Intended for US Healthcare Professionals Only

Need for Effective On-Demand Treatment

In von Willebrand disease6,7

People with von Willebrand disease can be susceptible to spontaneous and traumatic bleeding, including:

Nosebleeds
Abnormal Bruising
Gum Bleeds
Joint Bleeds
Gastrointestinal Bleeds
Heavy Menstrual Bleeding
Muscle Bleeds
Heavy bleeding during or after childbirth

The efficacy of wilate®

On-demand treatment of bleeds has been demonstrated in clinical trials in adults and children with all types of von Willebrand disease2

Data from four prospective, Phase II and III trials

Patients by von Willebrand disease type

Type 3
21
70%
Type 2
2
7%
Type 1
7
23%

wilate® efficacy rated ‘excellent’ or ‘good’

of 1095 treated bleeding events

Type of bleeding event*

Joint
52%
Epistaxis
9%
Gastrointestinal
13%
Oral
3%
Heavy Menstrual Bleeding
6%
Other
18%

On-demand treatment of bleeds is supported by data from real-world studies

WIL-20: Non-interventional Phase IV study3

WIL-20 included 111 patients (aged 1 to 83 years) at 31 centers. 29 patients were treated on-demand with wilate®

wilate® efficacy rated ‘excellent’
or ‘good’ in

of 127 treated bleeding events*

*as rated by the investigator

On-demand treatment of bleeds is supported by data from real-world studies

Real-world retrospective studies

wilate® efficacy rated ‘excellent’ or ‘good’

of 46 bleeding events in 25 adults (median age 42 years, range 19–82 years)4

of 44 bleeding events in 15 adolescents and children (median age 7 years, range 0–17 years)5

Indications and Important Safety Information for wilate® [von Willebrand Factor/Coagulation Factor VIII Complex (Human)].

Please see wilate® full Prescribing Information.

Indication

wilate® is a von Willebrand Factor/Coagulation Factor VIII Complex (Human) indicated in adult and pediatric patients with von Willebrand disease for on-demand treatment and control of bleeding episodes; for perioperative management of bleeding; and for routine prophylaxis to reduce the frequency of bleeding episodes. wilate® is also indicated in adult and pediatric patients 12 years of age and older with hemophilia A for on-demand treatment and control of bleeding episodes; and for routine prophylaxis to reduce the frequency of bleeding episodes.

Contraindications

Do not use in patients with known hypersensitivity reactions, including anaphylactic or severe systemic reaction, to human plasma-derived products, any ingredient in the formulation, or components of the container.

Warnings and Precautions

  • Anaphylaxis and severe hypersensitivity reactions are possible
  • Thromboembolic events may occur. Monitor plasma levels of FVIII activity
  • Neutralizing antibodies (inhibitors) to VWF and Factor VIII have occurred following administration of wilate®. Test for neutralizing antibodies if plasma VWF and/or Factor VIII level fail to increase as expected or if bleeding is not controlled after wilate® administration
  • wilate® is made from human plasma and carries the risk of transmitting infectious agents

Adverse Reactions

The most common adverse reactions (≥ 1%) in clinical trials on VWD were hypersensitivity reactions, urticaria, chest discomfort, and dizziness. The most common adverse reaction (≥ 1%) in clinical trials in hemophilia A was pyrexia (fever).

Please see wilate® full Prescribing Information.

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FOR U.S. HEALTHCARE PROFESSIONALS ONLY

The information on this website has been specifically created 
for U.S. healthcare professionals (HCPs)

Please see wilate® full Prescribing Information