Nebenwirkungen · Ultomiris
Ultomiris 300 mg/3 mL concentrate for solution for infusion Ultomiris 1 100 mg/11 mL concentrate for solution for infusion · Abschnitt 4.8 · PDF-Seite 12
HOS-143205 · Präparat HOS-098946
Atypical haemolytic uremic syndrome (aHUS) In paediatric patients with evidence of aHUS (N= 34, aged 10 months to less than 18 years) included in ALXN1210-aHUS-312 study, the safety profile of ravulizumab appeared similar to that observed in adult patients with evidence of aHUS. The safety profiles in the different paediatric subsets of age appear similar. The safety data for patient below 2 years of age is limited to four patients. The most common adverse reactions (> 20%) reported in paediatric patients were pyrexia, vomiting, diarrhoea, headache, nasopharyngitis, upper respiratory tract infection and abdominal pain.
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