trial randomized 190 participants with biopsy-confirmed metabolic dysfunction-associated steatohepatitis (MASH) and stage F2 or F3 fibrosis to tirzepatide 5mg, 10mg, or 15mg weekly or placebo for 52 weeks
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Storage at 20C for lyophilized stock and 28C for reconstituted aliquots is the conservative recommendation
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