Determination of bioequivalence of two furosemide preparations; The effect of high doses of furosemide on some pharmacokinetic parameters

International Journal of Clinical Pharmacology Research

Volumn 16, Issue 4-5, 1996, Pages 83-88

  Wolf Coporda A ^a   Lovric Z ^a   Huic, M ^b   Francetic I ^b   Vrhovac, B ^b   Plavsic F ^a   Skreblin M ^c  

^a UNIVERSITY OF ZAGREB   (Croatia)

^b KBC Zagreb   (Croatia)

^c Analytical Development Department   (Croatia)

Author keywords

[No Author keywords available]

Indexed keywords

FUROSEMIDE;

ADULT; AREA UNDER THE CURVE; ARTICLE; BIOEQUIVALENCE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CROATIA; CROSSOVER PROCEDURE; DRUG ABSORPTION; DRUG BIOAVAILABILITY; DRUG BLOOD LEVEL; DRUG FORMULATION; DRUG HALF LIFE; DRUG RELEASE; FLUORESCENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN EXPERIMENT; LABORATORY TEST; MALE; NORMAL HUMAN; ORAL DRUG ADMINISTRATION; QUALITY CONTROL; RANDOMIZED CONTROLLED TRIAL; STATISTICAL ANALYSIS; TIME;

ADULT; ANALYSIS OF VARIANCE; BIOLOGICAL AVAILABILITY; CROSS-OVER STUDIES; DIURETICS; FUROSEMIDE; HALF-LIFE; HUMANS; MALE; THERAPEUTIC EQUIVALENCY;

EID: 0030440122     PISSN: 02511649     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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