In a multicenter study, the MICs of FK-037 for 90%o of the strains tested (MIC90s) were <1 ,ug/ml for members of the family Enterobacteriaceae other than Citrobacter freundii, Enterobacter spp., and Serratia marcescens. Activity against Pseudomonas aeruginosa was variable, with a MIC50 and a MIC,0 of 4 and 32 ,ug/ml, respectively. Relative to cefepime, however, FK-037 was less active against ceftazidime-resistant isolates of Enterobacter cloacae. The MIC,0 of FK-037 for methicillin-resistant staphylococci was >16 ,ug/ml.FK-037 is a novel injectable oxime-type cephalosporin antibiotic with a 1-hydroxyethyl-5-aminopyrazole moiety at the three position (15). Data presented in abstracts in 1991 and 1992 suggested that FK-037 was more active than currently available extended-spectrum cephalosporins against staphylococci, including methicillin-resistant strains (5,12,15); however, at four times its MIC, FK-037 reduced the number of CFU of methicillin-resistant Staphylococcus aureus by only 1 order of magnitude while vancomycin reduced the number of CFU by over 3 orders of magnitude in killing curve studies (1). In studies by Neu et al. (14), 16 ,ug of FK-037 per ml inhibited 50% of the S. aureus isolates tested with oxacillin MICs of >16 ,ug/ml. FK-037 has also been reported to have a broad spectrum of activity against gram-negative bacilli, including members of the family Enterobacteriaceae and Pseudomonas aeruginosa, and to be active against many ceftazidime-resistant isolates of Citrobacter spp., Enterobacter spp., and P. aeruginosa (2, 4-7, 11, 13, 16