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demonstrate that the addition of a long-acting GIPR agonist (LY3537021) significantly reduced the total number of GI AEs induced with liraglutide treatment by 16% and numerically reduced nausea by 15% and vomiting by 3%, but not diarrhea (65)

The SUSTAIN-6 trial for semaglutide (3,297 patients, median 2.1 years), LEADER trial for liraglutide (9,340 patients, median 3.8 years), and REWIND trial for dulaglutide (9,901 patients, median 5.4 years) all included comprehensive adverse event monitoring

reduce the damage caused by oxidative stress by decreasing the expression of oxidants and increasing the level of antioxidants

The Journal of Neuropsychiatry and Clinical Neurosciences

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