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Duavee
Conjugated Estrogens / Bazedoxifene
$579.00
0.45mg/20mg · 3 × 28 tablets · 3 months supply
BrandBranded medicine· By Pfizer
$193.00 per month
How long a supply?
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Annual cost
$2509a year at this pack size
Prescription required
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FDA boxed warningEndometrial cancer, cardiovascular disorders, and probable dementia
Women taking DUAVEE should not take additional estrogens
There is an increased risk of endometrial cancer in a woman with a uterus who uses unopposed estrogens. DUAVEE has been shown to reduce the risk of endometrial hyperplasia, which may be a precursor to endometrial cancer. Adequate diagnostic measures, including directed or random endometrial sampling when indicated, should be undertaken to rule out malignancy in postmenopausal women with undiagnosed persistent or recurring abnormal genital bleeding
Estrogen therapy should not be used for the prevention of cardiovascular disease or dementia
The Women's Health Initiative (WHI) estrogen-alone substudy reported increased risks of stroke and deep vein thrombosis (DVT) in postmenopausal women (50 to 79 years of age) during 7.1 years of treatment with daily oral conjugated estrogens (0.625 mg)-alone, relative to placebo
The WHI Memory Study (WHIMS) estrogen-alone ancillary study of WHI reported an increased risk of probable dementia in postmenopausal women 65 years of age and older during 5.2 years of treatment with daily conjugated estrogens (0.625 mg)-alone, relative to placebo. It is unknown whether this finding applies to younger postmenopausal women
Only daily oral 0.625 mg CE was studied in the estrogen-alone substudy of the WHI. Therefore, the relevance of the WHI findings regarding adverse cardiovascular events and dementia to lower CE doses, other routes of administration, or other estrogen-alone products is not known. Without such data, it is not possible to definitively exclude these risks or determine the extent of these risks for other products. Discuss with your patient the benefits and risks of estrogen-alone therapy, taking into account her individual risk profile.
Estrogens should be prescribed at the lowest effective doses and for the shortest duration consistent with treatment goals and risks for the individual woman.
About Duavee
Overview
Duavee is a prescription tablet containing conjugated estrogens and bazedoxifene for women who have a uterus. It is used to treat moderate to severe hot flashes associated with menopause and to prevent osteoporosis after menopause. It works through estrogen receptors, with bazedoxifene blocking estrogen activity in the uterus to reduce the risk of excessive thickening of the uterine lining. It should be used for the shortest time consistent with each woman’s treatment goals and risks.
What it treats
- Treatment of moderate to severe hot flashes associated with menopause in women with a uterus. - Prevention of osteoporosis after menopause in women with a uterus.
Safety information
Side effects
Common side effects include muscle spasms, nausea, diarrhea, indigestion, upper abdominal pain, throat pain, dizziness and neck pain. Serious risks include blood clots in the veins, lungs or blood vessels of the eye; stroke; cancer of the lining of the uterus, breast cancer or ovarian cancer; gallbladder disease; severely raised blood triglycerides; and jaundice caused by impaired bile flow. Contact a doctor promptly if any of these occur. Loss of vision requires urgent medical attention. The label advises stopping estrogen if loss of vision, severely raised triglycerides or jaundice caused by impaired bile flow occurs.
FDA boxed warning
Endometrial cancer, cardiovascular disorders, and probable dementia
Women taking DUAVEE should not take additional estrogens
There is an increased risk of endometrial cancer in a woman with a uterus who uses unopposed estrogens. DUAVEE has been shown to reduce the risk of endometrial hyperplasia, which may be a precursor to endometrial cancer. Adequate diagnostic measures, including directed or random endometrial sampling when indicated, should be undertaken to rule out malignancy in postmenopausal women with undiagnosed persistent or recurring abnormal genital bleeding
Estrogen therapy should not be used for the prevention of cardiovascular disease or dementia
The Women's Health Initiative (WHI) estrogen-alone substudy reported increased risks of stroke and deep vein thrombosis (DVT) in postmenopausal women (50 to 79 years of age) during 7.1 years of treatment with daily oral conjugated estrogens (0.625 mg)-alone, relative to placebo
The WHI Memory Study (WHIMS) estrogen-alone ancillary study of WHI reported an increased risk of probable dementia in postmenopausal women 65 years of age and older during 5.2 years of treatment with daily conjugated estrogens (0.625 mg)-alone, relative to placebo. It is unknown whether this finding applies to younger postmenopausal women
Only daily oral 0.625 mg CE was studied in the estrogen-alone substudy of the WHI. Therefore, the relevance of the WHI findings regarding adverse cardiovascular events and dementia to lower CE doses, other routes of administration, or other estrogen-alone products is not known. Without such data, it is not possible to definitively exclude these risks or determine the extent of these risks for other products. Discuss with your patient the benefits and risks of estrogen-alone therapy, taking into account her individual risk profile.
Estrogens should be prescribed at the lowest effective doses and for the shortest duration consistent with treatment goals and risks for the individual woman.
A boxed warning is the strongest warning the US Food and Drug Administration requires on a medicine label. Text is taken from the official label, with internal section references removed.
When to call your doctor
If symptoms are severe or getting worse quickly, seek emergency care rather than waiting.
Before taking this medicine
Do not take Duavee if you have unexplained abnormal uterine bleeding; known, suspected or previous breast cancer; known or suspected cancer that depends on estrogen; current or previous blood clots in the legs or lungs; or current or previous arterial blood clots, including stroke or heart attack. It must not be used if you have liver disease or impaired liver function, a known blood-clotting disorder such as protein C, protein S or antithrombin deficiency, or an allergy to estrogens, bazedoxifene or any ingredient. Do not take it during pregnancy, as it may harm the unborn baby. Do not take progestins, additional estrogens or other estrogen agonist/antagonist medicines while taking Duavee. Use is not recommended in women with impaired kidney function or those aged 75 or older, as these groups have not been studied. Warnings include blood clots, stroke, clots in the blood vessels of the eye, and cancers of the uterine lining, breast and ovaries. Estrogens increase the risk of gallbladder disease. Stop taking Duavee and seek medical advice if you develop loss of vision, severely raised triglycerides or jaundice caused by impaired bile flow. Thyroid function should be monitored if you take thyroid replacement therapy. An increased risk of probable dementia in women over 65 was reported in the Women’s Health Initiative Memory studies.
Using Duavee
Dosing
Dosing is set by your prescriber. Each health care professional may prescribe medication differently according to a patient's medical history and condition, so follow the directions on your prescription label and speak to your doctor or pharmacist before changing anything.
Storage
Store below 25°C in a dry place, in the original pack, away from direct light and moisture. Do not keep it in a bathroom. Keep all medicines out of the sight and reach of children.
Clinical information on this page is summarised from the US FDA label DUAVEE (CONJUGATED ESTROGENS/BAZEDOXIFENE) TABLET, FILM COATED [U.S. PHARMACEUTICALS] (DailyMed, retrieved 19 September 2026).
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