This text will be of enormous value to anyone involved in the
monitoring and investigation of adverse medical events occurring
during the clinical trials, or during the post marketing period of
a drug. The book reviews the biochemical and physiological
abnormalities in each of the bodys organ systems and helps the
investigator decide if the problem is of drug-induced origin. Most
of the information is presented as a series of observations with
accompanying questions which should be addressed in order to make
an accurate diagnosis. Easy-to-read with useful flow charts for the
management of adverse drug events and examples of specific report
forms, this text will be of interest to all those involved in drug
monitoring in clinical medicine, pharmaceutical companies, contract
research organisations or regulatory authorities.
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