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Drug Safety|September 13, 2012
First French experience of ADR reporting by patients after a mass immunization campaign with Influenza A (H1N1) pandemic vaccines: a comparison of reports submitted by patients and healthcare professionalsGeneviève Durrieu, Aurore Palmaro, Laure Pourcel, et al.Drug Safety|September 13, 2012
Effect of competition bias in safety signal generation: analysis of a research database of spontaneous reports in FranceAntoine Pariente, Paul Avillach, Francesco Salvo, et al.Drug Safety|June 19, 2012
Impact of regulatory guidances and drug regulation on risk minimization interventions in drug safety: a systematic reviewLenhangmbong Nkeng, Anne-Marie Cloutier, Camille Craig, et al.Drug Safety|June 19, 2012
A signal detection method to detect adverse drug reactions using a parametric time-to-event model in simulated cohort dataVictoria R Cornelius, Odile Sauzet, Stephen J W EvansDrug Safety|August 30, 2012
Patient versus healthcare professional spontaneous adverse drug reaction reporting: a systematic reviewJackie Inch, Margaret C Watson, Stella Anakwe-UmehDrug Safety|July 20, 2012
Drug interactions in dying patients: a retrospective analysis of hospice inpatients in GermanySebastian Frechen, Anna Zoeller, Klaus Ruberg, et al.Drug Safety|November 1, 1990
The relationship between oral contraceptive use, cancer and vascular diseaseC La Vecchia, S Franceschi, P Bruzzi, et al.Drug Safety|November 1, 1990
Recent developments in the toxicology of anabolic steroidsS Graham, M KennedyDrug Safety|January 1, 1991
Clinical features and management of adverse effects of quinolone antibacterialsJ H Paton, D S ReevesDrug Safety|July 23, 1998
The role of the WHO programme on International Drug Monitoring in coordinating worldwide drug safety effortsS OlssonPageof 311