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Drug: Ravulizumab
Brand: Ultomiris 300mg/30ml
Manufacturer /
TM Owner
Alexion
Origin: USA

Ultomiris 300mg/30ml Injection

Ultomiris contains Ravulizumab, a monoclonal antibody. It binds precisely to a disease-driving target, blocking harmful signalling or flagging abnormal cells for immune destruction. It is used in the treatment of hereditary angioedema and complement-mediated disorders. It is supplied as an injection (300mg/30ml). Available on prescription, it forms part of modern, guideline-driven care.
Strength: 300mg/30ml
Pack Size: 1s
Storage: 2°C to 8°C
Form: Injection

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Indications & Clinical Uses

  • Ultomiris (ravulizumab) is a monoclonal antibody directed against complement component C5, indicated for treatment of patients with paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS).
  • Ravulizumab is administered intravenously and provides prolonged complement C5 inhibition for prevention of hemolysis and thrombotic microangiopathy.
  • It is particularly valuable for patients intolerant to or inadequately treated by other complement inhibitors.
  • Ultomiris represents a long-acting therapeutic option with extended dosing intervals compared to other C5 inhibitors.

Side Effects

  • Serious and life-threatening infections are the most significant risk, particularly meningococcal infections; Neisseria meningitidis vaccination is mandatory before treatment initiation.
  • Other common infections include respiratory infections and urinary tract infections.
  • Hypertension occurs in approximately 20% of patients.
  • Headache, nausea, and diarrhea are common gastrointestinal effects.
  • Serious adverse reactions include fulminant meningococcemia (even with vaccination), other invasive infections from encapsulated bacteria, and thrombotic microangiopathy progression in some aHUS patients.
  • Infusion reactions may occur with initial infusions.

Precautions & Warnings

  • BOXED WARNING: Serious meningococcal infections including fulminant sepsis are possible even with meningococcal vaccination.
  • Meningococcal vaccination (MenACWY and MenB if available) is REQUIRED at least 2 weeks before Ultomiris initiation; revaccinate per guidelines (typically every 5 years).
  • Monitor closely for signs of infection, fever, headache, or neck stiffness—seek immediate medical evaluation.
  • Pregnancy category C—use only if benefit justifies fetal risk.
  • Monitor complement levels, hemoglobin (PNH), and renal function (aHUS) during treatment.
  • Infection risk remains elevated for months after discontinuation.

Avoid Interactions

  • No major drug interactions documented with Ultomiris.
  • However, other complement inhibitors (eculizumab, pegcetacoplan) should not be used concurrently—overlapping mechanism increases thrombotic risk.
  • Live vaccines are contraindicated during complement inhibition due to infection risk; defer non-urgent immunizations.
  • Tell your healthcare provider about all medications and supplements.
  • Prophylactic antibiotics are often recommended for infection prevention.
  • NSAIDs should be used cautiously due to potential renal effects in aHUS patients.

References

Frequently Asked Questions

Ultomiris (ravulizumab) is an intravenous antibody treatment for paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS). It blocks complement protein C5 to prevent red blood cell destruction and clotting complications. Ultomiris is given by hospital infusion with long-acting protection.

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