| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5559080 | Thérapie | 2017 | 5 Pages |
Abstract
The main limitation of adverse drug reactions (ADRs) reporting, particularly by general practitioners (GP), to the regional pharmacovigilance centers is under-reporting. The Midi-Pyrénées Regional Pharmacovigilance Center (South western, France) sets up regular visits by a clinical research assistant (CRA) to GP in order to increase the number of ADR reports. The aim of this pilot study was to assess the effect of regular visits of a CRA in GPs offices on the rate of ADR reporting. After one year, CRA visits permit a two-fold increase in ADR reporting.
Keywords
Related Topics
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Pharmacology, Toxicology and Pharmaceutical Science
Pharmacology, Toxicology and Pharmaceutics (General)
Authors
Geneviève Durrieu, Julien Jacquot, Dominique Baudrin, Mathilde Mège, Vanessa Rousseau, Haleh Bagheri, Emmanuelle Bondon-Guitton, Delphine Abadie, François Montastruc, Michel Bismuth, Stéphane Oustric, Jean-Louis Montastruc,