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Wilfactin

Active Ingredient:
Human Von Willebrand Factor
Origin:
EU

Wilfactin (Human Von Willebrand Factor)

Wilfactin is a human von Willebrand factor product used to treat von Willebrand disease, a bleeding disorder. It helps control and prevent bleeding episodes by replacing the missing or defective protein. Suitable for patients requiring factor replacement therapy.

Manufacturer / TM Owner

Lfb Biomedicaments

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Indications & Clinical Uses

  • Wilfactin is used to manage and prevent bleeding in individuals with von Willebrand disease, a condition where blood does not clot properly. It provides the missing von Willebrand factor, which is essential for normal blood clotting. This medication is typically used during surgeries, dental procedures, or in response to injury to reduce bleeding risk. It may also be used for long-term prevention in certain cases.

Side Effects

  • After administration, Wilfactin works by increasing levels of von Willebrand factor in the blood, supporting the clotting process. Patients may notice reduced bleeding episodes or improved clotting function over time. The effects vary by individual and depend on the severity of the condition and the dose received.

Precautions & Warnings

  • Wilfactin should be handled with care to avoid contamination. It is typically administered by a healthcare professional in a clinical setting. Patients should inform their doctor of any allergies or previous reactions to blood products. Regular monitoring may be required to assess response and adjust treatment as needed.

Avoid Interactions

  • Wilfactin may interact with other medications that affect blood clotting, such as anticoagulants or antiplatelet drugs. Patients should inform their healthcare provider about all medications they are taking. No specific food or alcohol interactions have been widely reported, but caution is advised with substances that may increase bleeding risk.

Frequently Asked Questions

Wilfactin is used to treat and prevent bleeding in people with von Willebrand disease by replacing the missing von Willebrand factor.

Wilfactin is given as an intravenous infusion by a healthcare professional in a clinical or hospital setting.

Wilfactin is specifically for von Willebrand disease and is not indicated for hemophilia, which involves factor VIII deficiency.

Pregnant women should consult their doctor before using Wilfactin, as safety depends on individual medical circumstances.

Common effects may include headache, nausea, or reactions at the infusion site, but these vary by patient.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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