Common adverse effects include gastrointestinal symptoms (nausea, vomiting, diarrhea), which can lead to dehydration and electrolyte imbalances
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This pharmacovigilance system is crucial for detecting rare or delayed adverse effects that may not have been apparent in clinical trials
[1] [9] Although the primary endpoints focused on body weight reduction, secondary analyses provided data on hepatic fat content, measured using magnetic resonance imaging-proton density fat fraction (MRI-PDFF) a validated, reference-standard non-invasive technique for quantifying liver fat
La dosis inicial suele ser de 2.5 mg , que se incrementa de manera gradual hasta llegar a 15 mg por semana, dependiendo de la tolerancia del paciente y los resultados obtenidos