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Effect of severe renal impairment on the pharmacokinetics of azimilide following single dose oral administration

AIMS: To assess the influence of severe renal impairment on azimilide pharmacokinetics. METHODS: A single oral dose of 125 mg azimilide dihydrochloride was administered to subjects with normal and severely impaired renal function. Blood and urine samples were collected for 22–28 and 10 days, respect...

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Bibliografiske detaljer
Main Authors: Corey, Alfred E, Agnew, Jeffrey R, Valentine, Suzanne N, Parekh, Nikhil J, Powell, James H, Thompson, Gary A
Format: Artigo
Sprog:Inglês
Udgivet: Blackwell Science Inc 2002
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1874454/
https://ncbi.nlm.nih.gov/pubmed/12445022
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2125.2002.01664.x
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