Patient Pregnancy Registry

Share your experience to help improve knowledge about pregnancy after use of ellaOne®.

What is ellaOne®?

ellaOne® is a female emergency contraceptive pill to be taken within five days (120 hours) after unprotected sex or contraceptive failure (such as a missed pill, or a condom breaking during sex).

ellaOne® should only be used strictly in accordance with the Product Information (Package Leaflet). It is not intended to be used for any other purpose.

Should you need more information on ellaOne® or the registry, please contact your health care provider.

What is a Pregnancy registry?

A pregnancy registry is a voluntary program designed to collect medical information from individuals who were exposed to a medicine during pregnancy or just before pregnancy.

The existence of a registry does not mean that there is a risk for you or your baby if you have taken ellaOne® while you were pregnant. The goal is to better understand how the pregnancies progress and their outcomes after exposure to ellaOne®.

Why is participation important?

If you have inadvertently taken ellaOne® during your pregnancy or have become pregnant despite having taken ellaOne®, we are very interested in receiving more information about your pregnancy.

Sharing your experience helps :

• Improve scientific knowledge
• Support future users and health care providers
• Contribute to safety monitoring required by regulatory authorities

What does participation involve?

You may report information directly through this website or ask your physician to do it on your behalf. Your participation will not generate extra doctors’ visits nor lead you to take any medication. In all cases, you are strongly encouraged to contact your physician as early as possible in your pregnancy.

You will be asked to complete a secure questionnaire about :

• When you took ellaOne®
• Your menstrual and pregnancy history
• Any medical conditions or medications
• The course of your pregnancy
• The outcome of the pregnancy
• Your baby’s health after birth

You may also consent for your health care provider to share follow‑up clinical information, which helps ensure accuracy and completeness.

Privacy and confidentiality

Your identity will remain strictly confidential.

Any information would strictly be handled in an anonymous manner in order to preserve your confidentiality. The electronic system stores your data securely, and only anonymised data are used for processing and reporting purposes. No identifying information will appear in any reports or publications.

Your contact information is used solely to send automated reminders for follow‑up and to request clarification if needed.