Helpful Resources
Published Data
New data was published this month in the Journal of the American Academy of Dermatology showing results from an institutional review board-approved survey comparing the propensity for dispensing and dosing calculation errors of HEMANGEOL (propranolol hydrochloride oral solution 4.28 mg/mL) versus generic propranolol hydrochloride oral solutions (4 mg/mL and 8 mg/mL) during the treatment of infantile hemangiomas. The survey of 220 pediatric dermatologists and other physicians who treat infantile hemangioma found that medication dispensing and calculation errors are very common among physicians prescribing generic propranolol vs. HEMANGEOL.
Click here to see our press release.
Patient Education Materials
HEMANGEOL Dosing Chart
You can use this chart as a tool to instruct parents and caregivers on the proper dosing of HEMANGEOL.
HEMANGEOL Instructions for Use
Parents and caregivers can follow these simple instructions to learn how to properly administer HEMANGEOL.
HEMANGEOL Patient Brochure
This brochure can answer common questions that parents and caregivers may have about infantile hemangioma and HEMANGEOL.
HEMANGEOL Prescribing Information
View this document for more information on HEMANGEOL, including indications and usage, dosage and administration, contraindications, as well as warnings and precautions.
Other Resources
Request a visit
If you would like additional information about HEMANGEOL, our dedicated representatives are available to answer your questions and provide you with the resources you need to educate parents and caregivers.
Find Support for Your Patients and Their Loved Ones
There are a number of advocacy groups dedicated to providing education and support to parents and caregivers of infantile hemangioma patients.
Video resources
Find videos about HEMANGEOL.
Request a Visit
If you are a healthcare professional in the United States and would like a HEMANGEOL representative to contact you, please complete the form below.
Caregiver Support and Patient Advocacy Groups
When a baby first develops an infantile hemangioma, parents and caregivers may experience feelings of confusion, anxiousness, and guilt.
Below is a list of organizations dedicated to providing education and support to all those affected by infantile hemangiomas.
National Organization of Vascular Anomalies (NOVA)
P.O. Box 38216
Greensboro, NC 27438-8216
Website: novanews
The National Organization of Vascular Anomalies is a patient support, advocacy, and educational agency for those affected by infantile hemangiomas, vascular malformations, rare benign tumors, and other related syndromes.
The Vascular Birthmarks Foundation (VBF)
P.O. Box 106
Latham, NY 12110-0106
Phone: (877) 823-4646
Website: birthmark
The Vascular Birthmarks Foundation is an international charitable organization that connects families affected by vascular birthmarks, tumors, or syndromes to the appropriate medical professionals. The foundation also provides informational resources, sponsors physician education, facilitates medical mission trips, and supports research and programs that promote acceptance for individuals with birthmarks.
Video Resources
Early Diagnosis and Treatment of Infantile Hemangioma: The New Paradigm of Care
In this talk entitled “Early Diagnosis and Treatment of Infantile Hemangioma: The New Paradigm of Care,” professors and pediatric dermatologists Ilona Frieden, Sheila Friedlander, and Elaine Siegfried offer information on how to identify, diagnose infantile hemangioma, and treatment options.
Parents share their experience with infantile hemangioma. After discovering a hemangioma on their daughter’s arm, the parents sought help from Dr. Ana Duarte, who provides insight to an available treatment option.