In the absence of compatibility studies, ULTOMIRIS® 300 mg/30 mL concentrate for solution for infusion must not be mixed with ULTOMIRIS® 300 mg/3 mL or 1,100 mg/11 mL concentrates for solution for infusion.1
Drag the button across the slider bar in order to select your patient's body weight (kg). The body weight variable will automatically snap to the nearest recognised figure in line with the ULTOMIRIS® weight-based dosing.Please report any adverse events via your national reporting system. Adverse events can also be reported to Alexion Pharmaceuticals by contacting: https://contactazmedical.astrazeneca.com/
† SOLIRIS® (eculizumab) is indicated in adults and children for the treatment of Atypical haemolytic uremic syndrome (aHUS).2
‡ ULTOMIRIS® should only be diluted using sodium chloride 9 mg/mL (0.9 %) solution for injection.1
§ Patients must be vaccinated against meningococcal infection 2 weeks prior to initiating treatment. If patients need to initiate ravulizumab treatment less than 2 weeks after receiving a meningococcal vaccine, must receive treatment with appropriate prophylactic antibiotics until 2 weeks after vaccination.1healthcare professional