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The microdose program typically starts at a very low dose of 0.2 mg per week , with the ability to adjust up to a maximum of 0.6 mg if needed

Recent office notes showing BMI, A1C lab results, medication trial history, and comorbidity diagnoses

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[13] [14] [15] [16] [17] Adverse events are most commonly gastrointestinal symptoms such as nausea and diarrhea, with relatively low rates of study discontinuation and infrequent serious adverse events reported during trials

Triglyceride levels typically decrease by 25-35%, addressing a key marker for cardiovascular disease risk