VPRIV RESOURCES
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
A comprehensive guide on how to dose and administer VPRIV
Key codes and services for billing to healthcare providers
Summary of information for safe and effective use of VPRIV
Overview of Wayne's symptoms, diagnosis journey, and treatment plan
Overview of Roxanne's symptoms, diagnosis journey, and treatment plan
Overview of Laura's symptoms, diagnosis journey, and treatment plan
FOR YOUR PATIENTS
Fill in the VPRIV Start Form via the portal to initiate your patient’s treatment with VPRIV
Download and complete the VPRIV Start Form to initiate your patient’s treatment with VPRIV
Complete this form for your patients to expedite their infusion preparation at their site of care
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.
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.
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.
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.
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.
Connect your patients with this organization so they can find genetic counseling in their area for inherited conditions like Gaucher disease.
