Abstract
For many drugs there is a high correlation between the concentration of drug in serum and clinical reponse. Optimal therapy with these drugs requires exceeding a minimal effective concentration (below which no adequate response is seen) while remaining below a maximal allowable concentration (above which drug toxicity becomes evident). Thus, a dose may be chosen quite rationally by the use of a desired serum concentration as the “therapeutic” end point. However, it is not possible to give the same dosage to all patients; a dose which proves effective in one patient will be ineffective in some and even toxic in others. This is because the dosage required to achieve serum concentrations within a certain, frequently narrow, range is confounded by variations in the way in which different individuals distribute and eliminate drugs.
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Reference
W.L. Chiou, M.A.F. Gadalla and G.W. Peng, Method for the rapid estimation of total body drug clearance and adjustment of dosage regimens in patients during a constant rate intravenous infusion, J. Pharmacokin. Biopharm. 6: 135–151 (1978).
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© 1984 Plenum Press, New York
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Muir, K.T. (1984). A General Method of Optimizing Individual Drug Dosage. In: Benet, L.Z., Levy, G., Ferraiolo, B.L. (eds) Pharmacokinetics. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2799-8_32
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DOI: https://doi.org/10.1007/978-1-4613-2799-8_32
Publisher Name: Springer, Boston, MA
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