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Similarly, sensitivity analysis was performed after excluding patients who took DPP-4 inhibitors and results were consistent (Supplementary Table 2)

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However, Phase 3 trials with thousands of patients are needed to fully characterise the safety profile, including rare adverse events

Severe or persistent vomiting, severe abdominal pain, fainting, dehydration, confusion, or symptoms of low blood sugar need prompt medical assessment, especially after a possible dosing error