Resources and Tools

Take advantage of the wide variety of resources that CSL Behring offers. Order educational materials about von Willebrand disease (VWD), access MySource CSL on bleeding disorders, or register for e-mail updates — and receive a book about VWD with our compliments.

Doctor Discussion Guide
This printable discussion guide can serve as a conversation starter as you and your healthcare provider discuss VWD and treatment with Humate-P.

Patient Education Materials
Find educational materials that can help you manage VWD, such as a list of physical activities you can safely enjoy, and a journal for women with VWD.

Patient Assistance Program
This program provides medically necessary therapies to qualified patients who are uninsured or underinsured, and cannot afford their prescribed therapy.

Reimbursement Resource Center
CSL Behring provides a range of reimbursement services, including individual claims processing reviews, assistance in appeals, insurance investigations into product coverage, and prior approvals for therapies authorization. To speak with a representative, call the Reimbursement Answerline at 1-800-676-4266 Monday through Friday from 8 a.m. to 5 p.m. ET.

MySource CSL
Access a Web site dedicated to increasing awareness about bleeding disorders, including von Willebrand Disease (VWD).

Mix2Vial is a plastic, needle-free transfer device for use with Humate-P. For healthcare providers and parents, the Mix2Vial is efficient and convenient, helping to minimize the risk of accidental injury and the time required to prepare Humate-P.


To stay informed about the latest news in bleeding disorders, you may be interested in attending the conferences and meetings listed below.* CSL Behring will be participating in all of these events, so please stop by our exhibit booth and get information on Humate-P, speak with a CSL Behring representative, or obtain brochures.

Hemophilia Federation of America (HFA)
HFA Symposium

Hemostasis and Thrombosis Research Society (HTRS)
Thrombosis & Hemostasis Summit of North America

International Society of Thrombosis and Haemostasis (ISTH)
Annual SSC Meeting

National Hemophilia Foundation (NHF)
Annual Meeting

American Society of Hematology (ASH)
ASH Annual Meeting and Exposition

Most local hemophilia chapters have a Web site, which typically includes a calendar of events. To find a chapter near you, visit the National Hemophilia Foundation Web site.

Important Safety Information

Antihemophilic Factor/von Willebrand Factor Complex (Human), Humate-P® is approved to treat and prevent bleeding in adult patients with hemophilia A (classical hemophilia). Humate-P also treats spontaneous or trauma-induced bleeding episodes in adults and children with von Willebrand disease (VWD) and prevents excessive bleeding during and after surgery in patients with mild, moderate or severe VWD. Humate-P is not known to prevent spontaneous bleeding episodes.

Do not take Humate-P if you have had extreme sensitivity or an allergic response to antihemophilic or von Willebrand factor preparations. Your doctor will monitor you for events related to abnormal blood clotting.

Humate-P is made from human blood and could contain infectious agents. The risk that these agents may transmit disease cannot be completely eliminated, but has been reduced by screening plasma donors and testing donated plasma for certain viruses, and by inactivating and/or removing viruses during manufacturing.

In studies, more than 5% of patients reported the following adverse reactions to Humate-P: allergic/anaphylactic reactions, including hives, chest tightness, rash, itching, and swelling. The most common adverse reactions after surgery were bleeding at the wound or infusion site, and nosebleeds.

Please see full prescribing information.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit or call 1-800-FDA-1088.

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© CSL Behring 2019. The product information on this site is intended for US residents only. HUM / 10-11-0010(1) 8/2015