Excretion of Cephaloridine and Cephalothin in Patients with Renal Impairment
- 24 March 1966
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 274 (12) , 654-656
- https://doi.org/10.1056/nejm196603242741205
Abstract
THE cephalosporins are a group of antibiotics isolated from Cephalosporium acremonium in 1945.1 Cephalothin, a semisynthetic derivation of one of these, cephalosporin C, came into general clinical use in 1964. This compound has gained widespread acceptance because of its penicillin-like activity against a wide variety of bacteria, general resistance to staphylococcal penicillinase, low serum protein binding, minimum crossallergenic relation to the penicillins and limited side reactions and toxicity.2 3 4 5 It is poorly absorbed by the oral route and requires parenteral injection. Cephalothin is rapidly excreted into the urine. The major metabolite is a relatively inactive desacetyl analogue.6 Substitution of a pyridine . . .This publication has 11 references indexed in Scilit:
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