Your participation in this registry will help Amicus Therapeutics, Inc. learn valuable health information regarding pregnancies of women who have Fabry disease. The health information learned from this registry will be shared with the U.S. Food and Drug Administration (FDA) and other regulatory agencies and may help other women who have Fabry disease to better understand the impact the disease and its treatments might have on pregnancies and child development.
Information submitted to the registry will be maintained as confidential in accordance with applicable national privacy regulations and other state and local laws related to medical information.
This voluntary registry will enroll women with Fabry disease, who are/were pregnant or who are/were breastfeeding within the first year of their child's birth. Women currently receiving treatment, and women who previously or never received treatment for their Fabry disease may enroll in the registry.
Pregnant and/or breastfeeding patients who have Fabry disease and have been exposed to at least 1 dose of Galafold® (migalastat) during pregnancy and/or breastfeeding.
Pregnant and/or breastfeeding patients who have Fabry disease, who were not exposed to Galafold during pregnancy and/or breastfeeding.
Please click here for Full Prescribing Information, Including Patient Information and Instructions for Use.
Hours of operation: Mon-Fri 8:00 a.m. to 5:00 p.m. Eastern Time
email: fabrypregnancy@ubc.com
Report a PregnancyInformation submitted to the registry will be maintained as confidential in accordance with applicable national privacy regulations and other state and local laws related to medical information.
Note: Your information will not be shared for any other purpose other than for the Pregnancy Coordinating Center to contact you. Please refer to Privacy Policy and Terms of Use within this website.
Information submitted to the registry will be maintained as confidential in accordance with applicable national privacy regulations and other state and local laws related to medical information.
To report Suspected Adverse Reactions, contact Amicus Therapeutics at 1-877-4AMICUS or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.