Patient Frequently Asked Questions

How do I know if I am eligible to participate in the Registry?

You are eligible to participate in the registry if you:

  • were exposed to at least one dose of Mylan-Fingolimod at any time during pregnancy
  • are willing to provide written informed consent and an authorization to release medical information about you and your baby

Who do I contact if I have a question or a concern about participating in the Registry?

Contact your Mylan-Fingolimod prescribing healthcare provider or the Mylan-Fingolimod Pregnancy Registry directly by calling 1-888-246-5830, sending a fax to 1-833-677-0484 or sending an e-mail to

What is an adverse event (AE) and how do I report an adverse event?

An adverse event consists of any unfavorable medical occurrence in the patient enrolled in the study, whether or not expected. If you need to report an adverse event, please contact your healthcare provider or call 1-844-596-9526.

Is compensation provided for participants?

No, registry participants are not provided compensation.

How do I update my contact information?

Contact the Mylan-Fingolimod Pregnancy Registry by calling 1-888-246-5830, sending a fax to 1-833-677-0484 or sending an e-mail to If you are not able to contact the Mylan-Fingolimod Pregnancy Registry. Please advise your healthcare provider.

I am a participant in the Mylan-Fingolimod Pregnancy Registry, but I’ve recently moved address. Can I still participate?

Yes, you can still participate. Please inform your healthcare provider of your move ASAP. If your healthcare professional also changes due to the move, please also provide their contact details to the Mylan-Fingolimod Pregnancy Registry. We will contact your new healthcare provider, to follow-up on your participation into the registry.

Where do I find more information about Mylan-Fingolimod?

Please visit the for more information.