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Publikováno v:
British Journal of Clinical Pharmacology. 46:363-367
Aims The aim of this study was to determine the potential impact of age on the pharmacokinetics of temocapril and its pharmacologically active diacid metabolite, temocaprilat, in hypertensive patients. Methods Male and female patients with mild to mo
Publikováno v:
British journal of clinical pharmacology. 46(4)
The aim of this study was to determine the potential impact of age on the pharmacokinetics of temocapril and its pharmacologically active diacid metabolite, temocaprilat, in hypertensive patients.Male and female patients with mild to moderate essenti
Autor:
A. T. J. Lavrijssen, Hans-Hellmut Neumayer, K. Püchler, B. Sierakowski, Lutz Fritsche, T. Thomsen, K. M. Eckl, Ivar Roots, K. Renneisen
Publikováno v:
British journal of clinical pharmacology. 44(6)
AIMS The aim of this study was to determine the potential influence of renal impairment on the pharmacokinetics of temocapril and its pharmacologically active diacid metabolite, temocaprilat. METHODS Non-compartmental pharmacokinetics were assessed i
Publikováno v:
European journal of clinical pharmacology. 53(3-4)
The aim of this study was to determine the influence of renal impairment on the single-dose pharmacokinetics of temocapril and its pharmacologically active metabolite, temocapril diacid.A single oral dose of 20 mg temocapril hydrochloride was given a
Publikováno v:
Medizinische Klinik (Munich, Germany : 1983). 89(8)
Spirapril is a recent ACE inhibitor with a both renal and hepatic elimination pathway. In order to determine its tolerability, primarily the impact on renal function, Spirapril was tested in a single-blind trial with a 2-week placebo run-in phase and
Publikováno v:
Blood pressure. Supplement. 2
In this single-blind trial with a 2-week placebo run-in followed by a 4-week active-treatment period, patients were given 6 mg of spirapril once daily. Forty-nine hypertensive men and women were recruited; all had pretreatment diastolic blood pressur
Publikováno v:
Blood pressure. Supplement. 2
A total of 171 male and female patients with mild-to-moderate hypertension [diastolic blood pressure (DBP) 100-115 mmHg] entered this randomized, double-blind, multicentre study. A 3-week placebo run-in period was followed by a 5-week active-treatmen
Publikováno v:
Blood pressure. Supplement. 2
In a single-blind trial with a 2-week placebo run-in phase and a 4-week active-treatment period, spirapril at 6 mg once daily was administered to 49 consecutive hypertensive patients (34 men and 15 women). All had pretreatment diastolic blood pressur
Publikováno v:
Blood pressure. Supplement. 2