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Pharmacokinetics of ciprofloxacin after oral and parenteral administration.

In 12 fasting volunteers, the pharmacokinetics of ciprofloxacin (Bay o 9867; 1-cyclopropyl-6-fluor-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline carbonic acid) were determined after the administration of 50, 100, and 750 mg orally as well as 50 and 100 mg intravenously over 15 min. Serum and urine...

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Bibliografski detalji
Izdano u:Antimicrob Agents Chemother
Glavni autori: Höffken, G, Lode, H, Prinzing, C, Borner, K, Koeppe, P
Format: Artigo
Jezik:Inglês
Izdano: American Society for Microbiology (ASM) 1985
Teme:
Online pristup:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC176280/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3158275/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/aac.27.3.375
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