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...

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Detalles Bibliográficos
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:
Original Article
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

Internet

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

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