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PMID: 3555028 Published · ppublish English Clinical Trial Controlled Clinical Trial Journal Article

Pharmacokinetics of two dosage regimens of ciprofloxacin during a two-week therapeutic trial in patients with cystic fibrosis.

The American journal of medicine ·Vol. 82 ·No. 4A ·1987-04-27 ·Pages 142-5

Stutman HR, Shalit I, Marks MI, Greenwood R, Chartrand SA, Hilman BC

Abstract

Twenty-nine adult patients with cystic fibrosis received 750 or 1,000 mg of ciprofloxacin orally every 12 hours for two weeks. Pharmacokinetic data were collected on Days 1, 7, and 14. Pharmacokinetic analyses revealed minor differences between the dosage regimens, and results were similar on the first, seventh, and last day of therapy. Means for peak serum concentration (3.1 to 5.0 micrograms/ml), elimination half-life (4.8 to 5.3 hours), area under the time-concentration curve, and serum clearance (36.8 to 44.5 liter/hour) were similar to previously reported results for patients without cystic fibrosis. Sputum concentrations approximated serum values.

MeSH Terms
Adult Ciprofloxacin/administration & dosage,metabolism,therapeutic use Clinical Trials as Topic Cystic Fibrosis/complications,drug therapy,metabolism Female Humans Kinetics Male Respiratory Tract Infections/complications,drug therapy,metabolism Sputum/metabolism
Chemicals
Ciprofloxacin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Stutman H R
Shalit I
Marks M I
Greenwood R
Chartrand S A
Hilman B C
Article Info
Journal
The American journal of medicine
Abbr.
Am J Med
ISSN
0002-9343
Published
1987-04-27
Pages
142-5
Language
English
Region
United States
NLM ID
0267200
Subset
IM
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