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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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| Publicat a: | Br J Haematol |
|---|---|
| Autors principals: | , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2017
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| Matèries: | |
| Accés en línia: | 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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