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Bazedoxifene

(in DUAVEE)

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.

FDA label

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 dosingPopulationStartTargetMax
Moderate–severe vasomotor symptoms of menopausePostmenopausal women with a uterus1 tablet QD1 tablet (CE 0.45 mg/bazedoxifene 20 mg) QD1 tablet QD
Prevention of postmenopausal osteoporosisPostmenopausal women with a uterus1 tablet QD1 tablet QD1 tablet QD

Renal Not recommended (not studied in renal impairment)

Hepatic Contraindicated (hepatic impairment or disease)

Instructions

Contraindications

Cautions

Adverse reactions

Pregnancy Contraindicated in pregnancy; may cause fetal harm.

Lactation Not indicated in females of reproductive potential; estrogens present in milk and can reduce milk production.

NO BOXED WARNINGS

Classes and tags

Clinical profile

Direct muscarinic antagonism0 / 4

Mechanism of action: Bazedoxifene ballicule

Bazedoxifene ballicule: receptor binding, kinetics and half-life diagram

Open Bazedoxifene in the interactive console ↗