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It is found that in the clinical follow-up studies of NAFLD patients, compared with the control group, hepatic fat content and ALT levels were not significantly reduced in Lira group and were associated with an increased incidence of gastrointestinal adverse events [118]

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Severe effects including severe abdominal pain, yellowing of skin or eyes, swelling of the face or throat, difficulty breathing, or very rapid heartbeat require immediate emergency care