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Drug Safety|May 2, 2018
Non-bleeding Adverse Events with the Use of Direct Oral Anticoagulants: A Sequence Symmetry AnalysisGéric Maura, Cécile Billionnet, Joël Coste, et al.Drug Safety|April 17, 2019
Correction to: A Machine-Learning Algorithm to Optimise Automated Adverse Drug Reaction Detection from Clinical CodingChristopher McMaster, David Liew, Claire Keith, et al.Drug Safety|August 18, 2018
The Prevalence of Dose Errors Among Paediatric Patients in Hospital Wards with and without Health Information Technology: A Systematic Review and Meta-AnalysisPeter J Gates, Sophie A Meyerson, Melissa T Baysari, et al.Drug Safety|August 22, 2018
Enhancing Pharmacovigilance Capabilities in the EU Regulatory Network: The SCOPE Joint ActionAnna Radecka, Louise Loughlin, Mick Foy, et al.Drug Safety|August 28, 2018
Proton Pump Inhibitor Use and Risk of Developing Alzheimer's Disease or Vascular Dementia: A Case-Control AnalysisPatrick Imfeld, Michael Bodmer, Susan S Jick, et al.Drug Safety|October 16, 2012
Reasons for and time to discontinuation of rimonabant therapy: a modified prescription-event monitoring studyMarjolein J C Willemen, Aukje K Mantel-Teeuwisse, Yvonne Buggy, et al.Drug Safety|October 16, 2012
Challenges of drug risk communications in the PhilippinesKenneth Hartigan-GoDrug Safety|March 20, 2010
Adverse drug reactions in the paediatric population in Denmark: a retrospective analysis of reports made to the Danish Medicines Agency from 1998 to 2007Lise Aagaard, Camilla Blicher Weber, Ebba Holme HansenDrug Safety|August 20, 2025
Navigating Medical Device Safety: Current Status, Challenges, and Future Regulatory DirectionsOmar Aimer, Catherine BaldridgeDrug Safety|February 24, 2023
Use of Structured Electronic Health Records Data Elements for the Development of Computable Phenotypes to Identify Potential Adverse Events Associated with Intravenous Immunoglobulin InfusionJillian H Hurst, Amanda Brucker, Congwen Zhao, et al.Pageof 311