In the US, Eculizumab (eculizumab systemic) is a member of the drug class selective immunosuppressants and is used to treat Hemolytic Uremic Syndrome, Myasthenia Gravis, Neuromyelitis Optica and Paroxysmal Nocturnal Hemoglobinuria.
ATC (Anatomical Therapeutic Chemical Classification)
CAS registry number (Chemical Abstracts Service)
Reduction in haemolysis
Immunoglobulin, anit-(human complement C5 α-chain) (human-mouse monoclonal 5G1.1 heavy chain), disulfide wit human-mouse monoclonal 5G1.1 light chain, dimer (WHO)
- Eculizumabum (Latin)
- Eculizumab (German)
- Eculizumab (French)
- Eculizumab (Spanish)
- Eculizumab (OS: USAN, BAN)
- Eculizumab (Genetical Recombination) (OS: JAN)
- AX-451 (IS)
- h5G1.1 (IS)
- h5G1.1VHC+h51.1VLC (IS)
Alexion, Canada; Alexion, Finland; Alexion, Israel; Alexion, Lithuania; Alexion, Norway; Alexion, Poland; Alexion, United States; Alexion Europe, Belgium; Alexion Europe, Netherlands; Alexion Europe, Slovenia; Alexion Europe SAS, Latvia; Alexion Pharma, Ireland; Alexion Pharma, Japan; Alexion Pharma, Sweden; Alexion Pharma Italy, Italy; Alexion Pharma Nordics, Denmark; Alexion Pharma Spain, Spain; Alexion Pharmaceuticals, Australia; Alexion Pharmaceuticals UK, United Kingdom; Lonza, Estonia; Patheon, Russian Federation
- Soliris 300mg
Alexion, Switzerland; Alexion, Luxembourg; Alexion Europe, Austria; Alexion Pharma Germany, Germany
|BAN||British Approved Name|
|JAN||Japanese Accepted Name|
|Rec.INN||Recommended International Nonproprietary Name (World Health Organization)|
|USAN||United States Adopted Name|
|WHO||World Health Organization|
Further information on drug naming conventions: International Nonproprietary Names.
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