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Highly Regulated (List I)

NOVOSEVEN

1MG/FL. DE PDRE. (50KUI/FL. DE PDRE.)/Lyophilised Powder + Solvent for Injectable Sol./EPTACOG ALFA (ACTIVE)
NOVO NORDISK
ManufacturerVerified lab

NOVO NORDISK

Public retail price
N/ADZD

Identification

Active ingredient (INN)
EPTACOG ALFA (ACTIVE)
Internal code
12 J 160
Country of Origin
Denmark
Pharmaceutical form
Lyophilised Powder + Solvent for Injectable Sol.
Prescription List
Highly Regulated (List I)
Packaging
b/1fl. de pdre. + 1fl. de solvt.
NOVOSEVEN
Clinical View
Highly Regulated (List I)

DAWA Clinical Workbench v2.0

Information may not be accurate. Always consult a physician, pharmacist, or specialist before acting on any data shown here.

Description

Recombinant human coagulation Factor

VIIa (rFVIIa), intended for promoting hemostasis by activating the extrinsic pathway of the coagulation cascade.

NovoSeven is a vitamin

K-dependent glycoprotein consisting of 406 amino acid residues.

Cloned and expressed in hamster kidney cells, the protein is catalytically active in a two-chain form.

Indications

For treatment of hemorrhagic complications in hemophilia A and B.

Pharmacodynamics

Used in the treatment of bleeding episodes in hemophilia A or B. NovoSeven is recombinant Factor VIIa and, when complexed with tissue factor can activate coagulation Factor X to Factor Xa, as well as coagulation Factor IX to Factor IXa.

Xa, in complex with other factors, then converts prothrombin to thrombin, which leads to the formation of a hemostatic plug by converting fibrinogen to fibrin and thereby inducing local clotting.

Adverse Effects

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Alternatives