Finished product reference
Factor Viii / Von Willebrand Factor
Injection, Powder, Lyophilized, for Solution · Parenteral · 1000 IU/1000 IU · 1000 IU
- List code
- 22419
- Pharmacologic class
- Blood coagulation factors; plasma-derived human factor VIII / von Willebrand factor complex
What it is and how it works
Von Willebrand factor mediates platelet adhesion to damaged subendothelium and platelet aggregation, and acts as a carrier that protects factor VIII from premature degradation. Factor VIII is the cofactor of factor IXa in activating factor X. Replacement of both corrects the haemostatic defect in von Willebrand disease and, through factor VIII, in haemophilia A.
Indications
Prevention and treatment of bleeding, including surgical bleeding, in von Willebrand disease when desmopressin is ineffective or contraindicated; treatment and prophylaxis of bleeding in haemophilia A (congenital factor VIII deficiency).
Dosage and administration (summary)
Dosing is individualised by the haemophilia specialist according to the type and severity of deficiency, body weight, bleeding site or surgery, and monitoring of factor VIII and VWF:RCo (ristocetin cofactor) activity; it is given by slow intravenous injection.
Contraindications
Known hypersensitivity to the active substances or excipients.
Warnings and precautions
Hypersensitivity reactions and development of neutralising antibodies (inhibitors) to factor VIII or VWF may occur, and patients should be monitored for inadequate response. Sustained excessive factor VIII levels increase the risk of thrombosis, particularly in patients with known risk factors; plasma-derived products carry a theoretical risk of transmitting infectious agents.
Pregnancy
Use only if clearly indicated; it may be needed to manage von Willebrand disease around delivery.
Storage and supply
Store at 2–8 °C or below 25 °C according to the product information; do not freeze; protect from light.
Source: reference summary prepared from the EU SmPC/EPAR, BNF and WHO Model Formulary. The approved product information in Iran governs.
Other presentations of the same active ingredient
- Injection · Parenteral · 1000 IU/750 IU52057
- Injection, Powder, Lyophilized, for Solution · Parenteral · 1000 IU/1000 IU · 500 IU50130
- Injection, Powder, Lyophilized, for Solution · Parenteral · 250 IU/190 IU53711
- Injection, Powder, Lyophilized, for Solution · Parenteral · 250 IU/600 IU12423
- Injection, Powder, Lyophilized, for Solution · Parenteral · 500 IU/1200 IU9563
- Injection, Powder, Lyophilized, for Solution · Parenteral · 500 IU/500 IU51012
Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.
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