Published on in Vol 6, No 2 (2018): Apr-Jun

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/10248, first published .
Adverse Drug Event Reporting From Clinical Care: Mixed-Methods Analysis for a Minimum Required Dataset

Adverse Drug Event Reporting From Clinical Care: Mixed-Methods Analysis for a Minimum Required Dataset

Adverse Drug Event Reporting From Clinical Care: Mixed-Methods Analysis for a Minimum Required Dataset

Journals

  1. Small S, Hohl C, Balka E. Organizational implications of implementing a new adverse drug event reporting system for care providers and integrating it with provincial health information systems. Healthcare Management Forum 2019;32(4):208 View
  2. Griffey R, Schneider R, Todorov A, Yaeger L, Sharp B, Vrablik M, Aaronson E, Sammer C, Nelson A, Manley H, Dalton P, Adler L, Pines J. Critical Review, Development, and Testing of a Taxonomy for Adverse Events and Near Misses in the Emergency Department. Academic Emergency Medicine 2019 View
  3. Hau J, Brasher P, Cragg A, Small S, Wickham M, Hohl C. Using ActionADE to create information continuity to reduce re-exposures to harmful medications: study protocol for a randomized controlled trial. Trials 2021;22(1) View

Books/Policy Documents

  1. Renuka D, Jeetha B. Proceedings of International Conference on Artificial Intelligence, Smart Grid and Smart City Applications. View