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% File nlme/man/Quinidine.Rd% Part of the nlme package for R% Distributed under GPL 2 or later: see nlme/LICENCE.note\name{Quinidine}\alias{Quinidine}\title{Quinidine Kinetics}\description{The \code{Quinidine} data frame has 1471 rows and 14 columns.}\format{This data frame contains the following columns:\describe{\item{Subject}{a factor identifying the patient on whom the data were collected.}\item{time}{a numeric vector giving the time (hr) at which the drug wasadministered or the blood sample drawn. This is measuredfrom the time the patient entered the study.}\item{conc}{a numeric vector giving the serum quinidine concentration (mg/L).}\item{dose}{a numeric vector giving the dose of drug administered (mg).Although there were two different forms of quinidineadministered, the doses were adjusted for differences insalt content by conversion to milligrams of quinidine base.}\item{interval}{a numeric vector giving the when the drug has been given atregular intervals for a sufficiently long period of time toassume steady state behavior, the interval is recorded.}\item{Age}{a numeric vector giving the age of the subject on entry tothe study (yr).}\item{Height}{a numeric vector giving the height of the subject on entryto the study (in.).}\item{Weight}{a numeric vector giving the body weight of the subject (kg).}\item{Race}{a factor with levels\code{Caucasian},\code{Latin}, and\code{Black} identifying the race of the subject.}\item{Smoke}{a factor with levels\code{no} and\code{yes} giving smoking status at the time of themeasurement.}\item{Ethanol}{a factor with levels\code{none},\code{current},\code{former} giving ethanol (alcohol) abuse status at thetime of the measurement.}\item{Heart}{a factor with levels\code{No/Mild},\code{Moderate}, and\code{Severe} indicating congestive heart failure for the subject.}\item{Creatinine}{an ordered factor with levels\code{< 50} < \code{>= 50} indicating the creatinine clearance (mg/min).}\item{glyco}{a numeric vector giving the alpha-1 acid glycoproteinconcentration (mg/dL). Often measured at the same time asthe quinidine concentration.}}}\details{Verme et al. (1992) analyze routine clinical data onpatients receiving the drug quinidine as a treatment for cardiacarrhythmia (atrial fibrillation or ventricular arrhythmias). Allpatients were receiving oral quinidine doses. At irregular intervalsblood samples were drawn and serum concentrations of quinidine weredetermined. These data areanalyzed in several publications, including Davidian and Giltinan (1995,section 9.3).}\source{Pinheiro, J. C. and Bates, D. M. (2000), \emph{Mixed-Effects Models in Sand S-PLUS}, Springer, New York. (Appendix A.25)Davidian, M. and Giltinan, D. M. (1995), \emph{Nonlinear Models forRepeated Measurement Data}, Chapman and Hall, London.Verme, C. N., Ludden, T. M., Clementi, W. A. and Harris,S. C. (1992), Pharmacokinetics of quinidine in male patients: Apopulation analysis, \emph{Clinical Pharmacokinetics}, \bold{22},468-480.}%\examples{}\keyword{datasets}