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How Should Long-Term Safety of a New Antiarrhythmic Drug Be Determined?

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The Evaluation of New Antiarrhythmic Drugs

Part of the book series: Developments in Cardiovascular Medicine ((DICM,volume 11))

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Abstract

During previous portions of this symposium, much useful information has been presented regarding the electrophysiology of ischemia and of antiarrhythmic drugs. One might characterize what is known about the “electrophysiology” of postmarketing drug surveillance as follows: it is fragmented, abberant and ectopic. A recent report of a United States Senate Committee advocating improved postmarketing drug surveillance echoes similar pleas from the past.1,2

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References

  1. Culliton BJ and Waterfall WK. Post-marketing surveillance. Br Med J 280: 1175–6, 1980.

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  2. Wilson AB. Post-marketing surveillance of adverse reactions to new medicines. Br Med J 2: 1001–3, 1977.

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© 1981 Martinus Nijhojf Publishers bv, The Hague.

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Karliner, J.S. (1981). How Should Long-Term Safety of a New Antiarrhythmic Drug Be Determined?. In: Morganroth, J., Moore, E.N., Dreifus, L.S., Michelson, E.L. (eds) The Evaluation of New Antiarrhythmic Drugs. Developments in Cardiovascular Medicine, vol 11. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-8270-3_21

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  • DOI: https://doi.org/10.1007/978-94-009-8270-3_21

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-009-8272-7

  • Online ISBN: 978-94-009-8270-3

  • eBook Packages: Springer Book Archive

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