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EMA Product

Evista

Product approved by European Medicines Agency (EU)

Basic Information

Evista

Regulatory Information

EMEA/H/C/000184

Authorised

August 5, 1998

April 22, 1998

31

April 1, 2025

Company Information

France

24 rue Erlanger 75016 Paris

SUBSTIPHARM

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Evista is indicated for the treatment and prevention of osteoporosis in post-menopausal women. A significant reduction in the incidence of vertebral, but not hip fractures has been demonstrated. When determining the choice of Evista 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.

Overview Summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the studies performed, to reach their recommendations on how to use the medicine. If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis of the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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