Underreporting of adverse events to health authorities by healthcare professionals: a red flag-raising descriptive study

Underreporting of adverse events to health authorities by healthcare professionals: a red flag-raising descriptive study

An adverse event (AE) is any undesirable medical manifestation in an individual who has received pharmacological treatment. To be considered serious (SAE), it needs to meet minimally one of the severity criteria by Health Canada. The most recent data (2006) suggested that AEs were underreported (

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Veröffentlicht in:International journal for quality in health care 2024-12, Vol.36 (4)
Hauptverfasser: Lavallée, Maude, Corbin, Sonia, Pradhan, Pallavi, Guefack, Laura Blonde, Thibault, Magalie, Méthot, Julie, Bérard, Anick, Piché, Marie-Eve, Gimenes, Fernanda Raphael Escobar, Darveau, Rosalie, Cloutier, Isabelle, Leclerc, Jacinthe
Format: Artikel
Sprache:eng
Schlagworte:
Adult
Adverse Drug Reaction Reporting Systems - statistics & numerical data
Aged
Aged, 80 and over
Canada - epidemiology
Drug-Related Side Effects and Adverse Reactions - epidemiology
Female
Health Personnel - statistics & numerical data
Humans
Incidence
Male
Mandatory Reporting
Middle Aged
Quebec - epidemiology
Retrospective Studies
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Beschreibung
Zusammenfassung:An adverse event (AE) is any undesirable medical manifestation in an individual who has received pharmacological treatment. To be considered serious (SAE), it needs to meet minimally one of the severity criteria by Health Canada. The most recent data (2006) suggested that AEs were underreported (
ISSN:1353-4505
1464-3677
1464-3677
DOI:10.1093/intqhc/mzae109