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  • Myovant Patient Assistance Program
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Myovant Patient Assistance Program

The Myovant Patient Assistance Program can provide an ongoing supply of Myfembree at no cost to eligible patients with a coverage denial or no insurance coverage

The Myovant Patient Assistance Program can provide a supply of Myfembree as long as the eligibility criteria are being met and maintained. Free medication supply is fulfilled by TC Script, a noncommercial dispensing pharmacy. Additional terms and conditions apply and can be found below.

The Myovant Sciences Patient Assistance Program (“Program”) provides Myfembree at no cost to eligible patients who are prescribed Myfembree for an FDA-approved indication. Patients and prescribers must complete the Myfembree Support Program enrollment form, and prescribers must provide a Patient Assistance Program prescription. Patients must meet Program eligibility requirements, which include, but are not limited to, lack of insurance coverage for Myfembree, financial criteria and income evaluation, and patients must be residents of the United States and US Territories. Program requires annual re-evaluation and re-enrollment for continued participation. Patients may be asked to reverify insurance coverage status during the course of the Program. Patient and participating prescribers agree not to seek reimbursement for all, or any part of, the free product received by the patient through this Program. Patients may not count the free product received from the Myfembree Support Program as an expense incurred for purposes of determining out-of-pocket costs for any plan, including true out-of-pocket costs (“TrOOP”) for purposes of calculating the out-of-pocket threshold for Medicare Part D plans. Government health insured patients who meet the Program eligibility criteria are eligible to receive free product for the entire coverage year, and Myovant Sciences will notify patients’ government health insurance plans that the patient is enrolled in the Program. No purchase necessary. Program is not health insurance, nor is participation a guarantee of insurance coverage. Other limitations may apply. Myovant Sciences reserves the right to rescind, revoke, or amend the Program and discontinue support at any time without notice.

Enrolling in the Myfembree® Support Program

Call to speak to dedicated support staff who will guide you through the enrollment process.

1-833-MYFEMBREE (1-833-693-3627), 8 AM–8 PM ET, Monday–Friday.

Please see your prescribing doctor or call the Myfembree® Support Program for enrollment assistance. Once you are enrolled, the support program team can provide specific information to help you understand your insurance benefits and coverage for Myfembree.

IMPORTANT SAFETY INFORMATION

USE

What is the most important information I should know about Myfembree?

Myfembree may cause serious side effects, including:

  • cardiovascular conditions
    • Myfembree may increase your chances of heart attack, stroke, or blood clots, especially if you are over 35 years of age, smoke, and have uncontrolled high blood pressure. Stop taking Myfembree and call your healthcare provider right away or go to the nearest hospital emergency room right away if you have:

Myfembree is a prescription medicine used to control heavy menstrual bleeding due to uterine fibroids in premenopausal women (before “change of life” or menopause). It should not be taken for more than 24 months. It is not known if Myfembree is safe and effective in children under 18 years of age.

Myfembree contains relugolix, which reduces the amount of estrogen (and other hormones) produced by ovaries, estradiol (an estrogen) which may reduce the risk of bone loss, and norethindrone acetate (a progestin) which is necessary when women with a uterus (womb) take estrogen.

USE

Myfembree is a prescription medicine used to control heavy menstrual bleeding due to uterine fibroids in premenopausal women (before “change of life” or menopause). It should not be taken for more than 24 months.

IMPORTANT SAFETY INFORMATION

What is the most important information I should know about Myfembree?

Myfembree may cause serious side effects, including:

  • cardiovascular conditions
    • Myfembree may increase your chances of heart attack, stroke, or blood clots, especially if you are over 35 years of age, smoke, and have uncontrolled high blood pressure. Stop taking Myfembree and call your healthcare provider right away or go to the nearest hospital emergency room right away if you have:
      • leg pain or swelling that will not go away
      • sudden shortness of breath
      • double vision, bulging of the eyes, sudden blindness, partial or complete
      • pain or pressure in your chest, arm, or jaw
      • sudden, severe headache unlike your usual headaches
      • weakness or numbness in an arm or leg, or trouble speaking
  • bone loss (decreased bone mineral density)
    • While you are taking Myfembree, your estrogen levels may be low. Low estrogen levels can lead to bone mineral density loss.
    • If you have bone loss on Myfembree, your bone density may improve after you stop taking Myfembree, but complete recovery may not occur. It is unknown if these bone changes could increase your risk for broken bones as you age. For this reason, you should not take Myfembree for more than 24 months.
    • Your healthcare provider may order an X-ray test called a DXA scan to check your bone mineral density when you start taking Myfembree and periodically after you start.
    • Your healthcare provider may advise you to take vitamin D and/or calcium supplements as part of a healthy lifestyle that promotes bone health. If you are also advised to take iron supplements, they should be taken at least two hours apart from your vitamin D or calcium supplements.

USE

Myfembree is a prescription medicine used to control heavy menstrual bleeding due to uterine fibroids in premenopausal women (before “change of life” or menopause). It should not be taken for more than 24 months. It is not known if Myfembree is safe and effective in children under 18 years of age.

Myfembree contains relugolix, which reduces the amount of estrogen (and other hormones) produced by ovaries, estradiol (an estrogen) which may reduce the risk of bone loss, and norethindrone acetate (a progestin) which is necessary when women with a uterus (womb) take estrogen.

IMPORTANT SAFETY INFORMATION

What is the most important information I should know about Myfembree?

Myfembree may cause serious side effects, including:

  • cardiovascular conditions
    • Myfembree may increase your chances of heart attack, stroke, or blood clots, especially if you are over 35 years of age, smoke, and have uncontrolled high blood pressure. Stop taking Myfembree and call your healthcare provider right away or go to the nearest hospital emergency room right away if you have:
      • leg pain or swelling that will not go away
      • sudden shortness of breath
      • double vision, bulging of the eyes, sudden blindness, partial or complete
      • pain or pressure in your chest, arm, or jaw
      • sudden, severe headache unlike your usual headaches
      • weakness or numbness in an arm or leg, or trouble speaking
  • bone loss (decreased bone mineral density)
    • While you are taking Myfembree, your estrogen levels may be low. Low estrogen levels can lead to bone mineral density loss.
    • If you have bone loss on Myfembree, your bone density may improve after you stop taking Myfembree, but complete recovery may not occur. It is unknown if these bone changes could increase your risk for broken bones as you age. For this reason, you should not take Myfembree for more than 24 months.
    • Your healthcare provider may order an X-ray test called a DXA scan to check your bone mineral density when you start taking Myfembree and periodically after you start.
    • Your healthcare provider may advise you to take vitamin D and/or calcium supplements as part of a healthy lifestyle that promotes bone health. If you are also advised to take iron supplements, they should be taken at least two hours apart from your vitamin D or calcium supplements.
  • effects on pregnancy
    • Do not take Myfembree if you are trying to become pregnant or are pregnant. It may increase the risk of early pregnancy loss.
    • If you think you are pregnant, stop taking Myfembree right away and call your healthcare provider.
      • If you become pregnant while taking Myfembree, you are encouraged to enroll in the Pregnancy Registry. The purpose of the pregnancy registry is to collect information about the health of you and your baby. Talk to your healthcare provider or call 1-(855) 428-0707.
    • Myfembree can decrease your menstrual bleeding or result in no menstrual bleeding at all, making it hard to know if you are pregnant. Watch for other signs of pregnancy such as breast tenderness, weight gain and nausea.
    • Myfembree does not prevent pregnancy. You will need to use effective methods of birth control while taking Myfembree and for 1 week after you stop taking Myfembree. Examples of effective methods can include condoms or spermicide, which do not contain hormones.
    • Do not take hormonal birth control such as birth control pills, because they may increase your side effects and Myfembree may not work as well.

Talk to your healthcare provider about which birth control to use during treatment with Myfembree. Your healthcare provider may change the birth control you were on before you start taking Myfembree.

Do not take Myfembree if you:

  • have or have had:
    • blood clots in your legs (deep vein thrombosis), lungs (pulmonary embolism), or eyes (retinal thrombosis)
    • stroke or heart attack
    • a problem that makes your blood clot more than normal
    • blood circulation disorders
    • certain heart valve problems or heart rhythm abnormalities that can cause blood clots to form in the heart
    • high blood pressure not well controlled by medicine
    • diabetes with kidney, eye, nerve, or blood vessel damage
    • certain kinds of severe migraine headaches with aura, numbness, weakness or changes in vision or migraine headaches if you are over age 35
    • breast cancer or any cancer that is sensitive to female hormones
    • osteoporosis
    • vaginal bleeding that has not been diagnosed. Your healthcare provider should check any unexplained vaginal bleeding to find out the cause.
    • liver problems including liver disease
  • smoke and are over 35 years old
  • have had a serious allergic reaction with symptoms that included swelling of your face, lips, mouth or tongue, trouble breathing, skin rashes, redness, or swelling or an allergic reaction to relugolix, estradiol, norethindrone or any of the ingredients in Myfembree. See the end of this Important Safety Information for a complete list of ingredients in Myfembree.

Before you take Myfembree, tell your healthcare provider about all of your medical conditions including if you:

  • have or have had:
    • broken bones or other conditions that may cause bone problems.
    • depression, mood swings, or suicidal thoughts or behavior.
    • yellowing of the skin or eyes (jaundice) or jaundice caused by pregnancy (cholestasis of pregnancy).
  • are scheduled for surgery or will be on bed rest. Myfembree may increase your risk of blood clots after surgery. Your healthcare provider may advise you to stop taking Myfembree before you have surgery. Talk to your healthcare provider about when to stop Myfembree before surgery and when to restart Myfembree after surgery.
  • are pregnant or think you may be pregnant or just had a baby.
  • are breastfeeding. Myfembree may pass into your breast milk. Talk to your healthcare provider about the best way to feed your baby if you take Myfembree.

Tell your healthcare provider about all the medicines you take, including prescription, over-the-counter medicines, vitamins, and herbal supplements.

Women on thyroid or cortisol replacement therapy may need increased doses of the hormone.

Know the medicines you take. Keep a list of your medicines with you to show to your healthcare provider and pharmacist when you get a new medicine.

How should I take Myfembree?

  • Take Myfembree exactly as your healthcare provider tells you to take it.
  • Take Myfembree 1 time each day at about the same time with or without food.
  • If you have to take oral P-gp inhibitors, take Myfembree first and wait at least 6 hours before taking the P-gp inhibitor. Ask your healthcare provider if you are not sure if you are taking this type of medicine.
  • Your healthcare provider may give you a pregnancy test before you start taking Myfembree.
  • You should begin Myfembree as soon as possible after your period begins, but no later than 7 days after your period has started. If you start Myfembree on another day, your period may become heavy or irregular for the first month after starting treatment, but bleeding should decrease after this time.
  • If you take too much Myfembree, call your healthcare provider or go to the nearest hospital emergency room right away.
  • If you miss a dose, take the missed dose as soon as you remember on that day, and then take Myfembree at the usual time the next day.
  • Do not take 2 doses at once to make up for the missed dose. If you do not remember until you are due for Myfembree on the next day, do not make up for the missed dose.

What are the possible side effects of Myfembree?

Myfembree may cause serious side effects including:

  • See “What is the most important information I should know about Myfembree?”
  • suicidal thoughts, suicidal behavior, and worsening of mood. Call your healthcare provider or get emergency medical help right away if you have any of these symptoms, especially if they are new, worse, or bother you:
    • thoughts about suicide or dying
    • attempts to commit suicide
    • new or worse depression
    • new or worse anxiety
    • other unusual changes in behavior or mood

    Pay attention to any changes, especially sudden changes in your mood, behaviors, thoughts, or feelings.

  • abnormal liver tests. Call your healthcare provider right away if you have any of these signs and symptoms of liver problems:
    • jaundice
    • dark amber-colored urine
    • feeling tired (fatigue or exhaustion)
    • nausea and vomiting
    • generalized swelling
    • right upper stomach area (abdomen) pain
    • bruising easily
  • gallbladder problems (cholestasis), especially if you had cholestasis of pregnancy.
  • high blood pressure. See your healthcare provider to check your blood pressure regularly.
  • uterine fibroid prolapse or expulsion. Fibroids can come out completely or partially through the vagina. Call your healthcare provider right away if you have increased bleeding from the vagina, which can be serious, or cramping, while taking Myfembree.
  • hair loss (alopecia). Hair loss and hair thinning can happen while taking Myfembree. It is not known if this hair loss or hair thinning stops after you stop taking Myfembree or is reversible. Talk to your healthcare provider if this is a concern for you.
  • increases in the blood sugar, cholesterol and fat (triglycerides) levels in your blood.
  • changes in laboratory tests including thyroid, steroid, hormone, cholesterol, and blood clotting tests.

The most common side effects of Myfembree include:

  • hot flushes
  • increased sweating
  • night sweats
  • abnormal vaginal bleeding (bleeding that lasts too long, is too much, or is unexpected)
  • hair loss or hair thinning
  • decreased interest in sex

These are not all the possible side effects of Myfembree. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

How should I store Myfembree?

  • Store Myfembree at room temperature between 59°F to 86°F (15°C to 30°C).
  • Dispose of unused medicines through community take-back disposal programs when available. If no community take-back disposal program is available go to www.fda.gov/drugdisposalfor information on how to dispose of Myfembree the right way.
  • Do not flush Myfembree down the toilet.
  • Do not keep medicine that is out of date or that you no longer need.
  • Keep Myfembree and all medicines out of the reach of children

General information about the safe and effective use of Myfembree.

Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use Myfembree for a condition for which it was not prescribed. Do not give Myfembree to other people, even if they have the same symptoms that you have. It may harm them. You can ask your healthcare provider or pharmacist for information about Myfembree that is written for health professionals.

What are the ingredients of Myfembree?

Active ingredient: relugolix, estradiol, and norethindrone acetate

Inactive ingredients: lactose monohydrate, mannitol, sodium starch glycolate, hydroxypropyl cellulose, magnesium stearate, hypromellose, titanium dioxide, triacetin, iron oxide yellow.

Manufactured by: Patheon Inc., Mississauga, Ontario, Canada

Manufactured for: Myovant Sciences, Brisbane, CA 94005

For more information, call Myovant Sciences at 1-833-MYOVANT (1-833-696-8268) or go to www.Myfembree.com

Please see full Prescribing Information, including BOXED WARNINGand Patient Information

©2021 Myovant Sciences GmbH and Pfizer Inc. All rights reserved. PP-US-REL-CT-2100247 10/21

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