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Review of Reported Clinical Information System Adverse Events in US Food and Drug Administration Databases
BACKGROUND: The US FDA has been collecting information on medical devices involved in significant adverse advents since 1984. These reports have been used by researchers to advise clinicians on potential risks and complications of using these devices. OBJECTIVE: Research adverse events related to th...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Schattauer
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3175794/ https://ncbi.nlm.nih.gov/pubmed/21938265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4338/ACI-2010-11-RA-0064 |
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