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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Main Authors: Allen, Elizabeth N, Chandler, Clare IR, Mandimika, Nyaradzo, Pace, Cheryl, Mehta, Ushma, Barnes, Karen I
Formáid: Artigo
Teanga:Inglês
Foilsithe: BioMed Central 2013
Ábhair:
Methodology
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3848530/
https://ncbi.nlm.nih.gov/pubmed/24041367
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1475-2875-12-325
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