This paper is in the following e-collection/theme issue:

Pharmacovigilance (138) Adverse Drug Events Detection, Pharmacovigilance and Surveillance (159) Safety and Error Prevention in Health (206)

Published on in Vol 4, No 1 (2018): Jan-Mar

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/9282, first published .
Why Clinicians Don’t Report Adverse Drug Events: Qualitative Study

Why Clinicians Don’t Report Adverse Drug Events: Qualitative Study

Why Clinicians Don’t Report Adverse Drug Events: Qualitative Study

Authors of this article:

Corinne M Hohl1, 2, 3 Author Orcid Image ;   Serena S Small1, 4 Author Orcid Image ;   David Peddie1, 4 Author Orcid Image ;   Katherin Badke5 Author Orcid Image ;   Chantelle Bailey1, 2 Author Orcid Image ;   Ellen Balka1, 4 Author Orcid Image
Article Authors Cited by (42) Tweetations (41) Metrics

Corinne M Hohl   1, 2, 3 * , MHSc, MD, FRCPC ;   Serena S Small   1, 4 * , MA ;   David Peddie   1, 4 * , BEng, MA ;   Katherin Badke   5 * , BSc (Pharm) ;   Chantelle Bailey   1, 2 , MSc, PhD ;   Ellen Balka   1, 4 * , PhD

1 Centre for Clinical Epidemiology and Evaluation, Vancouver Coastal Health Research Institute, Vancouver, BC, Canada

2 Department of Emergency Medicine, University of British Columbia, Vancouver, BC, Canada

3 Vancouver General Hospital Emergency Department, Vancouver, BC, Canada

4 School of Communication, Simon Fraser University, Burnaby, BC, Canada

5 Department of Pharmaceutical Sciences, Vancouver General Hospital, Vancouver, BC, Canada

*these authors contributed equally

Corresponding Author:

  • Corinne M Hohl, MHSc, MD, FRCPC
  • Centre for Clinical Epidemiology and Evaluation
  • Vancouver Coastal Health Research Institute
  • 828 West 10th Ave, 7th Fl.
  • Vancouver, BC
  • Canada
  • Phone: 1 604 875 4111 ext 63467
  • Email: chohl@mail.ubc.ca