Resources and support
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IPSEN CARES patient support program can help you get access to your BYLVAY® (odevixibat) prescription with the information and support you need.
To learn more about IPSEN CARES:
IPSENCARES.com
(866) 435-5677
Monday-Friday,
8:00 AM – 8:00 PM ET support@ipsencares.com
Downloadable tools you can take with you
Talking to your doctor about Alagille syndrome
Understand the basics of Alagille syndrome and treatment for cholestatic pruritus (itch)
Download guide
Itch Tracker
Track the severity of itch over time and share with your doctor
Download guide
Itch-related sleep tracker
Track the impact of itch on sleep and share with your doctor
Download guide
Patient brochure
Learn about Alagille syndrome and how BYLVAY can reduce the itch
Download guide
Instructions for Use brochure
Read the full BYLVAY Instructions for Use
Download guide
Instructions for Use Demonstration Booklet - Liquids
Read the guidelines for BYLVAY administration with liquids
Download guide
Instructions for Use Demonstration Booklet - Soft Foods
Read the guidelines for BYLVAY administration with soft foods
Download guide
BYLVAY Prescribing Information - Spanish
Read the Spanish version of the BYLVAY Prescribing Information
Download guide
Instructions for Use brochure - Spanish
Read the Spanish version of the full BYLVAY Instructions for Use
Download guide
Helpful videos
How to open BYLVAY Oral Pellets and mix with food
Watch this brief instructional video for a demonstration on how to open BYLVAY Oral Pellets and mix the contents with a small amount of soft food.
How to open BYLVAY Oral Pellets and mix with liquid
Watch this brief instructional video for a demonstration on how to open BYLVAY Oral Pellets and mix the contents with liquid.
Support organizations
Check out these helpful resources for support, advocacy, and information.
The Alagille Syndrome Alliance (ALGSA) is committed to mobilizing resources, facilitating connections, promoting unity, and advocating for a cure to inspire, empower, and enrich the lives of people affected by Alagille syndrome.
The National Organization for Rare Disorders (NORD) is improving the health and well-being of people with rare diseases by driving advances in care, research, and policy.
The mission of the American Liver Foundation (ALF) is to promote education, advocacy, support services, and research for the prevention, treatment, and cure of liver disease.
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