Opportunities for selective reporting of harms in randomized clinical trials: Selection criteria for non-systematic adverse events

BACKGROUND: Adverse events (AEs) in clinical trials may be reported in multiple sources. Different methods for reporting adverse events across trials or across sources for a single trial may produce inconsistent information about the adverse events associated with interventions. METHODS: We compared...

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Detalles Bibliográficos
Autores principales: Mayo-Wilson, Evan, Fusco, Nicole, Hong, Hwanhee, Li, Tianjing, Canner, Joseph K., Dickersin, Kay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6728982/
https://www.ncbi.nlm.nih.gov/pubmed/31488200
http://dx.doi.org/10.1186/s13063-019-3581-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6728982/
https://www.ncbi.nlm.nih.gov/pubmed/31488200
http://dx.doi.org/10.1186/s13063-019-3581-3

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