For the treatment of VWD


Prescribing Information

The Octapharma wilate Free Trial is a unique opportunity for people with von Willebrand Disease (VWD) and their providers to experience the safety, efficacy and convenience of wilate® von Willebrand Factor/Coagulation Factor VIII Complex (Human) at no cost.
If you are currently using another VWF/FVIII product, or not currently using factor treatment, your physician may want to consider wilate®. With the Octapharma wilate Free Trial, eligible VWD patients can receive treatment with wilate® (up to 5,000 IUs) at no cost, shipped directly to you and administered under the supervision and care of your physician.
There’s never been a better time to try wilate® and see first hand if wilate® is right for you.

How it works…

  • Talk with your healthcare provider about the Octapharma wilate® Free Trial
  • Complete the Enrollment and Patient Consent Forms together with your physician
  • Your physician writes a prescription for wilate®
  • Fax the signed Enrollment and Patient Consent Forms with the prescription to the Program Administrator (Covance at 1-800-554-6744)
  • Program Administrator reviews documents to ensure you meet the program criteria
  • Program Administrator processes the completed Enrollment and Patient Consent Forms and sends the prescription to pharmacy for dispensing of wilate®
  • Program Administrator confirms wilate® is shipped to you
  • wilate® is administered under the supervision and care of your physician






Indications and Usage

wilate® is a von Willebrand Factor/Coagulation Factor VIII Complex (Human) indicated in children and adults with von Willebrand disease for on-demand treatment and control of bleeding episodes, and for perioperative management of bleeding. wilate® is not indicated for the treatment of hemophilia A.

Important Safety Information

wilate® is contraindicated for patients who have known anaphylactic or severe systemic reaction to plasma-derived products, any ingredient in the formulation, or components of the container.

Hypersensitivity or allergic reactions have been observed upon use of wilate® and may in some cases progress to severe anaphylaxis (including shock) with or without fever.

When using a factor VIII (FVIII)-containing von Willebrand Factor (VWF) product, the treating physician should be aware that continued treatment may cause excessive rise in FVIII activity. Monitor plasma levels of VWF:RCo and FVIII activities in patients receiving wilate® to avoid sustained excessive VWF and FVIII activity levels, which may increase the risk of thrombotic events.

Patients with VWD, especially type 3 patients, may potentially develop neutralizing antibodies (inhibitors) to VWF, manifesting as an inadequate clinical response. Since inhibitor antibodies may occur concomitantly with anaphylactic reactions, patients experiencing an anaphylactic reaction should also be evaluated for the presence of inhibitors.

wilate® is made from human plasma. As with all plasma-derived products, the risk of transmission of infectious agents, eg, viruses and, theoretically, the variant Creutzfeldt-Jakob disease (vCJD) agent or other unknown infectious agents, cannot be completely eliminated. Despite measures to reduce this risk, such products may still potentially transmit disease.

The most common adverse reactions to treatment with wilate® in patients with VWD have been urticaria and dizziness. The most serious adverse reactions to treatment with wilate® in patients with VWD have been hypersensitivity reactions.

Please see full prescribing information.

To report suspected adverse reactions, contact:
Octapharma USA Inc.
866-766-4860 or
FDA at 1-800-FDA-1088 or

Photos are of models and for illustrative purposes only.

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