Murray P R, Jones R N, Washington J A, Gerlach E H, Allen S D
Department of Pathology, Washington University Medical Center, St. Louis, Missouri.
Diagn Microbiol Infect Dis. 1993 Nov-Dec;17(4):307-11. doi: 10.1016/0732-8893(93)90040-e.
The in vitro activity of E4868 was compared with that of ciprofloxacin and temafloxacin in a multicenter study. More than 90% of Enterobacteriaceae and 82% of the 651 isolates of Pseudomonas aeruginosa, as well as > 95% of the oxacillin-susceptible staphylococci, 100% of the beta-hemolytic streptococci, and 76% of the enterococcal isolates were susceptible to E4868 (minimum inhibitory concentrations, < or = 2 micrograms/ml). E4868 was generally equivalent or slightly less active than ciprofloxacin against the Enterobacteriaceae and Pseudomonas and more active against staphylococci and beta-hemolytic streptococci. The activity of E4868 was generally equivalent to or slightly greater than that of temafloxacin against all major groups of organisms.