Analysis of data on spontaneous reports of adverse events associated with drugs
Some adverse drug reactions (ADRs) are not detected before marketing approval is given because clinical trials are not suited for their detection, for various reasons [5, 23]. Drug regulatory bodies therefore weigh the potential benefits of a drug against the harms and allow drugs to be marketed if...
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University of Glasgow
2014
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.591993 |