This is a summary of the European public assessment report (EPAR) for Conbriza. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Conbriza.
Therapeutic Indication
### Therapeutic 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.
Therapeutic Area (MeSH)
ATC Code
G03XC02
ATC Item
bazedoxifene
Pharmacotherapeutic Group
Sex hormones and modulators of the genital system
Active Substance (Summary)
INN / Common Names
| Substance | CAS | Monograph |
|---|---|---|
| bazedoxifene | N/A | 巴多昔芬 |
EMA Name
Conbriza
Medicine Name
Conbriza
Aliases
N/ANo risk management plan link.
