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EMA Product

Quadramet

Product approved by European Medicines Agency (EU)

Basic Information

Quadramet

Regulatory Information

EMEA/H/C/000150

Authorised

February 4, 1998

15

June 3, 2015

Company Information

France

Route Nationale 306, Saclay B.P. 32 F-91192 Gif sur Yvette Cedex

CIS BIO INTERNATIONAL

Active Ingredients

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Quadramet is indicated for the relief of bone pain in patients with multiple painful osteoblastic skeletal metastases which take up technetium \[99mTc\]-labelled biphosphonates on bone scan. The presence of osteoblastic metastases which take up technetium \[99mTc\]-labelled biphosphonates should be confirmed prior to therapy.

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 its 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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