MedPath
EMA Product

Rapiscan

Product approved by European Medicines Agency (EU)

Basic Information

Rapiscan

Regulatory Information

EMEA/H/C/001176

Authorised

September 6, 2010

15

May 24, 2023

Company Information

Norway

GE Healthcare AS Nycoveien 1 NO-0485 Oslo

GE Healthcare AS

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication This medicinal product is for diagnostic use only. Rapiscan is a selective coronary vasodilator for use as a pharmacological stress agent for radionuclide myocardial perfusion imaging (MPI) in adult patients unable to undergo adequate exercise stress.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Rapiscan. 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 Rapiscan.

© Copyright 2025. All Rights Reserved by MedPath