Sharing Adverse Drug Event Reports Between Hospitals and Community Pharmacists to Inform Re-dispensing: An Analysis of Reports and Process Outcomes

Author:

Cragg Amber,Small Serena S.,Lau Erica,Rowe Adrianna,Lau Anthony,Butcher Katherine,Hohl Corinne M.ORCID

Funder

Canadian Institutes of Health Research

Michael Smith Health Research BC

Ministry of Health, British Columbia

British Columbia SUPPORT Unit

Lower Mainland Consolidated Pharmacies

Vancouver Coastal Health Authority

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,Toxicology

Reference46 articles.

1. The WHO Research Priority Setting Working Group. Global priorities for research in patient safety (first edition) [Internet]. World Health Organization; 2008 [cited 2023 Sep 28]. https://www.who.int/publications/i/item/WHO-IER-PSP-2008.13

2. Harris Y, Hu DJ, Lee C, Mistry M, York A, Johnson TK. Advancing medication safety: establishing a national action plan for adverse drug event prevention. Jt Commun J Qual Patient Saf. 2015;41:351–60.

3. Hohl CM, Brubacher J, Hunte G, Wiens MO, Abu-Laban R, Singer J, et al. Clinical decision rules to improve the detection of adverse drug events in emergency department patients. Acad Emerg Med. 2012;19:640–9.

4. Hohl CM, Badke K, Zhao A, Wickham ME, Woo SA, Sivilotti MLA, et al. Prospective validation of clinical criteria to identify emergency department patients at high risk for adverse drug events. Griffey RT, editor. Acad Emerg Med. 2018;25:1015–26.

5. Zed PJ, Abu-Laban RB, Balen RM, Loewen PS, Hohl CM, Brubacher JR, et al. Incidence, severity and preventability of medication-related visits to the emergency department: a prospective study. Can Med Assoc J. 2008;178:1563–9.

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