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The risk determined from PMS studies

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Medicines and Risk/Benefit Decisions

Part of the book series: CMR Workshop Series ((CMRWS))

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Abstract

In animal studies or in controlled clinical trials, investigators are looking for common beneficial or adverse outcomes. With these studies there is a relatively small number of factors which are likely to change at any one time. Mostly these are known and can be measured. Moreover, in most instances the time scales between first exposure and termination of the experiment are short, thus minimizing the period during which intervening variables can exercise a major effect on the study outcome. Indeed when we look at examples of trials in which there is a long delay between entry and end-point, we often find ourselves in areas of major controversy as regards the interpretations of the data - a situation not entirely dissimilar to that pertaining to most observational studies to date.

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References

  1. Colin-Jones, D.G., Langman, M.J.S., Vessey, M.P. and Lawson, D.H. (1982). Cimetidine and gastric cancer: preliminary report from post-marketing surveillance study. Br. Med. J., 285, 1311

    Article  CAS  Google Scholar 

  2. Colin-Jones, D.G., Langman, M.J.S., Vessey, M.P. and Lawson, D.H. (1983). Postmarketing surveillance of the safety of cimetidine: 12 month mortality report. Br. Med. J., 286, 1713

    Article  CAS  Google Scholar 

  3. Colin-Jones, D.G., Langman, M.J.S., Vessey, M.P. and Lawson, D.H. Post-marketing surveillance of the safety of cimetidine: 12 month morbidity report. Q.J. Med., 54, 215–253

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© 1987 MTP Press Limited

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Lawson, D.H. (1987). The risk determined from PMS studies. In: Walker, S.R., Asscher, A.W. (eds) Medicines and Risk/Benefit Decisions. CMR Workshop Series. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-3221-0_7

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  • DOI: https://doi.org/10.1007/978-94-009-3221-0_7

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-7946-4

  • Online ISBN: 978-94-009-3221-0

  • eBook Packages: Springer Book Archive

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