In vitro activity of piperacillin, ticarcillin, mezlocillin, ticarcillin-clavulanic acid, aztreonam, ceftazidime, azlocillin, cefoperazone, and thienamycin against Pseudomonas aeruginosa

Clin Ther. 1986;8(6):655-7.

Abstract

The in vitro susceptibility of 103 well-characterized strains of Pseudomonas aeruginosa to nine antimicrobial agents was assessed by means of the Kirby-Bauer disk diffusion assay and the microtiter minimal inhibitory concentration assay. The antimicrobials, from the most to the least active against P aeruginosa, were thienamycin greater than ceftazidime greater than piperacillin greater than azlocillin greater than cefoperazone greater than aztreonam greater than ticarcillin greater than ticarcillin-clavulanic acid greater than mezlocillin. The resistance patterns of the antimicrobial agents suggest that P aeruginosa resistant to a penicillin, cephalosporin, or aztreonam may be susceptible to thienamycin.

MeSH terms

  • Anti-Bacterial Agents / pharmacology*
  • Azlocillin / pharmacology
  • Aztreonam / pharmacology
  • Cefoperazone / pharmacology
  • Ceftazidime / pharmacology
  • Clavulanic Acid
  • Clavulanic Acids / pharmacology
  • Drug Combinations
  • Mezlocillin / pharmacology
  • Microbial Sensitivity Tests
  • Piperacillin / pharmacology
  • Pseudomonas aeruginosa / drug effects*
  • Thienamycins / pharmacology
  • Ticarcillin / pharmacology

Substances

  • Anti-Bacterial Agents
  • Clavulanic Acids
  • Drug Combinations
  • Thienamycins
  • Clavulanic Acid
  • Cefoperazone
  • Ceftazidime
  • Ticarcillin
  • Aztreonam
  • Azlocillin
  • Mezlocillin
  • thienamycin
  • Piperacillin