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Experimental Pharmacology and Toxicology of Antituberculosis Drugs

  • Chapter
Antituberculosis Drugs

Part of the book series: Handbook of Experimental Pharmacology ((HEP,volume 84))

Abstract

The anti-tuberculosis agents are, chemically, a very heterogeneous group exhibiting a wide spectrum of pharmacological and toxicological effects on the various organ systems. These range from the very early recognized ototoxicity and nephrotoxicity of the aminoglycosides, to the question of neurotoxicity, carcinogenicity and mutagenicity of INH, to the oculotoxicity of ethambutol and to effects on neuro-muscular transmission of the aminoglycosides. Whilst for some substances there are enormous numbers of publications, there are other substances where there is a noticeable lack of published pharmacological and toxicological data. With regard to the latter substances it was possible, in some cases, to include in this review previously unpublished results of studies carried out by the manufacturing companies. Since most of the anti-tuberculosis agents were introduced 20 years–30 years ago, it is practically impossible to assess the old publications on the basis of modern standards. It would be misguided, however, to ignore the results of the early studies since they provided important basic data.

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Tettenborn, D. (1988). Experimental Pharmacology and Toxicology of Antituberculosis Drugs. In: Bartmann, K. (eds) Antituberculosis Drugs. Handbook of Experimental Pharmacology, vol 84. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-72873-0_5

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