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The researchers focused on a subset of those patients about 1,700 who either had diabetes, were overweight or had obesity, and compared outcomes after 36 months in those who were prescribed semaglutide to those who werent

The Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) is a spontaneous reporting database monitoring the safety of drugs and biologics after their market approval 14

Therefore, the current meta-analysis was conducted to assess the effect of semaglutide on CV outcomes in T2D patients with and CKD, established CVD, or high CVD risk

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Less nausea and vomiting Nausea is a common side effect of GLP-1s, affecting around 10-25% of participants in clinical trials

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