Coagadex (coagulation factor X)
Factor X Intravenous Vial (Ea)
Last reviewed · Source: First Databank (FDB) drug data
Overview
Factor X (human) is a preparation of blood coagulation factor X derived from pooled human plasma.
Factor X (human) is a sterile, purified, lyophilized concentrate of factor X derived from pooled human plasma. All plasma used in the manufacture of factor X (human) is obtained from healthy US donors and is screened for hepatitis B surface antigen and antibodies to human immunodeficiency virus-1 (HIV-1), HIV-2, and hepatitis C virus (HCV). Donor plasma also is tested using a nucleic acid assay for HCV, HIV-1, hepatitis A virus (HAV), hepatitis B virus (HBV) and parvovirus B19.
Factor X (human) is isolated from human plasma and purified using a series of viral inactivation/removal steps, including solvent/detergent treatment, nanofiltration, and terminal dry heat treatment. Reconstituted factor X (human) contains not more than 1 unit/mL of factor II and factor IX. In addition, factor X (human) contains no added biological components such as heparin, albumin, or antithrombin.
Factor X (Stuart-Prower factor) is a vitamin K-dependent plasma proenzyme that plays a central role in the blood coagulation cascade as the first enzyme in the common pathway of thrombus formation. Factor X is synthesized in the liver and circulates in plasma as a 2-chain glycoprotein. The primary structure of human factor X is highly homologous to other vitamin K-dependent clotting factors such as factor VII, factor IX, and protein C and shares similar structure-function relationships.
Factor X can be activated by factor IXa (via the intrinsic pathway) or by factor VIIa (via the extrinsic pathway). Factor X is converted from its inactive form to the active form (factor Xa) by cleavage of a 52-residue peptide from the heavy chain. Factor Xa associates with factor Va on a phospholipid surface to form the prothrombinase complex, which activates prothrombin to thrombin in the presence of calcium ions.
Thrombin then acts upon soluble fibrinogen and factor XIII to generate a cross-linked fibrin clot.
The administration of factor X (human) increases plasma levels of factor X and can temporarily correct the coagulation defect in patients with hereditary factor X deficiency. In a pharmacokinetic, efficacy, and safety trial in 16 patients 12-58 years of age with moderate or severe hereditary factor X deficiency, plasma factor X activity level rapidly increased after initial IV administration of factor X (human) 25 units/kg, reaching a peak at 0.5 hours.
Factor X (human) is cleared slowly from plasma with a half-life of approximately 30 hours. Repeat dosing of factor X (human) does not lead to accumulation in the systemic circulation as there was virtually no difference in the pharmacokinetic profiles for factor X (human) at baseline and at least 6 months later in patients receiving an on-demand treatment regimen (25 units/kg per dose) with the drug for hereditary factor X deficiency.
USES: This medication is used to prevent or control bleeding in people with little or no factor X, a condition also known as Stuart-Prower deficiency. This condition may occur due to being passed down through families (inherited). It may also be caused by a lack of vitamin K or by certain medical conditions (such as amyloidosis, liver disease).
Factor X is a clotting factor in the blood that helps bleeding stop normally. People with little or no factor X are at risk for easy bruising, nose or mouth bleeds, heavy menstrual periods (women), bleeding longer after an injury/surgery, or sudden bleeding (such as in the joints, muscles, head, stomach/gut) without a clear cause.
Generic name: coagulation factor X
Pronunciation: (FAK-tor)
Drug class: Factor X
Therapeutic class: Hematological Agents
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Coagadex
Indications
The following indications are listed for Coagadex:
- Hereditary Factor X Deficiency Disease
Also known as: Hereditary Stuart-Prower Deficiency Disease.
Dosing
Dosage of factor X (human) is expressed in international units (IU, units) of factor X activity. Generally, administration of 1 unit/kg of factor X (human) increases plasma factor X levels by 2 units/dL. The activity of factor X (human) in Coagadex(R) (Bio Products Laboratory) is determined using an in vitro chromogenic assay and based on a factor X concentrate reference standard, which is calibrated against the World Health Organization (WHO) 3rd International Standard for Blood Coagulation Factors II and X, Concentrate. The specific activity of factor X (human) in Coagadex(R) is approximately 80-137 units per mg of protein.
No dosing information is available for this tab.
No dosing information is available for this tab.
No dosing information is available for this tab.
Drug interactions
Formal drug interaction studies with factor X (human) are lacking.
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
Factor X (human) is contraindicated in patients who have had life-threatening hypersensitivity reactions to factor X (human) or any component in the formulation.
There are no contraindication contraindications for this drug.
There are no severe contraindications for this drug.
- No disease contraindications
Adverse reactions
Adverse effects reported in at least 5% of patients receiving factor X (human) in clinical trials include infusion site erythema, infusion site pain, fatigue, and back pain.
Less Frequent
- Allergic dermatitis
- Anaphylaxis
- Angioedema
- Dyspnea
- Erythema
- Fibrinogen excess
- Skin rash
- Thrombotic disorder
- Urticaria
Rare or Very Rare
- Acute myocardial infarction
- Cerebrovascular accident
- Chest tightness
- Disseminated intravascular coagulation
- Hemolytic anemia
- Hypersensitivity drug reaction
- Hypertension
- Injection site infection
- Pulmonary thromboembolism
- Thromboembolic disorder
- Wheezing
More Frequent
- Dizziness
- Fever
- Headache disorder
- Injection site sequelae
- Nausea
Less Frequent
- Chest discomfort
- Chills
- Drowsy
- Dyspepsia
- Flushing
- Insomnia
- Lethargy
- Pruritus of skin
- Upper respiratory infection
- Vomiting
Rare or Very Rare
- Acute abdominal pain
- Cough
- Diarrhea
- Dysgeusia
- Fatigue
- Hypotension
- Paresthesia
- Sensation of warmth
- Tachycardia
Precautions
No enhanced messaging available.
Safety and efficacy of factor X (human) have not been established in patients younger than 12 years of age.
There are no adequate and well-controlled studies of factor X (human) in pregnant women. Data from animal reproduction studies performed with factor X (human) are lacking. It is not known whether factor X (human) can affect reproduction capacity or can cause fetal harm when administered to pregnant women. Factor X (human) should be used during pregnancy only when clearly needed.
It is not known whether factor X (human) is distributed into human milk. Because many drugs are distributed into milk, caution should be exercised when factor X (human) is used in nursing women.
The safety and efficacy of factor X (human) in geriatric patients have not been established. As with any patient receiving factor X (human), dosage should be individualized in geriatric patients.
ICD codes
| Code | Type | Description |
|---|---|---|
| Hereditary factor X deficiency disease | ||
| D68.2 | ICD10CM | Hereditary deficiency of other clotting factors |
ICD code information from First Databank (FDB).
Formulary status
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Last reviewed · Source: First Databank (FDB) drug data
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