eculizumab (Soliris)
Jump to navigation
Jump to search
Indications
- paroxysmal nocturnal hemoglobinuria
- hemolytic uremic syndrome (HUS)[1]
- membranoproliferative glomerulonephritis
- Degos-Touraine syndrome
- AChR-Ab + myasthenia gravis
Dosage
- meningococcal vaccination must be administered to all patients at least 2 weeks prior to the 1st dose of eculizumab*
- infusion 600-900 mg diluted to 5 mg/mL over 35 minutes
- every 7 days during induction phase
- every 14 +/- 2 days during maintenance
- 600 mg weekly for 1st 4 weeks
- 900 mg week 5
- 900 mg every 2 weeks thereafter
300 mg single use vials, 30 ml of 10 mg/mL of sterile solution
* ref[2] case of HUS seemed to have much shorter interval between meningococcal vaccination & first dose of eculizumab
Adverse effects
- > 10-20%%
- increased risk of invasive meningococcal disease
Mechanism of action
- reduces hemolysis by inhibiting terminal complement activation
- targets complement C5
More general terms
References
- ↑ 1.0 1.1 Deprecated Reference
- ↑ 2.0 2.1 Kao AY, Sagar P, Klig JE et al Case 19-2018: A 15-Year-Old Girl with Acute Kidney Injury. N Engl J Med 2018; 378:2421-2429. June 21, 2018 PMID: https://www.ncbi.nlm.nih.gov/pubmed/29924949 https://www.nejm.org/doi/full/10.1056/NEJMcpc1802827
- ↑ http://www.soliris.net/
- ↑ Prescribing Information http://www.soliris.net/sites/default/files/assets/soliris_pi.pdf
- ↑ Medscape: eculizumab (Rx) https://reference.medscape.com/drug/soliris-eculizumab-342875