Work package 1

Review of consumer reporting of ADRs

Organizations: UMC, WHO, MPA, Lareb, NPSA, Zuellig

Objectives:

1) To review consumer reporting of ADRs.
2) To identify two consumer reporting methods that can be used to develop a pilot project on consumer reporting of ADRs.

Review of direct patient reporting of adverse drug reactions: Survey Report

A survey based on telephone interviews, email discussions and field visits of existing practices in consumer/patient reporting of adverse events relating to medicine use, was performed by Lareb, Florence van Hunsel PharmD, corresponding author, as part of Monitoring Medicines, FP7 Project funded by the European Commission.

REPORT

Review of direct patient reporting of adverse drug reactions D2.pdf

More for information plesae contact: Florence van Hunsel at F.vanHunsel@lareb.nl

PUBLICATION

Experiences with Adverse Drug Reaction.pdf

Work packages

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