Using electronic medical record data to report laboratory adverse events

Despite the importance of adverse event (AE) reporting, AEs are under-reported on clinical trials. We hypothesized that electronic medical record (EMR) data can ascertain laboratory-based AEs more accurately than those ascertained manually. EMR data on 12 AEs for patients enrolled on two Children’s...

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Bibliografiset tiedot
Julkaisussa:Br J Haematol
Päätekijät: Miller, Tamara P., Li, Yimei, Getz, Kelly D., Dudley, Jesse, Burrows, Evanette, Pennington, Jeffrey, Ibrahimova, Azada, Fisher, Brian T., Bagatell, Rochelle, Seif, Alix E., Grundmeier, Robert, Aplenc, Richard
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2017
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5384859/
https://ncbi.nlm.nih.gov/pubmed/28146330
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bjh.14538
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