Staphylococcus sp. K.pneumoniae P.mirabilis C.freundii E. cloacae Serratia sp. P. aeruginosa ml, Enterococcus avium >100ƒÊg/ml
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1 CHEMOTHERAPY SEPT cefoperazone ceftazidime (CAZ), imipenem (IPM) Staphylococcus sp., Enterococcus (CPZ), faecalis, Escherichia coli, Klebsiella pneumoniae, Citrobacter freundii, Enterobacter cloacae, Serratia sp., Proteus mirabilis, Proteus vulgaris, Pseudomonas aeruginosa Serratia marcescens, Pseudomonas aeruginosa phylococcus sp., Enterococcus faecalis, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Proteus vulgaris, Enterobacter cloacae, Citrobacter P.aeruginosa, Acinetobacter calcoa- Enterobacter sp., Citrobacter sp. freundii, Serratia sp., P.aeruj inosa
2 Staphylococcus sp. K.pneumoniae P.mirabilis C.freundii E. cloacae Serratia sp. P. aeruginosa ml, Enterococcus avium >100ƒÊg/ml
3 CHEMOTHERAPY Table 1. In vitro antibacterial activity of cefclidin against clinical isolates Inoculum size: 106 CFU/ml
4 VOL.40 S-4 Table 2. Clinical summary of complicated UTI patients treated with cefclidin CCP: chronic complicated pyelonephritis CCC: chronic complicated cystitis VUR: vesicoureteral reflex HAM: HTL V-1 associated myelopathy * before treatment after treatment ** UTI: criteria proposed by the UTI Committee Dr.: Dr's evaluation
5 CHEMOTHERAPY SEPT Table 3. Overall clinical efficacy of cefclidin in complicated UTI Bacteriological response * regardless of bacterial count Table 4. Overall clinical efficacy of cefclidin classified by the type of infection K.pneumoniae, C.freundii, E. cloacae, P. aeruginosa
6 Table 5. Bacteriological response to cefclidin in complicated UTI *regardless of bacterial count Table 6. Strains*appearing after cefclidin treatment in complicated UTI *regardless of bacterial count YLO: yeast like organism
7 CHEMOTHERAPY Table 7. Relation between MIC and bacteriological response to cefclidin treatment in complicated UTI No. of strains eradicated/no. of strains isolated Table 8. Changes in laboratory test results 8) Collatz E et al: Developement of resistance to 3) Watanabe N, Katsu K, Moriyama M, and Kitoh K: In vitro evaluation of E1040, a new cephalosporin with potent antipseudomonal activity. Antimicrob Agent Chemother 32: 693 `701, ) Spratt BG, Pardee AB: Penicillin bin ding protein and cell shape in E.coli. Nature 254: 516,1975 beta-lactam antibiotics with specific referens to third generation cephalosporins. Antimicrob Chemother 14 (B): 13,1984
8 VOL.40 S-4 9) Yokota T: Methicillin and cephemresistant Staphylococcus aureus. Infect Inflam Immun 14: 87,1984 ANTIMICROBIAL ACTIVITIES AND CLINICAL STUDIES ON CEFCLIDIN IN COMPLICATED URINARY TRACT INFECTION Kazuya Kawahara, Motoshi Kawahara, Yoshihiro Mizuma, Shinichi Makinose Toshihiro Gotou, Nichiro Sakamoto and Yoshitada Ohi Department of Urology, Faculty of Medicine, Kagoshima University , Sakuragaoka, Kagoshima 890, Japan Antimicrobial activities and clinical studies on cefclidin (CFCL), a new injectable cephalosporin, were performed and the following results were obtained. 1. Antibacterial activity of cefclidin Antibacterial activity of CFCL against 10 kinds of urinary pathogenic bacteria consisting of each 30 strains from urine were studied and compared to cefoperazone (CPZ), ceftazidime (CAZ) and imipenem(ipm). As to the antibacterial activities against Escherichia coli, Klebsiella pneumoniae, Citrobacter freundii, Enterobacter cloacae and Pseudomonas aeruginosa, CFCL was superior to the other drugs. Against Proteus mirabilis and Proteus vulgaris, CFCL showed weaker activities than CAZ, but stronger activities than both IPM and CPZ. Antibacterial activity of CFCL was inferior to CAZ and IPM against Serratia marcescens. 2. Clinical efficacy CFCL was administered in a daily dose of 1.0g or 2.0g for five consecutive days to 15 cases by i. v. or drip infusion. The overall clinical efficacy rate was 86.7% (13/15). 3. Bacteriological response 22 of 23 strains (95.7%) isolated from patients with urinary tract infection including 5 of Grampositive cocci and Gram-negative rods were eradicated. 4. Adverse reaction No severe adverse reactions and abnormal laboratory findings or ophthalmologic disorders was observed.
epidermidis, Enterococcus faecalis, Enterococcus Klebsiella pneumoniae, Proteus mirabilis, indolepositive Proteus spp., Enterobacter spp., Serratia
epidermidis, Enterococcus faecalis, Enterococcus Klebsiella pneumoniae, Proteus mirabilis, indolepositive Proteus spp., Enterobacter spp., Serratia Table 3. Overall clinical efficacy of cefozopran in
Fig.2. Sensitivity distribution of clinical isolates of S. epidermidis (24 strains, 106 CFU/ml) Staphylococcus aureus Staphylococcus epider- midis Ent
Fig.2. Sensitivity distribution of clinical isolates of S. epidermidis (24 strains, 106 CFU/ml) Staphylococcus aureus Staphylococcus epider- midis Enterococcus faecalis Klebsiella pneumoniae, Morganella
CHEMOTHERAPY JUN Citrobacter freundii 27, Enterobacter aerogenes 26, Enterobacter cloacae 27, Proteus rettgeri 7, Proteus inconstans 20, Proteus
VOL. 32 S-4 CHEMOTHERAPY Fig. 1 Chemical structure of sodium cefoperazone Fig. 2 Chemical structure of sodium cefoperazone CHEMOTHERAPY JUN. 1984 Citrobacter freundii 27, Enterobacter aerogenes 26, Enterobacter
Key words : 7432-S, Oral cephem, Urinary tract infection Fig. 1. Chemical structure of 7432-S.
Key words : 7432-S, Oral cephem, Urinary tract infection Fig. 1. Chemical structure of 7432-S. Table 1. Clinical summary of acute uncomplicated cystitis patients treated with 7432-S UTI : Criteria by the
Table 1. Antibacterial spectrum SBT ABPC ABPC CPZ : sulbactamiampicillin : ampicillin : cefoperazone
Table 1. Antibacterial spectrum SBT ABPC ABPC CPZ : sulbactamiampicillin : ampicillin : cefoperazone (inoculum size= 106 CFU/ml) (Ĉ-lactamase producer : 2 strains) Fig. 1. Sensitivity distribution of
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Fig. 1 Chemical structure of KW-1070
Fig. 1 Chemical structure of KW-1070 Fig. 2 Sensitivity distribution of clinical isolates Fig. 4 Sensitivity distribution of clinical isolates Fig. 3 Sensitivity distribution of clinical isolates Fig.
CHEMOTHERAPY Proteus mirabilis GN-79 Escherichia coli No. 35 Proteus vulgaris GN-76 Pseudomonas aeruginosa No. 11 Escherichia coli ML-1410 RGN-823 Kle
VOL. 29 NO.8 CHEMOTHERAPY 865 CHEMOTHERAPY Proteus mirabilis GN-79 Escherichia coli No. 35 Proteus vulgaris GN-76 Pseudomonas aeruginosa No. 11 Escherichia coli ML-1410 RGN-823 Klebsiella pneumoniae GN-69
Fig. 1 Chemical structure of DL-8280
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Table 1. Influence of urine ph on MBCs of new quinolones against Escherichia coli NIHJ JC-2 and Pseudomonas aeruginosa 18S; MBCs in urine were compared with those in Miieller-Hinton broth. Table 2. Influence
Table 1. Antibacterial activitiy of grepafloxacin and other antibiotics against clinical isolates
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VOL.39 S-1 CHEMOTHERAPY FEB. 1981 Table 1. Activity of cefpirome and others against clinical isolates VOL.39 S-1 CHEMOTHERAPY FEB. 1991 72 M, 55.5 kg 66 F, 53 kg Chronic bronchitis Bronchopneumonia Peak
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Table1MIC of BAY o 9867 against standard strains
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366 12 THE JAPANESE JOURNAL OF ANTIBIOTICS 65 6 Dec. 2012 1 8 DNA 2,3 16 12 20 171 2008 12 2010 11 2 3,558 4.44% 1.65% 1.17% 90% 9 Escherichia coli -
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β Moraxella catarrhalis Escherichia coli Citrobacter Klebsiella pneumoniae Enterobacter cloacae Serratia marcescens Proteus Pseudomonas aeruginosa Acinetobacter Bacteroides fragilis β Haemophilus influenzae
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988 CHEMOTHERAPY NOV. 1971
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Table 1 Antibacterial spectra of CPM and other antimicrobials against anaerobes Fig. 1 In vitro activity of CPM and other antibiotics against B. fragilis (136 strains) Fig. 2 In vitro activity of CPM and
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VOL.32 S-9 CHEMOTHERAPY Table 1 Minimum inhibitory concentrations of AC-1370, CPZ and CAZ Table 2 Efficacy of AC-1370 and CPZ against systemic infections in mice *Inoculum size: 106 cells/ml * 95% confidence
Table 1 Survival rates of infected mice given antibiotic doses producing peak serum a) S. aurcus Smith Challenge dose :7 ~10 (5% mucin) CFU/mouse. LD50: 1 ~103 (5% mucin) CFU/mouse. Table 2 Survival rates
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Table 1.Concentration of gatifloxacin (Middle-ear) Table 2.Concentration of gatifloxacin (Paranasal sinuses) Table 3.Concentration of gatifloxacin (Tonsil) Table 4.No.of patients studied Table 5.Background
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VOL. 30 S-3 CHEMOTHERAPY imeumoniae, Serratia marcescens, Proteus sp, CHEMOTHERAPY DEC. 1982 Table 1 Antibacterial spectra of T-1982, CTT, CMZ, CTX, CPZ and CEZ 106 CFU/ml Note: P; Peptococcus, S; Streptococcus,
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Clostridium difficile ciprofloxacin, ofloxacin, norfloxacin Bifidobacterium Lactobacillus Lactobacillus Bacteroides fragilis B. fragilis C. difficile
Clostridium difficile ciprofloxacin, ofloxacin, norfloxacin Bifidobacterium Lactobacillus Lactobacillus Bacteroides fragilis B. fragilis C. difficile Key words: temafloxacin, TA-167, Bacteroides fragilis,
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- 1 - - 1 - ... 1... 2... 4... 5... 9... 11... 14... 16... 20... 21... 22... 23... 23 - 1 - - 2 - - 3 - - 4 - - 5 - - 6 - - 7 - - 8 - - 9 - ( ) - 10 - - 11 - Pseudomonas aeruginosa Escherichia coli Staphylococcus
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Key words : R-plasmid, Urinary tract infection, E. coli Fig. 1. MIC distribution against E. coli isolated from urinary tract (366 strains) and isolation - frequencies of drug-resistant strains Table 1.
Table 1 Classification of female patients with vealcal irritating symptom by their signs Urination pain with other vesical irritability or not Table 2 Serum levels of DL-8280 after a single oral administration
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2108 CHEMOTHERAPY SEPT Table 1 Antimicrobial spectrum Fig. 1
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Escherichia coli Enterococcus faecalisstreptococcus agalactiae Klebsiella pneumoniae Staphylococcus epidermidis E. colie. faecalispseudomonas aeruginosa K. pneumoniae S. agalactiae E. coli E. coli μ p
Table 1.Quality control of MICs for reference strains Table 2.Antimicrobial activity of gatifloxacin against aerobic bacteria Table 4.Antimicrobial activity of gatifloxacin and other quinolones against
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R06_01
Staphylococcus aureus (MSSA) PCG (N=118,334) 57,369 (48.5%) 判定不能 :3 (0.0%) 60,962 (51.5%) CEZ (N=143,723) I:42 (0.0%) 143,635 (99.9%) R:46 (0.0%) CVA/AMPC (N=19,281) R:14 (0.1%) 19,265 (99.9%) 判定不能 :2
日本化学療法学会雑誌第53巻第S-3号
moxifloxacin in vitro moxifloxacin in vitro 17 9 6 17 11 21 moxifloxacinmflx in vitro cefdinir CFDNclavulanic acidamoxicillincvaampcclarithromycincamclindamycincldm levofloxacinlvfx 1MFLX Clostridium clostridiiformeclostridium
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53-0115-00-4PDF 53-0115-00-4PDF INDEX 1 3 9 11 12 16 21 38 39 40 42 43 44 45 46 47 53-0115-00-4PDF 3 1 Critical Semicritical Noncritical Disinfection Sterilization 53-0115-00-4PDF 2 53-0115-00-4PDF O =
2 CHEMOTHERAPY JAN. 1976 VOL. 24 NO. 1 CHEMOTHERAPY 3 Table 1 Antibacterial spectra of Cephacetrile, Cephalothin, Cephaloridine and Cefazolin 4 CHEMOTHERAPY JAN. 1976 Fig. 1 In vitro activity of Cephacetrile,
400 46 THE JAPANESE JOURNAL OF ANTIBIOTICS 65 6 Dec. 2012 LVFX 100 mg 3 / 7 150 mg 2 / 7 2 2006 2008 9 LVFX PK PD 2009 7 100 mg 1 3 500 mg 1 1 AUC/MIC
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3M TM Chlorhexidine Gluconate IV Securement Dressings Tegaderm TM CHG Support CRBSI Prevention TegadermTM CHG Dressing 2w/w% 60% N. Safdar, Intensive Care Med 2004 30 62-7 Guideline Centers for Disease
VOL.30 NO.10 CHEMOTHERAPY 1123 Fig,1 Group B case 6 hepatolithiasis,e.k.66 y.0.,f.45kg Postoperative wound infection Fig.2 Group B case 15 gastric cancer,k.k.60 y.o.,m. Postoperative peritonitis Fig.3
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Table 1. Concentration of ritipenem in plasma, gallbladder tissue and bile after ritipenem acoxil administration (200 mg t.i.d., 3 days) N.D.: not det
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