Spontaneous Reporting Systems: Achieving Less Spontaneity and More Reporting

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Spontaneous Reporting Systems: Achieving Less Spontaneity and More Reporting

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dc.contributor.advisor Hutt, Peter Barton en_US
dc.contributor.author Berniker, Jessamyn S. en_US
dc.date.accessioned 2012-06-07T05:41:40Z
dc.date.issued 2001 en_US
dc.identifier.citation Spontaneous Reporting Systems: Achieving Less Spontaneity and More Reporting (2001 Third Year Paper) en
dc.identifier.uri http://nrs.harvard.edu/urn-3:HUL.InstRepos:8846816
dc.description.abstract The purpose of this article is to highlight and analyze possible improvements to spontaneous reporting systems, in particular, and drug safety, in general. Part I of this article will provide a background on adverse drug reactions and spontaneous reporting systems, with particular emphasis on the MedWatch reporting system currently used in the United States. Part II will discuss physician attitudinal studies performed worldwide that have attempted to highlight the reasons for the underreporting of adverse reactions and problems with reporting systems. Part III will analyze problems identified with spontaneous reporting systems and potential improvements of them. en
dc.language.iso en_US en
dash.license LAA en_US
dc.subject Food and Drug Law en
dc.subject drug safety en
dc.subject adverse drug reactions en
dc.subject MedWatch en
dc.subject spontaneous reporting systems en
dc.title Spontaneous Reporting Systems: Achieving Less Spontaneity and More Reporting en
dc.type Paper (for course/seminar/workshop) en_US
dc.date.available 2012-06-07T05:41:40Z

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