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Ceftibuten and bactericidal kinetics. Comparative in vitro activity against Enterobacteriaceae producing extended
1Max von Pettenkofer Institute, Munich, Federal Republic of Germany.
Diagnostic Microbiology and Infectious Disease
|January 1, 1991
Abstract:
Ceftibuten, compared to cefixime, cefetamet, cefpodoxime, loracarbef, cefprozil, cefuroxime, cefaclor, and cefadroxil, was the most active oral cephalosporin derivative against Enterobacteriaceae producing plasmid-encoded broad spectrum beta-lactamases. In a pharmacodynamic model, ceftibuten was bactericidal for Haemophilus influenzae and Streptococcus pneumoniae at concentrations simulating human serum levels following 200 mg, p.o., b.i.d.