Patient information: uses, side effects, how to take - Vyepti
What is VYEPTI?
VYEPTI is a prescription medicine used for the preventive treatment of migraine in adults.
It is not known if VYEPTI is safe and effective in children.
Do not receive VYEPTI if you are allergic to eptinezumab-jjmr or any of the ingredients in VYEPTI. See the end of this Patient Information leaflet for a complete list of ingredients in VYEPTI.
Before you receive VYEPTI, tell your healthcare provider about all of your medical conditions, including if you:
- have high blood pressure.
- have circulation problems in your fingers and toes.
are pregnant or plan to become pregnant. It is not known if VYEPTI will harm your unborn baby.
- Pregnancy Registry: There is a pregnancy registry for women who take VYEPTI. The purpose of this registry is to collect information about the health of you and your baby. You may enroll yourself by calling 1-855-810-8549 or by visiting www.vyeptipregnancyregistry.lundbeck.com. Or you may talk to your healthcare provider about how you can take part in this registry.
- are breastfeeding or plan to breastfeed. It is not known if VYEPTI passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby while using VYEPTI.
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
How will I receive VYEPTI?
- VYEPTI will be given by a healthcare provider in a healthcare setting.
- VYEPTI is given by intravenous (IV) infusion in your vein.
- VYEPTI will be given over 30 minutes every 3 months.
If you have questions about your infusion schedule, ask your healthcare provider.
What are the possible side effects of VYEPTI?
VYEPTI may cause serious side effects, including:
Allergic reactions. Allergic reactions can happen after receiving VYEPTI. Call your healthcare provider or get emergency medical help right away if you have any of the following symptoms of an allergic reaction:
- rash
- swelling of your face, lips, tongue or throat
- trouble breathing
- hives
- redness in your face
- Constipation with serious complications. Severe constipation can happen after receiving VYEPTI. In some cases, people have been hospitalized. Contact your healthcare provider if you have severe constipation or constipation is associated with symptoms such as severe or constant belly pain, vomiting, swelling of belly, or bloating.
- High blood pressure. High blood pressure or worsening of high blood pressure can happen after receiving VYEPTI. Contact your healthcare provider if you have an increase in blood pressure.
- Raynaud’s phenomenon. A type of circulation problem can worsen or happen after receiving VYEPTI. Raynaud’s phenomenon can lead to your fingers or toes feeling numb, cool, or painful, or changing color from pale, to blue, to red. Contact your healthcare provider if these symptoms occur.
The most common side effects of VYEPTI include:
- stuffy nose and scratchy throat
- allergic reactions
These are not all of the possible side effects of VYEPTI.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
General information about the safe and effective use of VYEPTI.
Medicines are sometimes prescribed for purposes other than those listed in the Patient Information leaflet.
You can ask your pharmacist or healthcare provider for information about VYEPTI that is written for health professionals.
What are the ingredients in VYEPTI?
Active ingredient: eptinezumab-jjmr
Inactive ingredients: L-histidine, L-histidine hydrochloride monohydrate, polysorbate 80, sorbitol, and Water for Injection.
The vial stopper is not made with natural rubber latex.
Manufactured by: Lundbeck Seattle BioPharmaceuticals, Inc., 11804 North Creek Parkway South, Bothell, WA 98011
US License Number: 2097

Vyepti is a registered trademark of Lundbeck Seattle BioPharmaceuticals, Inc.
For more information, call 1-833-4-VYEPTI (833-489-3784) or go to www.Vyepti.com
This Patient Information has been approved by the U.S. Food and Drug Administration. Revised: 06/2026
