Sevenfact (coagulation factor VIIa recombinant-jncw)

Factor VII Intravenous Vial (Ea)

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Factor VIIa (recombinant) is a biosynthetic preparation of blood coagulation factor VIIa prepared using recombinant DNA technology.

Factor VIIa (recombinant) is a sterile, lyophilized powder containing biosynthetic blood coagulation factor VIIa prepared using recombinant DNA technology. Factor VIIa (recombinant) is structurally similar to endogenous human factor VIIa and promotes hemostasis through activation of the extrinsic blood coagulation pathway. Factor VIIa is a cofactor in the activation of factor X (Stuart-Prower factor) to factor Xa and factor IX (Christmas factor) to IXa.

Following injury to the vessel wall, tissue factor (TF) is exposed to circulating blood; factor VIIa forms complexes with TF on TF-bearing cells, where these complexes activate factor X to factor Xa and factor IX to factor IXa. Factor Xa, in the presence of activated factor V (labile factor), negatively charged phospholipids, and calcium, converts prothrombin to thrombin and subsequently fibrinogen is converted to fibrin to form a hemostatic plug that provides local hemostasis. This process may also occur on the surface of activated platelets.

Factor VIIa (recombinant) produces hemostasis in the absence of factor VIII or factor IX by binding to activated platelets and directly activating factor X to generate thrombin independently of TF. Administration of factor VIIa (recombinant) increases circulating concentrations of factor VIIa approximately 1000-fold higher than physiologic levels.

Factor VIIa (recombinant) is used for the treatment and prevention of hemorrhagic episodes in patients with hemophilia A (antihemophilic factor (factor VIII) deficiency; classic hemophilia) or hemophilia B (factor IX deficiency; Christmas disease) who have developed inhibitors (alloantibodies) to factor VIII or factor IX, respectively. The drug also is used for the treatment and prevention of hemorrhagic episodes in patients with acquired hemophilia (i.e., those with acquired inhibitors to factor VIII or IX). In addition, factor VIIa (recombinant) is used for the treatment and prevention of hemorrhagic episodes in patients with congenital factor VII deficiency.

Generic name: coagulation factor VIIa recombinant-jncw
Pronunciation: (factor VIIA,ree-KOM-bin-unt)
Drug class: Factor VII
Therapeutic class: Hematological Agents

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Sevenfact:

  • Bleeding Episode In Hemophilia A
  • Bleeding Episode In Hemophilia B

Also known as: Hemorrhaging In Hemophilia A, Hemorrhaging In Hemophilia B.

Dosing

No dosing information is available for this tab.

Drug interactions

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Contraindications

The manufacturer states that there are no known contraindications to the use of factor VIIa (recombinant).

Adverse reactions

The most common adverse effects reported in clinical trials in patients receiving factor VIIa (recombinant) include fever, hemorrhage, hypertension, hypotension, injection site reaction, arthralgia, headache, nausea, vomiting, pain, edema, and rash.

Precautions

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ICD codes

CodeTypeDescription
Bleeding episode in hemophilia A
D66ICD10CMHereditary factor VIII deficiency
Z14.02ICD10CMSymptomatic hemophilia A carrier
Bleeding episode in hemophilia B
D67ICD10CMHereditary factor IX deficiency

ICD code information from First Databank (FDB).

Formulary status

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Last reviewed · Source: First Databank (FDB) drug data