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These results may be compared with those of a post hoc analysis of the LEADER trial, which demonstrated similar incidence rates of MACE in the liraglutide vs placebo group in subjects with a relatively low baseline CV risk (defined as isolated CKD, hypertension with left ventricular hypertrophy, New York Heart Association Class II or III heart failure, and left ventricular systolic or diastolic dysfunction) [37]

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The majority of patients who experience side effects after their first injection find that these symptoms are mild, manageable, and improve significantly within the first week as physiological adaptation occurs