Pharmacokinetic Interpretation of Cephradine Levels in Serum After Intravenous and Extravascular Administration in Humans

Author:

Rattie Elisabeth S.1,Bernardo Peter D.1,Ravin Louis J.1

Affiliation:

1. Research and Development Division, Smith Kline and French Laboratories, Philadelphia, Pennsylvania 19101

Abstract

Pharmacokinetic parameters were calculated from intravenous data based upon a two-compartment open model. These parameters were subsequently used to determine the absorption rates and bioavailability of cephradine administered intramuscularly and orally. The results indicate that cephradine obeys dose-independent kinetics and that biological availability is complete from all dosage forms.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference10 articles.

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2. Grove D. C. and W. A. Randall. 1955. Assay methods of antibiotics: a laboratory manual. Medical Encyclopedia Inc. New York.

3. Cephradine absorption and excretion in fasting and non-fasting volunteers;Harvengt C.;J. Clin. Pharmacol.,1973

4. Cephradine: antibacterial activity and clinical effectiveness;Klastersky J.;Chemotherapy,1973

5. Cephradine in the treatment of intestinal infections caused by Shigella or Salmonella organisms;Landa L.;Curr. Ther. Res. Clin. Exp.,1972

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