Helixate Fs (antihemophilic factor (FVIII) recombinant,full length)
Last reviewed · Source: First Databank (FDB) drug data
Overview
Antihemophilic factor (recombinant) is a biosynthetic (recombinant DNA origin) preparation of antihemophilic factor (blood coagulation factor VIII). The drug is structurally similar to endogenous human factor VIII and produces the same biologic effects as plasma-derived antihemophilic factor (human).
USES: This medication is used to control and prevent bleeding episodes in people with low levels of factor VIII (hemophilia A). It is also used in these patients before surgery to prevent bleeding. People with low factor VIII levels are at risk for bleeding longer after an injury/surgery and for bleeding inside the body (especially into the joints and muscles).
This product contains a man-made form of factor VIII, also called antihemophilic factor. This product is used to temporarily replace the missing factor VIII, a protein (clotting factor) that is normally in the blood, so that the blood can clot and the bleeding can stop. This medication should not be used to treat von Willebrand disease.
Generic name: antihemophilic factor (FVIII) recombinant,full length
Pronunciation: (AN-tye-HEE-moe-FIL-ik FAK-tor, ree-KOM-bi-nant)
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Helixate Fs
Indications
The following indications are listed for Helixate Fs:
- Bleeding Episode In Hemophilia A
- Bleeding Prevention In Hereditary Factor Viii Deficiency
- Hemophilia A
Also known as: Bleeding Prevention In Classic Hemophilia, Bleeding Prevention In Congenital Factor Viii Deficiency, Bleeding Prevention In Hemophilia A, Bleeding Prophylaxis In Hemophilia A, Congenital Factor Viii Deficiency Disease, Hemorrhage Prophylaxis In Hemophilia A, Hemorrhaging In Hemophilia A, Prevention Of Bleeding Episode In Hemophilia A.
Dosing
Dosage of antihemophilic factor (recombinant) is expressed in terms of international units (IU, units) of antihemophilic factor activity; 1 unit is approximately equal to the quantity of antihemophilic factor present in 1 mL of fresh pooled human plasma. In general, administration of 1 unit/kg of antihemophilic factor (recombinant) will increase the circulating factor VIII level by approximately 2 units/dL (2%).
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Drug interactions
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There are no contraindication interactions for this drug.
There are no severe interactions for this drug.
There are no moderate interactions for this drug.
Contraindications
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There are no contraindication contraindications for this drug.
There are no severe contraindications for this drug.
There are no moderate contraindications for this drug.
Adverse reactions
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There are no severe adverse reactions for this drug.
There are no less severe adverse reactions for this drug.
Precautions
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Animal reproduction studies have not been performed to date with antihemophilic factor (recombinant). It is not known whether antihemophilic factor (recombinant) can cause fetal harm when administered to pregnant women, and the drug should be used during pregnancy only when clearly needed.
It is not known whether antihemophilic factor (recombinant) is distributed into human milk. Because many drugs are distributed into milk, caution should be exercised when antihemophilic factor (recombinant) is used in nursing women. Some manufacturers state that the drug should be used in nursing women only if clinically indicated.
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ICD codes
No ICD codes are available for this drug.
Formulary status
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Last reviewed · Source: First Databank (FDB) drug data
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