Evaluating harm associated with anti-malarial drugs: a survey of methods used by clinical researchers to elicit, assess and record participant-reported adverse events and related data

BACKGROUND: Participant reports of medical histories, adverse events (AE) and non-study drugs are integral to evaluating harm in clinical research. However, interpreting or synthesizing results is complicated if studies use different methods for ascertaining and assessing these data. To explore how...

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Detalles Bibliográficos
Autores principales: Allen, Elizabeth N, Chandler, Clare IR, Mandimika, Nyaradzo, Pace, Cheryl, Mehta, Ushma, Barnes, Karen I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848530/
https://www.ncbi.nlm.nih.gov/pubmed/24041367
http://dx.doi.org/10.1186/1475-2875-12-325

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848530/
https://www.ncbi.nlm.nih.gov/pubmed/24041367
http://dx.doi.org/10.1186/1475-2875-12-325

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