The pharmacokinetics of cefuroxime after intravenous injection
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Pharmacology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF00609865.pdf
Reference17 articles.
1. O'Callaghan, Cynthia H., Sykes, R.B., Ryan, D.M., Foord, R.D., Muggleton, P.W.: Cefuroxime ? a new cephalosporin antibiotic. J. Antibiot. (Tokyo),29, 29?37 (1976)
2. O'Callaghan, Cynthia H., Sykes, R.B., Griffiths, A., Thornton, J.E.: Cefuroxime, a new cephalosporin antibiotic: activity in vitro. Antimicrob. Agents Chemother.9, 511?519 (1976)
3. Goodwin, C.S., Dash, C.H., Hill, Joyce, P., Goldberg, A.D.: Cefuroxime: pharmacokinetics after a short infusion, and in vitro activity against hospital pathogens. J. Antimicrob. Chemother.3, 253?261 (1977)
4. Foord, R.D.: Cefuroxime: human pharmacokinetics. Antimicrob. Agents Chemother.9, 741?747 (1976)
5. Goodwin, C.S., Raftery, E.B., Goldberg, A.D., Skeggs, H., Till, A.E., Martin, C.M.: Effects of rate of infusion and probenecid on serum levels, renal excretion, and tolerance of intravenous doses of cefoxitin in humans: comparison with cephalothin. Antimicrob. Agents Chemother.6, 338?346 (1974)
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