Vonvendi® support

Throughout your treatment journey

Takeda has a variety of resources to help people living with von Willebrand disease, including information, guidance, and resources regarding treatment. Talk to your healthcare provider about your goals for treatment.

Customer support representative talking on the phone with a VONVENDI® patient.

FREEDOM OF CHOICE

Ask your healthcare provider if you may be eligible to receive trial doses of VONVENDI with or without FVIII. This Free trial program is for new VONVENDI patients only. Participants must receive consultation and approval from a healthcare provider to participate.*

VONVENDI on-demand and surgery treatment with or without recombinant factor VIII (rFVIII) details:

  • VONVENDI is available for 3 doses as a free trial

VONVENDI for prophylaxis in patients with severe Type 3 VWD receiving on-demand therapy details:

  • VONVENDI is available for 8 doses as a free trial

*Other restrictions may apply. See Program Terms & Eligibility in the below link

Download the forms
Freedom of Choice registration form.

PATIENT STARTER KIT

If you are an adult patient new to VONVENDI you may be able to receive a Patient Starter Kit at no cost to you.

Sign up to request a starter kit and receive updates from VONVENDI.

Sign up now
VONVENDI® Patient brochure.

PATIENT BROCHURE

This brochure can help you decide if you should talk to your healthcare provider about using VONVENDI to manage your bleeding episodes. It includes information about VWD, treatment with VONVENDI, and programs from Takeda.

Download the brochure
von Willebrand disease bleed tracker brochure.

A simple way to track bleeds

Tracking your bleeds can help your healthcare provider better understand how VWD is affecting your body. Download our handy bleed tracker to get started today.

Download bleed tracker Descargar registro de sangrados

Ready to talk to your healthcare provider?

Our easy-to-use Discussion Guide, used alongside our bleed tracker, can help you speak to your healthcare provider about finding a treatment that's right for you.

Download the guide
von Willebrand disease discussion guide.

Hematology Support Center

Takeda Hematology Support Center (HSC) is a dedicated team for eligible patients who have been prescribed Takeda hematology products. HSC assists patients affected by bleeding disorders in gaining access to the Takeda medication prescribed by their physician as well as providing educational resources and information on financial assistance options. Call 1-888-229-8379 Monday–Friday | 8:30AM–8:00PM ET

Visit HematologySupport.com

If you have been prescribed VONVENDI, here are a few ways that the HSC can help:

Case managers checklist icon.

Case Managers

Case Managers are a patient's first point of contact. They can assist with CoPay enrollment and will connect patients to other HSC team members if additional information is required.

Copay assistance icon.

CoPay Assistance

For eligible commercially insured Takeda patients, the CoPay assistance program may cover 100% of eligible out-of-pocket expenses related to a patient’s Takeda Hematology treatment for which there is a co-pay, such as deductibles and coinsurances, up to the program maximum.

Patient Access Manager icon.

Patient Access Managers (PAMs)

Our Patient Access Managers are insurance experts who are trained to help address potential access challenges with Takeda prescribed treatment. PAMs can:

  • Provide insurance and access education tools
  • Help answer questions about insurance access and coverage
  • Address complex coverage issues, such as loss or lapse in insurance coverage

Self-Infusion Trainings icon.

Self-Infusion Trainings

If your healthcare provider prescribed VONVENDI, they can sign you up for self-infusion trainings through HSC. A specially trained nurse can teach you to self-infuse at home or virtually. Talk to your healthcare provider to see if self-infusion may be right for you.

Resources and education icon.

Educational Tools and Resources

Insurance education resources are available to help patients understand insurance and the evolving healthcare landscape. Additionally, HSC connects patients and caregivers with community resources and additional tools available for those living with a bleeding disorder. Healthcare Educators are also a part of the HSC team and are fluent in both Spanish and English. They can provide one-on-one education to caregivers and patients on managing their condition.

IMPORTANT NOTICE: Takeda's HSC Co-Pay Assistance Program (the Program) is not valid for prescriptions eligible to be reimbursed, in whole or in part, by Medicaid, Medicare (including Medicare Part D), Tricare, Medigap, VA, DoD, or other federal or state programs (including any medical or state prescription drug assistance programs). No claim for reimbursement of the out-of-pocket expense amount covered by the Program shall be submitted to any third party payer, whether public or private. The Program cannot be combined with any other rebate/coupon, free trial, or similar offer. Copayment assistance under the Program is not transferable. The Program only applies in the United States, including Puerto Rico and other U.S. territories, and does not apply where prohibited by law, taxed, or restricted. This does not constitute health insurance. Void where use is prohibited by your insurance provider. If your insurance situation changes you must notify the Program immediately at 888-229-8379. Coverage of certain administration charges will not apply for patients residing in states where it is prohibited by law. Takeda reserves the right to rescind, revoke, or amend the Program at any time without notice.

Erica, a real VWD patient sitting at a table smiling.

Become a part of our VWiD community

Through VWiD, adults living with VWD can attend events to hear from VONVENDI users and Takeda Senior Clinical Specialists. Contact your local National Hemophilia Foundation chapter for more information.

Find your chapter
Woman wearing a sweater looking at VONVENDI® information on her tablet.
More facts about VWD

Get to know the most common inherited bleeding disorder.741

Learn more
Leslie, a real VWD patient sitting down looking at the horizon.
Real VWD patients

Our patient ambassadors share their stories
of living with VWD.1

See their stories

References

  1. What is von Willebrand disease? Centers for Disease Control and Prevention website. Accessed July 9, 2020. http://www.cdc.gov/ncbddd/vwd/facts.html