Effect of Probenecid on the Blood Levels and Urinary Excretion of Cefamandole

Author:

Griffith R. S.1,Black H. R.2,Brier G. L.2,Wolny J. D.2

Affiliation:

1. Lilly Laboratory for Clinical Research, Wishard Memorial Hospital, Indianapolis, Indiana 46202

2. Indiana University School of Medicine, Indianapolis, Indiana 46202

Abstract

Two oral 0.5-g doses of probenecid given 7 and 1 h before a single 1-g intramuscular dose of cefamandole resulted in higher serum levels of cefamandole than when cefamandole was given alone: 37 versus 20 μg per ml of serum, respectively. Cefamandole was not measurable (<0.3 μg/ml) at 8 h when it was given alone, whereas an average 8-h value of 2.9 μg/ml was obtained after pretreatment with probenecid. By prolonging the duration of these high cefamandole levels, probenecid should permit the treatment of more serious clinical infections, including those due to relatively resistant organisms, or permit a reduction in either the dosage of cefamandole or the frequency of administration.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference6 articles.

1. Brazeau P. 1975. Inhibitors of tubular transport of organic compounds p. 860-866. In L. S. Goodman and A. Gilman (ed.) The pharmacological basis of therapeutics 5th ed. Macmillan Publishing Co. Inc. New York.

2. Clinical pharmacology of cefamandole as compared with cephalothin;Fong I. W.;Antimicrob. Agents Chemother.,1976

3. Cefamandole: in vitro and clinical pharmacokinetics;Griffith R. S.;Antimicrob. Agents Chemother.,1976

4. Grove D. and W. A. Randall. 1955. Assay methods for antibiotics. Antibiot. Monogr. Vol. 2.

5. Pharmacokinetics of cefazolin compared with four other cephalosporins;Kirby W. M. M.;J. Infect. Dis.,1973

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