Applied Clinical Informatics Article
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 the use of Clinical Information Systems (CIS) as reported in FDA databases. METHODS: Three large, national, adverse event medical device databases were examined for reports pertaining to [...]
Author(s): Myers, Risa B, Jones, Stephen L, Sittig, Dean F
DOI: 10.4338/ACI-2010-11-RA-0064