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
Available strengths
tab 20/0.45 mg
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