Pharmacokinetics of single intravenous and intramuscular doses of cefotetan in normal human volunteers
- 1 January 1983
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Antimicrobial Chemotherapy
- Vol. 11 (suppl A) , 201-206
- https://doi.org/10.1093/jac/11.suppl_a.201
Abstract
The pharmacokinetic parameters of cefotetan were determined in six healthy adults after intramuscular (im) and intravenous (iv) administration of a single dose. After an iv bolus injection of 1 g cefotetan the mean peak serum level was 179.6 mg/l ( s.e.m. ± 14.2 mg/l) at 2 min. The apparent volume of distribution was 10.29 1 ( s.e.m. ±0.661). After im injections of 500 mg and 1 g of cefotetan the mean peak levels were 35 mg/l ( s.e.m. ±1.6 mg/l) and 74 mg/l ( s.e.m. ±3.6 mg/l) at 82 and 97 min respectively; the level at 12 h was 4.5 mg/l after 500 mg and 10.4 mg/l after 1 g. Cefotetan was slowly eliminated. The serum half-life was about 3.1 h after 1 g iv injection and varied from 3.4 to 3.7 h after the 500 mg and 1 g im injections. About 75 % of the dose was excreted in the urine during the first 24 h after 1 g iv bolus injection; after 500 mg and 1 g im injection 60 to 65% of the dose was recovered in the urine during the sarde time period.Keywords
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