TY - JOUR
T1 - Bacteriological and clinical studies on FK037
AU - Sawae, Yoshiro
AU - Okada, Kaoru
AU - Shimono, Nobuyuki
AU - Misumi, Hiroyasu
AU - Eguchi, Katsuhiko
AU - Niho, Yoshiyuki
AU - Takaki, Koji
PY - 1994
Y1 - 1994
N2 - We performed bacteriological and clinical studies on FK037, a new parenteral cephalosporin antibiotic, with the following results. 1) Antimicrobial activity The MIC90 of FK037 against various clinical isolates (10 species, 238 strains) was as follows: 3.13 μg/ml against methicillin-sensitive Staphylococcus aureus, 50 μg/ml against methicillin-resistant S. aureus (MRSA), >100 μg/ml against Enterococcus faecalis, 0.10μg/ml against Escherichia coli, ≦ 0.05 μg/ml against Klebsiella pneumoniae, 3.13 μg/ml against Enterobacter cloacae, 1.56 μg/ml against Enterobacter aerogenes, 3.13 μg/ml against Citrobacter freundii, ≦0.05 μg/ml against Proteus mirabilis, 0.10 μg/ml against Proteus vulgaris, 25μg/ml against Pseudomonas aeruginosa. Its activity against these bacterial species including MRSA was more potent than that of control drugs; ceftazidime (CAZ), flomoxef (FM0X), ceftizoxime (CZX) and cefotiam (CTM). The activity against P. aeruginosa was almost as potent as that of CAZ. The activity against E. faecalis was less active as well as that of the control drugs. 2) Clinical efficacy Four patients with pneumonia were treated with FK037 at daily doses of 1.0 or 4.0 g for 7~14 days. Clinical response was excellent in 3 patients and good in 1. No adverse reactions or abnormal laboratory findings were observed.
AB - We performed bacteriological and clinical studies on FK037, a new parenteral cephalosporin antibiotic, with the following results. 1) Antimicrobial activity The MIC90 of FK037 against various clinical isolates (10 species, 238 strains) was as follows: 3.13 μg/ml against methicillin-sensitive Staphylococcus aureus, 50 μg/ml against methicillin-resistant S. aureus (MRSA), >100 μg/ml against Enterococcus faecalis, 0.10μg/ml against Escherichia coli, ≦ 0.05 μg/ml against Klebsiella pneumoniae, 3.13 μg/ml against Enterobacter cloacae, 1.56 μg/ml against Enterobacter aerogenes, 3.13 μg/ml against Citrobacter freundii, ≦0.05 μg/ml against Proteus mirabilis, 0.10 μg/ml against Proteus vulgaris, 25μg/ml against Pseudomonas aeruginosa. Its activity against these bacterial species including MRSA was more potent than that of control drugs; ceftazidime (CAZ), flomoxef (FM0X), ceftizoxime (CZX) and cefotiam (CTM). The activity against P. aeruginosa was almost as potent as that of CAZ. The activity against E. faecalis was less active as well as that of the control drugs. 2) Clinical efficacy Four patients with pneumonia were treated with FK037 at daily doses of 1.0 or 4.0 g for 7~14 days. Clinical response was excellent in 3 patients and good in 1. No adverse reactions or abnormal laboratory findings were observed.
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U2 - 10.11250/chemotherapy1953.42.Supplement3_196
DO - 10.11250/chemotherapy1953.42.Supplement3_196
M3 - Article
AN - SCOPUS:0028036573
SN - 0009-3165
VL - 42
SP - 196
EP - 201
JO - Chemotherapy
JF - Chemotherapy
ER -