FAQs

The BLOOM Pregnancy Registry is sponsored by AbbVie Inc. It was created to help doctors better understand if medications containing elagolix, like ORIAHNN^® (elagolix, estradiol, and norethindrone acetate capsules; elagolix capsules), have any effect on pregnancy, delivery, or the health of babies. Some women taking part in this registry will have been prescribed a medication containing elagolix, like ORIAHNN, by their doctor. However, they became pregnant while taking it.

Information from the following 2 groups will be evaluated:

• women who were exposed to an elagolix-containing medication, like ORIAHNN, during early pregnancy
• women who were not taking ORIAHNN when they became pregnant, but who have uterine fibroids.

Important Safety Information: ORIAHNN should not be taken by women who are pregnant or trying to become pregnant. It may increase the risk of early pregnancy loss. If you think you are pregnant, stop taking ORIAHNN right away and call your healthcare provider.

Women can help by sharing their experiences throughout their pregnancy and information on the health of their babies until they are 12 months old.

You will be contacted by a registry representative when you join the registry, and then once during each trimester of your pregnancy. After you have given birth, you will be contacted about 4 weeks after your delivery and again when your baby is 6 and 12 months old. Your healthcare providers will also be contacted 2 times during your pregnancy, and once after you deliver. Your baby’s healthcare provider will be contacted when your baby is 6 and 12 months old. You will not be asked to attend extra visits at a healthcare provider’s office, change anything you usually do, or change any treatments that you currently receive for the duration of your participation in the registry.

If you would like further information to discuss with a family member or your regular doctor, or to share with others, you can download a copy of the BLOOM Pregnancy Registry Patient Brochure.

This registry is a research study. For the protection of all participants, research studies are reviewed by an Institutional Review Board (IRB). An IRB is a group of scientific and non-scientific individuals who perform an ongoing ethical review of the registry with the participant’s rights and welfare in mind. An IRB has approved this study. The consent form (also approved by the IRB) that the registry representative will read and review with you, explains the study in detail and lets you know your rights. It also outlines your role as a participant in the study. You will be provided with a copy of the consent form.

The BLOOM Pregnancy Registry was created to help doctors better understand if medications containing elagolix, like ORIAHNN, have any effect on pregnancy, delivery, or the health of babies. Registry representatives will collect information from pregnant women who have taken an elagolix-containing medication during pregnancy, and/or who have uterine fibroids. By sharing your experience, you could help other women and their doctors to better understand if elagolix-containing medications have any effect on pregnancy, delivery, or the health of babies.

No. Participation in this registry does not offer direct access to any medical services or advice. It also does not endorse or provide any healthcare product or service. If you have any questions about your healthcare, please talk to your healthcare provider.

Women with uterine fibroids who are pregnant and have received an elagolix-containing medication, like ORIAHNN, at any time during pregnancy may be eligible. You may also join the registry if you have uterine fibroids, and are pregnant but have not received ORIAHNN. Your eligibility for participation will be confirmed by a registry representative before you join the registry.

After you decide that you want to join the BLOOM pregnancy registry and give your verbal informed consent, you will need to answer a few questions to see if you are eligible for participation.

If you are eligible to take part, you will be asked to provide additional information about yourself, your health and your pregnancy. You will be contacted when you first consent to be a part of the registry, and then once during each trimester of your pregnancy. After you have given birth, you will be contacted about 4 weeks after your delivery and when your baby is 6 and 12 months old. Your healthcare providers will also be contacted after you consent to be part of the registry, 2 times during your pregnancy, and once after your delivery. Your baby’s healthcare provider will be contacted when your baby is 6 and 12 months old. You will not be asked to attend extra visits at a healthcare provider’s office, change anything you usually do, or change any treatments that you currently receive for the duration of your participation in the registry.

If you join this registry, your involvement will last for the duration of your pregnancy and until your baby is at least 12 months old.

Your initial telephone interview upon consenting for the registry may last approximately 45 minutes. The follow-up telephone calls that will be made once per trimester and after your delivery will last approximately 10–15 minutes each.

There is no cost to you for joining the registry. Please check with your service provider about any charges that may be associated with receiving text messages if you decide you want to receive text message reminders from the registry team.

Yes, you will be paid up to $75 for answering questions during your first call, and up to $25 for each additional call. In total, up to $225 could be paid to you if you complete all calls.

Although it is a good idea to notify your healthcare provider about your participation in the registry, their permission is not required. As part of your agreement to be in the study, you will give your and your baby’s healthcare providers permission to share information about you and your baby.

We must collect your personal contact information so that we can send you emails and call you to complete the telephone assessments. Your personal contact information will be stored separately from your medical information. This means that researchers reviewing the data will not have access to your personal contact information.

We will use your information for research purposes. We will collect information about your identity, health, and the health of your baby. The information you provide may help researchers gain insight into the use of elagolix-containing medications during pregnancy.

The information you provide in telephone interviews will not be associated with your name, your baby’s name, or your contact details. Your personal identifying information will not be shared with AbbVie Inc., the Sponsor of this registry. In any presentation of results from this registry, your identity will remain anonymous and confidential. The information is expected to be kept for 15 years after the completion of the registry, and may be kept longer.

For questions about the BLOOM Pregnancy Registry, please contact a registry representative at BloomPregnancyRegistry@IQVIA.com or use the registry’s toll-free number 1-(833)-782-7241.

You can change your contact information at any time. Simply click the link in any of our emails to update your contact information, contact the registry team at BloomPregnancyRegistry@IQVIA.com or use the registry’s toll-free number 1-(833)-782-7241.

Your participation in this registry is voluntary; you may withdraw your consent at any time. If you decide you no longer want to participate, please contact us on the registry’s toll-free number
1-(833)-782-7241.

To learn more about our Privacy Policy and how your information will be used, please visit our Privacy Policy page.

Please contact your healthcare provider with any questions about your pregnancy.