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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2019
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| Materias: | |
| 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 |