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The groups that started at 4 mg experienced significantly more nausea, vomiting, and diarrhea than those who began at 2 mg

The Medicines and Healthcare products Regulatory Agency (MHRA) has approved both medications for use in type 2 diabetes, and prescribing information for each drug acknowledges their potential use alongside other glucose-lowering therapies

Our goal is to strike the right balance between effectiveness and tolerability, prioritizing long-term outcomes over quick escalation

These two resources are complementary, not competing

Drug-target MR analysis was used to evaluate the impact of GLP-1RAs on SA, and a two-step MR analysis was further employed to explore potential mediating factors in the T2D-SA relationship