Cargando…
Completeness of adverse drug reactions reports of the Saudi adverse event reporting system
OBJECTIVES: To assess completeness of reports in the Saudi Adverse Event Reporting System (SAERS), which is a part of the Saudi Food and Drug Authority pharmacovigilance system for monitoring the safety of medications. METHODS: A cross-sectional study was conducted in Riyadh, Saudi Arabia using the...
Autores principales: | Alshammari, Thamir M., Al-Kathiri, Wa’ad H., Louet, Hervé Le, Aljadhey, Hisham S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Saudi Medical Journal
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503901/ https://www.ncbi.nlm.nih.gov/pubmed/26108586 http://dx.doi.org/10.15537/smj.2015.7.11751 |
Ejemplares similares
-
Public awareness and perception toward Adverse Drug Reactions reporting in Riyadh, Saudi Arabia
por: Sales, Ibrahim, et al.
Publicado: (2017) -
A qualitative exploration of the major challenges facing pharmacovigilance in Saudi Arabia
por: Aljadhey, Hisham, et al.
Publicado: (2015) -
Pharmacovigilance system in Saudi Arabia
por: Alshammari, Thamir M., et al.
Publicado: (2017) -
Signals of bleeding among direct-acting oral anticoagulant users compared to those among warfarin users: analyses of the post-marketing FDA Adverse Event Reporting System (FAERS) database, 2010–2015
por: Alshammari, Thamir M, et al.
Publicado: (2018) -
Knowledge, attitudes & practices of healthcare professionals in hospitals towards the reporting of adverse drug reactions in Saudi Arabia: A multi-centre cross sectional study
por: AlShammari, Thamir M., et al.
Publicado: (2018)