[Improving adverse drug reaction reporting by general practitioners through clinical research assistants visits].


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… (More)
DOI: 10.1016/j.therap.2016.09.004