What it isA selective estrogen receptor modulator marketed in the U.S. only inside DUAVEE, paired with conjugated estrogens.
Why this oneThe pairing is the concept: bazedoxifene antagonizes the endometrium, letting menopausal estrogen therapy proceed without a progestin — a "tissue-selective estrogen complex."
What limits itSERM-class venous thromboembolism risk persists, and the combination is for women with a uterus who cannot or will not take progestins.
BOXED WARNING Endometrial cancer, cardiovascular disorders (stroke, DVT), and probable dementia; do not use estrogen therapy to prevent cardiovascular disease or dementia; do not take with additional estrogens.
FDA dosing
Population
Start
Target
Max
Moderate–severe vasomotor symptoms of menopause
Postmenopausal women with a uterus
1 tablet QD
1 tablet (CE 0.45 mg/bazedoxifene 20 mg) QD
1 tablet QD
Prevention of postmenopausal osteoporosis
Postmenopausal women with a uterus
1 tablet QD
1 tablet QD
1 tablet QD
Renal Not recommended (not studied in renal impairment)
Hepatic Contraindicated (hepatic impairment or disease)
Instructions
One tablet once daily, without regard to meals; swallow whole
Do not take with additional estrogens, progestins, or estrogen agonist/antagonists
Add supplemental calcium and/or vitamin D if dietary intake inadequate (osteoporosis prevention)
Use for the shortest duration consistent with treatment goals
Contraindications
Undiagnosed abnormal uterine bleeding
Known, suspected, or past history of breast cancer
Known or suspected estrogen-dependent neoplasia
Active or past venous thromboembolism (DVT/PE)
Active or past arterial thromboembolism (e.g., stroke, MI)
Known hepatic impairment or disease
Known protein C, protein S, or antithrombin deficiency or other thrombophilic disorders