Prognia
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🇪🇺EU · EMAAuthorisedATC: G03XC02

Conbriza(bazedoxifene)

Osteoporosis, Postmenopausal

Marketing Authorisation Holder: Pfizer Europe MA EEIG

EMA Authorisation: 17/04/2009

INN: bazedoxifene

Indication

Conbriza is indicated for the treatment of postmenopausal osteoporosis in women at increased risk of fracture. A significant reduction in the incidence of vertebral fractures has been demonstrated; efficacy on hip fractures has not been established. When determining the choice of Conbriza or other therapies, including oestrogens, for an individual postmenopausal woman, consideration should be given to menopausal symptoms, effects on uterine and breast tissues, and cardiovascular risks and benefits.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.