Construct and concurrent validity of a patient-reported adverse drug event questionnaire: a cross-sectional study

BACKGROUND: Direct patient-reported information about adverse drug events (ADEs) is important since it adds to healthcare professional-reported information about the safety of drugs. Previously, we developed an instrument to assess patient-reported ADEs in research settings. The aim of this study is...

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Detalles Bibliográficos
Autores principales: de Vries, Sieta T, Haaijer-Ruskamp, Flora M, de Zeeuw, Dick, Denig, Petra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243939/
https://www.ncbi.nlm.nih.gov/pubmed/25115618
http://dx.doi.org/10.1186/s12955-014-0103-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243939/
https://www.ncbi.nlm.nih.gov/pubmed/25115618
http://dx.doi.org/10.1186/s12955-014-0103-6

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