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Bazedoxifene/​Conjugated Estrogens

    DEA Class; Rx

    Common Brand Names; Duavee

    • Estrogen Derivatives; 
    • Selective Estrogen Receptor Modulators

    Combination of estrogens derived from the urine of pregnant mares used with a selective estrogen receptor modulator (SERM) that helps to reduce endometrial hyperplasia
    Used in women with an intact uterus for menopausal-related hot flashes and for the prevention of osteoporosis
    Also helps relieve menopausal-related genitourinary symptoms

    Indicated for vasomotor symptoms associated with menopause

    Indicated for prevention of postmenopausal osteoporosis in nonhysterectomized women; when prescribing solely for the prevention of postmenopausal osteoporosis, therapy should only be considered for women at significant risk and nonestrogen medication should be carefully considered

    Should be used for the shortest duration consistent with treatment goals and risks for the individual woman

    Undiagnosed abnormal uterine bleeding

    Known, suspected, or past history of breast cancer

    Known or suspected estrogen-dependent neoplasia

    Active DVT, PE, or history of these conditions

    Active arterial thromboembolic disease (eg, stroke, MI) or history of these conditions

    Hypersensitivity (eg, anaphylaxis, angioedema) to estrogens, bazedoxifene, or any ingredients

    Known hepatic impairment or disease

    Known protein C, protein S, or antithrombin deficiency or other known thrombophilic disorders

    Pregnancy, women who may become pregnant, and nursing mothers; may cause fetal harm when administered to a pregnant woman

    • Muscle spasms (9%)
    • Nausea (8%)
    • Diarrhea (8%)
    • Dyspepsia (7%)
    • Upper abdominal pain (7%)
    • Oropharyngeal pain (7%)
    • Neck pain (5%)
    • Dizziness (5%)

    Should not take progestins, additional estrogens, or additional estrogen agonist/antagonists

    Estrogens and estrogen agonist/antagonists are known to increase risk of thromboembolism, including DVT, PE, and stroke

    Discontinue 4-6 weeks before surgery that is associated with increased risk of thromboembolism, or during periods of prolonged immobilization

    Absolute risk of dementia with estrogen-alone use vs placebo from the Women’s Health Initiative was 37 versus 25 cases per 10,000 women-years; relative risk was 1.49 A 2- to 4-fold risk of gallbladder disease requiring surgery is reported in postmenopausal women receiving estrogens

    Retinal vascular thrombosis reported

    Substantial increases in blood pressure described in a small number of case reports in women receiving estrogens; this effect was not observed in a large, randomized, placebo-controlled clinical study

    Estrogens may exacerbate pre-existing hypertriglyceridemia and lead to pancreatitis

    Caution with history of cholestatic jaundice associated with past estrogen use or with pregnancy

    Estrogen administration leads to increased thyroid-binding globulin (TBG) levels; women dependent on thyroid hormone replacement therapy who are also receiving estrogens may require increased thyroid hormone doses; patients dependent on thyroid hormone replacement therapy who are also receiving estrogens may require increased doses of thyroid replacement therapy; these patients should have their thyroid function monitored in order to maintain their free thyroid hormone levels in an acceptable range

    May cause fluid retention

    May exacerbate asthma, diabetes mellitus, epilepsy, migraine, porphyria, systemic lupus erythematosus, and hepatic hemangiomas

    Estrogens are metabolized partially by CYP3A4 and therefore coadministration with inhibitors and inducers of this isoenzyme may increase risk of toxicity or alter therapeutic effect

    Bazedoxifene undergoes metabolism by UGT enzymes in the intestinal tract and liver; coadministration with UGT inducers may reduce bazedoxifene exposure/efficacy and therefore increase risk of endometrial hyperplasia

    Do not use with conditions that predispose to hyperkalemia

    Retinal vascular thrombosis reported in patients receiving estrogens; discontinue medication pending examination if there is sudden partial or complete loss of vision, or a sudden onset of proptosis, diplopia, or migraine; if examination reveals papilledema or retinal vascular lesions, estrogens should be discontinued

    There are, possible risks that may be associated with use of progestins with estrogens compared to estrogen-alone regimens, including a possible increased risk of breast cancer, adverse effects on lipoprotein metabolism (e.g., lowering HDL, raising LDL), and impairment of glucose tolerance

    Use caution in individuals with severe hypocalcemia

    Contraindicated for use in pregnant women; not indicated for use in females of reproductive potential

    There are no data with the use of conjugated estrogens in pregnant women; however, epidemiologic studies and meta-analyses have not found an increased risk of genital and non-genital birth defects (including cardiac anomalies and limb-reduction defects) following exposure to combined hormonal contraceptives before conception or during early pregnancy

    Not indicated for use in females of reproductive potential

    Estrogens are present in human milk and can reduce milk production in breast-feeding females; this reduction can occur at any time but is less likely to occur once breast-feeding is well-established

    Adults

    1 tablet/day PO (conjugated estrogens 0.45 mg; bazedoxifene 20 mg).

    Geriatric

    1 tablet/day PO (conjugated estrogens 0.45 mg; bazedoxifene 20 mg).

    Adolescents

    Not indicated in premenopausal females.

    Children

    Not indicated.

    Infants

    Not indicated.

    Neonates

    Not indicated.

    Bazedoxifene/conjugated estrogens

    tablet

    • 20mg/0.45mg