1. Academic Validation
  2. Cefamandole: in vitro and clinical pharmacokinetics

Cefamandole: in vitro and clinical pharmacokinetics

  • Antimicrob Agents Chemother. 1976 Nov;10(5):814-23. doi: 10.1128/AAC.10.5.814.
R S Griffith H R Black G L Brier J D Wolny
Abstract

Cefamandole has a broader spectrum and greater potency than the Other cephalosporins. It includes Haemophilus influenzae, most strains of Enterobacter, and many strains of indole-positive Proteus and Bacteroides, with a lower minimal inhibitory concentration for Escherichia coli, Klebsiella, etc. Concentrations of drug in the serum after the parenteral injection of cefamandole exceed manyfold the minimal inhibitory concentrations of over 82% of the bacteria studied. Approximately 65 to 85% is excreted in a biologically active form in the urine. This Antibiotic offers advantages of Antibacterial effectiveness and at the same time retains the safety of penicillin G and cephalothin in Animals.

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