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G., Sanacora, G., Duman, R
In the ELIXA CVOT, lixisenatide was found to be non-inferior to standard of care plus placebo in terms of risk of the composite endpoint (cardiovascular death, myocardial infarction, stroke, or hospitalization for unstable angina)13.4% in the lixisenatide group and 13.2% in the placebo group (hazard ratio, 1.02
Concurrent medications : Your provider reviews other glucose-lowering medications, particularly insulin or sulfonylureas, which may require dose reduction when initiating GLP-1 therapy to prevent hypoglycemia
Weight loss steady Month 5 (8mg): Additional 7-10 lbs
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