The second database, the PROTECT ADR database, is a listing of all ADRs contained in the section 4.8 of the summary of product characteristics (SmPC) of medicinal products centrally authorised in the EU. It is based on the Medical Dictionary for Regulatory Activities (MedDRA) terminology. The goal of this database is to improve the efficiency of the detection process of ADRs by allowing quick identification and filtering or flagging of listed and unlisted ADR. This database is updated every 6 months and currently contains information up to 30 June 2012.
For further information, please visit:
http://www.imi-protect.eu
About PROTECT
The goal of PROTECT is to strengthen the monitoring of the benefit-risk of medicines in Europe by developing innovative methods. These methods aim to:
- enhance early detection and assessment of adverse drug reactions (ADRs) from different data sources (clinical trials, spontaneous reporting and observational studies);
- enable the integration and presentation of data on benefits and risks.
PROTECT is receiving funding from the European Community's Seventh Framework Programme (FP7/2007-2013) through the Innovative Medicine InitiativeExternal link icon. The Agency coordinates the project and manages a multi-national consortium of 33 partners including academics, regulators and companies.