In Vitro Susceptibility of Nocardia asteroides to N -Formimidoyl Thienamycin and Several Cephalosporins

Author:

Cynamon Michael H.1,Palmer Gregory S.1

Affiliation:

1. Department of Medicine, Veterans Administration Medical Center and State University of New York, Upstate Medical Center, Syracuse, New York 13210

Abstract

The susceptibility of N. asteroides to N -formimidoyl thienamycin, cefamandole, cefoxitin, and moxalactam was determined by agar dilution. N -Formimidoyl thienamycin was the most active, inhibiting eight of nine strains at 1.56 μg/ml.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference8 articles.

1. Susceptibility of Nocardia asteroidex to 45 antimicrobial agents in vitro;Bach M. C.;Antimicrob. Agents Chemother.,1973

2. A method for determining in vitro drug susceptibilities of some nocardiae and actinomadurae;Carroll G. F.;Am. J. Clin. Pathol.,1977

3. In vitro susceptibility of Nocardia asteroides to amikacin;Dalovisio J. R.;Antiniicrob. Agents Chemother.,1978

4. In vitro activity of cefoxitin against nocardia spp. and actinomadura spp;Garcia-Rodriguez J. A.;J. Antimicrob. Chemother.,1979

5. Lerner P. L. Nocardia species p. 1962-1969. In G. L Mandell R. G. Douglas Jr. and J. E. Bennett (ed.) Principles and practice of infectious diseases. John Wiley & Sons Inc. New York.

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