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Association between semaglutide and Nonarteritic anterior ischemic optic neuropathy: a multinational population-based study
How do Liraglutide and Semaglutide GLP-1 differ
Clinical assessments were conducted every 3 months to evaluate efficacy, measured as percentage of total weight loss (%TWL), excess weight loss (%EWL), changes in BMI, and improvement in comorbidities, as well as tolerance, monitored for adverse effects including gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea) and discontinuation rates
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These results may have limited generalizability due to bias introduced by the studys design, including the treatment setting (ie, a neuroophthalmology clinic) and potential worse baseline health in patients taking semaglutide compared with matched controls
