Zobrazeno 1 - 10
of 24
pro vyhledávání: '"S F, Kowalsky"'
Publikováno v:
Antimicrobial Agents and Chemotherapy. 40:1153-1156
Many drugs exhibit altered pharmacokinetic parameters in burn patients. We prospectively evaluated the pharmacokinetics of ciprofloxacin in eight burn patients with active infections. Each patient received a 400-mg dose of ciprofloxacin intravenously
Autor:
S F Kowalsky, Abdollah Iravani, D H Sikes, J McCarty, A Heyd, R L Tosiello, E P Whalen, Alan D. Tice, Harry A. Gallis, Thomas Nolen
Publikováno v:
Archives of Internal Medicine. 155:485-494
Background Three studies were undertaken to determine the minimum effective dosing regimen of ciprofloxacin for the treatment of acute, symptomatic, uncomplicated lower urinary tract infection. Methods All studies were multicenter, prospective, rando
Autor:
S F Kowalsky, D M Dixon
Publikováno v:
American Journal of Health-System Pharmacy. 48:827-835
The chemistry, activity, pharmacokinetics, clinical efficacy, adverse effects, drug interactions, and administration of fluconazole are reviewed. Fluconazole is a triazole antifungal agent labeled for use in the treatment of oropharyngeal and esophag
Publikováno v:
The Journal of antimicrobial chemotherapy. 43
The study was undertaken to compare the safety and efficacy of twice-daily ciprofloxacin for 3 days with standard 7 day therapy with either co-trimoxazole or nitrofurantoin in the treatment of women with acute, uncomplicated urinary tract infections
Publikováno v:
The Journal of antimicrobial chemotherapy. 43
To determine the efficacy and safety of single-dose oral ciprofloxacin prophylaxis for the prevention of post-operative bacteriuria following transurethral resection of the prostate or bladder tumour, a prospective, randomized, double-blind, placebo-
Autor:
S F, Kowalsky
Publikováno v:
Pharmacy practice management quarterly. 16(2)
Drug development requires the cooperation and efforts of industry and investigators. If the process is to be successful (i.e., FDA approval), then both industry and investigators must be committed and clearly understand the goals and objectives of th
Autor:
A, Iravani, A D, Tice, J, McCarty, D H, Sikes, T, Nolen, H A, Gallis, E P, Whalen, R L, Tosiello, A, Heyd, S F, Kowalsky
Publikováno v:
Archives of internal medicine. 155(5)
Three studies were undertaken to determine the minimum effective dosing regimen of ciprofloxacin for the treatment of acute, symptomatic, uncomplicated lower urinary tract infection.All studies were multicenter, prospective, randomized, double-blind
Publikováno v:
Clinical nephrology. 39(1)
The pharmacokinetics of a single, oral dose of 750 mg of ciprofloxacin were studied in 35 subjects with various degrees of renal function (Group 1, Clcror = 80 ml/min; Group II, Clcr 50-79 ml/min; Group III, Clcr 10-49 ml/min) and on hemodialysis (HD
Publikováno v:
Clinical pharmacy. 11(5)
Publikováno v:
Hospital formulary. 26(9)
In this 30-hospital survey, data on usage, adverse drug reaction (ADR) rates, and drug interactions (DI) of the H2-receptor antagonists (H2RA) cimetidine, ranitidine, and famotidine were analyzed. Approximately 8% (1,768 patients) admitted to partici