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Clinicians who do prescribe AOD-9604 in this age group under a documented informed-consent framework should, at minimum, measure standing height and sitting height every 3 months, track height velocity against population norms, assess Tanner stage at each visit, and obtain fasting IGF-1 and IGFBP-3 levels at baseline and every 3 months [18]
According to the MHRA Summary of Product Characteristics (SmPC), these include: Nausea (very common, affecting more than 1 in 10 patients) Diarrhoea and vomiting (very common) Constipation (common) Abdominal pain and dyspepsia (common) Decreased appetite (very common) Most gastrointestinal side effects are mild to moderate in severity and tend to diminish over time as the body adjusts to treatment
The Training Pathway: Obesity Medicine Board Certification Heres something important that addresses scope of practice concerns directly
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That include drooping or loose skin, jawline, eyes, lips, and dcolletage
