Single-dose pharmacokinetics of thalidomide in human immunodeficiency virus-infected patients
Author(s) -
Stephen C. Piscitelli,
William D. Figg,
Beatrice H. Hahn,
Gerald D. Kelly,
Steve D. Thomas,
Robert Walker
Publication year - 1997
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.41.12.2797
Subject(s) - pharmacokinetics , thalidomide , dosing , adverse effect , medicine , pharmacology , human immunodeficiency virus (hiv) , sida , viral disease , gastroenterology , virology , multiple myeloma
The pharmacokinetics of thalidomide in nine human immunodeficiency virus-infected patients were studied. Single doses of thalidomide were well absorbed, with mean peak concentrations (+/- standard deviations) of 1.17 +/- 0.21 and 3.47 +/- 1.14 microg/ml in the 100- and 300-mg dosing groups, respectively, and the mean elimination half-life was approximately 6 h. Adverse effects were mild, with drowsiness being reported for seven of nine patients.
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