Pharmacokinetics of Ofloxacin and Levofloxacin for Prevention and Treatment of Multidrug-Resistant Tuberculosis in Children
Author(s) -
Stephanie Thee,
Anthony J. GarciaPrats,
Helen McIlleron,
Lubbe Wiesner,
Sandra Castel,
Jennifer Norman,
Heather R. Draper,
P L van der Merwe,
Anneke C. Hesseling,
H. Simon Schaaf
Publication year - 2014
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.02755-13
Subject(s) - ofloxacin , levofloxacin , pharmacokinetics , medicine , pharmacology , pharmacodynamics , tuberculosis , drug , antibiotics , antibacterial agent , oral administration , quinolone , ciprofloxacin , microbiology and biotechnology , biology , pathology
Limited data on fluoroquinolone pharmacokinetics and cardiac effects in children exist. Among 22 children receiving drug-resistant tuberculosis prophylaxis or treatment, serum concentrations following oral doses of levofloxacin (15 mg/kg of body weight) and ofloxacin (20 mg/kg) were lower than those expected from existing pediatric data, possibly due to differences in the formulations (crushed tablets). Drug exposures were lower than those in adults following standard doses and below the proposed pharmacodynamic targets, likely due to more rapid elimination in children. No QT prolongation was observed.
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