PubMed PMID: 28340339
This twice daily injection established the drug class in clinical practice as adjunct therapy for adults not adequately controlled on oral agents
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According to the company's website, it connects patients with US-licensed medical providers and licensed US pharmacies
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In January of this year, the FDA noted that it had "received adverse event reports after patients used compounded semaglutide" and that "patients should not use a compounded drug if an approved drug is available to treat a patient." In July, the agency followed up with a notice that it had "received reports of adverse events, some requiring hospitalization, that may be related to overdoses due to dosing errors associated with compounded semaglutide injectable products." And in August, Eli Lilly, the maker of Zepbound and Mounjaro, sent a series of cease-and-desist letters to providers urging them to stop prescribing compounded versions of those drugs
