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VPRIV RESOURCES
FOR YOU AND YOUR PATIENTS
![Male Doctor with patient](/images/Resources/Nurse and Patient.png)
FOR YOU
Summary of VPRIV, an ERT for type 1 Gaucher disease
Hypothetical patient profiles across VPRIV’s patient population
A quick guide on how to dose and administer VPRIV
![VPRIV Dosing and Infusion Guide](/images/Resources/VPRIV Dosing and Infusion Guide.png)
A comprehensive guide on how to dose and administer VPRIV
![VPRIV Reimbursment coding guide](/images/Resources/VPRIV Reimbursment Flyer.png)
Key codes and services for billing to healthcare providers
![Vpriv Prescribing Information](/images/Resources/Vpriv_PI.png)
Summary of information for safe and effective use of VPRIV
FOR YOUR PATIENTS
![VPRIV Start Form](/images/Resources/VPRIV English Start Form.png)
Fill in the VPRIV Start Form with your patients to initiate treatment with VPRIV
![PreppedAhead Sign Up Form](/images/Resources/PreppedAhead Kit-v2.png)
Give your eligible patients this form to fill in to expedite their infusion preparation at their site of care
![VPRIV Patient Brochure](/images/Resources/VPRIV_patient_brochure_digital.png)
Provide your patients with an overview on type 1 Gaucher disease, how VPRIV can help, and the product support services offered
SOURCES OF INFORMATION AND SUPPORT
There are many rare disease support groups and advocacy organizations that may serve as a source of information and support for patients with Gaucher disease.
![Gaucher Community Alliance (GCA) Logo](/images/Resources/Gaucher Community Alliance.png)
This organization provides emotional support, information, and patient and family resources for anyone affected by Gaucher disease. Your patients can network with others affected by Gaucher disease through this organization.
![National Organization For Rare Disorders (NORD) Logo](/images/Resources/NORD.png)
This organization provides information about rare diseases like Gaucher, but also has more specific functions that may be useful for both patients and HCPs. These include referrals to patient organizations, information about research grants and fellowships, advocacy and medication assistance programs, and networked peer-to-peer support for those with Gaucher disease.
![National Gaucher Foundation Logo](/images/Resources/NGF.png)
Find information on the latest Gaucher disease research, get financial assistance, discuss legislative issues, and find outreach programs. Also participate in live web-based meetings, national conferences, and patient meetings.
![Jewish Genetic Disease Consortium Logo](/images/Resources/JGDC.png)
This group gives your patients access to information about diseases like Gaucher that have a high incidence among those of Ashkenazi Jewish descent. Contact them to connect with relevant organizations.
![National Society of Genetic Counselors Logo](/images/Resources/National Society of enetic Counselor.png)
Connect your patients with this organization so they can find genetic counseling in their area for inherited conditions like Gaucher disease.
IMPORTANT SAFETY INFORMATION
Hypersensitivity reactions, including anaphylaxis, have occurred. The most serious adverse reactions in patients treated with VPRIV were hypersensitivity reactions.
Hypersensitivity reactions were the most commonly observed adverse reactions in patients treated with VPRIV in clinical studies. Patients were not routinely pre-medicated prior to infusion of VPRIV.