190 related articles for article (PubMed ID: 27538362)
1. Designing an Adverse Drug Event Reporting System to Prevent Unintentional Reexposures to Harmful Drugs: Study Protocol for a Multiple Methods Design.
Peddie D; Small SS; Badke K; Wickham ME; Bailey C; Chruscicki A; Ackerley C; Balka E; Hohl CM
JMIR Res Protoc; 2016 Aug; 5(3):e169. PubMed ID: 27538362
[TBL] [Abstract][Full Text] [Related]
2. Pilot-testing an adverse drug event reporting form prior to its implementation in an electronic health record.
Chruscicki A; Badke K; Peddie D; Small S; Balka E; Hohl CM
Springerplus; 2016; 5(1):1764. PubMed ID: 27795906
[TBL] [Abstract][Full Text] [Related]
3. Adverse Drug Event Reporting From Clinical Care: Mixed-Methods Analysis for a Minimum Required Dataset.
Peddie D; Small SS; Badke K; Bailey C; Balka E; Hohl CM
JMIR Med Inform; 2018 Jun; 6(2):e10248. PubMed ID: 29954724
[TBL] [Abstract][Full Text] [Related]
4. Sharing Adverse Drug Event Reports Between Hospitals and Community Pharmacists to Inform Re-dispensing: An Analysis of Reports and Process Outcomes.
Cragg A; Small SS; Lau E; Rowe A; Lau A; Butcher K; Hohl CM
Drug Saf; 2023 Nov; 46(11):1161-1172. PubMed ID: 37783974
[TBL] [Abstract][Full Text] [Related]
5. Effectiveness of a computerized drug-monitoring program to detect and prevent adverse drug events and medication non-adherence in outpatient ambulatory care: study protocol of a randomized controlled trial.
Forster AJ; Erlanger TE; Jennings A; Auger C; Buckeridge D; van Walraven C; Tamblyn R
Trials; 2015 Jan; 16():2. PubMed ID: 25572800
[TBL] [Abstract][Full Text] [Related]
6. The patient experience of patient-centered communication with nurses in the hospital setting: a qualitative systematic review protocol.
Newell S; Jordan Z
JBI Database System Rev Implement Rep; 2015 Jan; 13(1):76-87. PubMed ID: 26447009
[TBL] [Abstract][Full Text] [Related]
7. Student and educator experiences of maternal-child simulation-based learning: a systematic review of qualitative evidence protocol.
MacKinnon K; Marcellus L; Rivers J; Gordon C; Ryan M; Butcher D
JBI Database System Rev Implement Rep; 2015 Jan; 13(1):14-26. PubMed ID: 26447004
[TBL] [Abstract][Full Text] [Related]
8. Why Clinicians Don't Report Adverse Drug Events: Qualitative Study.
Hohl CM; Small SS; Peddie D; Badke K; Bailey C; Balka E
JMIR Public Health Surveill; 2018 Feb; 4(1):e21. PubMed ID: 29487041
[TBL] [Abstract][Full Text] [Related]
9. Using ActionADE to create information continuity to reduce re-exposures to harmful medications: study protocol for a randomized controlled trial.
Hau JP; Brasher PMA; Cragg A; Small S; Wickham M; Hohl CM
Trials; 2021 Feb; 22(1):119. PubMed ID: 33546752
[TBL] [Abstract][Full Text] [Related]
10. Adverse drug event reporting systems: a systematic review.
Bailey C; Peddie D; Wickham ME; Badke K; Small SS; Doyle-Waters MM; Balka E; Hohl CM
Br J Clin Pharmacol; 2016 Jul; 82(1):17-29. PubMed ID: 27016266
[TBL] [Abstract][Full Text] [Related]
11. Characterizing and Comparing Adverse Drug Events Documented in 2 Spontaneous Reporting Systems in the Lower Mainland of British Columbia, Canada: Retrospective Observational Study.
Lau EY; Cragg A; Small SS; Butcher K; Hohl CM
JMIR Hum Factors; 2024 Jan; 11():e52495. PubMed ID: 38236629
[TBL] [Abstract][Full Text] [Related]
12. Perceived barriers to reporting adverse drug events in hospitals: a qualitative study using theoretical domains framework approach.
Mirbaha F; Shalviri G; Yazdizadeh B; Gholami K; Majdzadeh R
Implement Sci; 2015 Aug; 10():110. PubMed ID: 26250159
[TBL] [Abstract][Full Text] [Related]
13. Promoting and supporting self-management for adults living in the community with physical chronic illness: A systematic review of the effectiveness and meaningfulness of the patient-practitioner encounter.
Rees S; Williams A
JBI Libr Syst Rev; 2009; 7(13):492-582. PubMed ID: 27819974
[TBL] [Abstract][Full Text] [Related]
14. An external facilitation intervention to increase uptake of an adverse drug event reporting intervention.
Lau EY; Small SS; Butcher K; Cragg A; Loh GW; Shalansky S; Hohl CM
Front Health Serv; 2023; 3():1106586. PubMed ID: 37332530
[TBL] [Abstract][Full Text] [Related]
15. A Survey of Adverse Event Reporting Practices Among US Healthcare Professionals.
Stergiopoulos S; Brown CA; Felix T; Grampp G; Getz KA
Drug Saf; 2016 Nov; 39(11):1117-1127. PubMed ID: 27638657
[TBL] [Abstract][Full Text] [Related]
16. Automatic Detection of Adverse Drug Events in Geriatric Care: Study Proposal.
Gaspar F; Lutters M; Beeler PE; Lang PO; Burnand B; Rinaldi F; Lovis C; Csajka C; Le Pogam MA;
JMIR Res Protoc; 2022 Nov; 11(11):e40456. PubMed ID: 36378522
[TBL] [Abstract][Full Text] [Related]
17. Root Cause Analysis of Ambulatory Adverse Drug Events That Present to the Emergency Department.
Gertler SA; Coralic Z; López A; Stein JC; Sarkar U
J Patient Saf; 2016 Sep; 12(3):119-24. PubMed ID: 24583958
[TBL] [Abstract][Full Text] [Related]
18. Leveraging health information exchange to improve population health reporting processes: lessons in using a collaborative-participatory design process.
Revere D; Dixon BE; Hills R; Williams JL; Grannis SJ
EGEMS (Wash DC); 2014; 2(3):1082. PubMed ID: 25848615
[TBL] [Abstract][Full Text] [Related]
19. Development and Initial Validation of a Patient-Reported Adverse Drug Event Questionnaire.
de Vries ST; Mol PG; de Zeeuw D; Haaijer-Ruskamp FM; Denig P
Drug Saf; 2013 Sep; 36(9):765-77. PubMed ID: 23553447
[TBL] [Abstract][Full Text] [Related]
20. The Effectiveness of Integrated Care Pathways for Adults and Children in Health Care Settings: A Systematic Review.
Allen D; Gillen E; Rixson L
JBI Libr Syst Rev; 2009; 7(3):80-129. PubMed ID: 27820426
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]