Hospital staff should use more than one method to detect adverse events and potential adverse events: incident reporting, pharmacist surveillance and local real-time record review may all have a place.
BACKGROUND: Over the past five years, in most hospitals in England and Wales, incident reporting has become well established but it remains unclear how well reports match clinical adverse events. International epidemiological studies of adverse events are based on retrospective, multi-hospital case...
Hoofdauteurs: | Olsen, S, Neale, G, Schwab, K, Psaila, B, Patel, T, Chapman, E, Vincent, C |
---|---|
Formaat: | Journal article |
Taal: | English |
Gepubliceerd in: |
2007
|
Gelijkaardige items
-
The reasons of the nursing staff to notify adverse events
door: Miriam Cristina Marques da Silva de Paiva, et al.
Gepubliceerd in: (2014-10-01) -
Role of the Clinical Pharmacist in Reducing Preventable Adverse Drug Events
door: Bahir A.Mshiemish
Gepubliceerd in: (2017-03-01) -
Postmarketing Surveillance of Full Spectrum Hemp Extract CBD Products: Reported Adverse Events and Serious Adverse Events
door: Colleen M. Kingsbury, et al.
Gepubliceerd in: (2024-09-01) -
In light of recent events, we may have to see adverse effect profile in new perspective
door: Sahjid Mukhida, et al.
Gepubliceerd in: (2024-11-01) -
Internal Strengths for Adverse Life Events
door: Jian Zhao, et al.
Gepubliceerd in: (2024-08-01)