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Volumn 5, Issue 8, 2001, Pages 691-695
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The potential use of urinary excretion data for assessing the relative bioavailability of rifampicin in fixed dose combination anti-tuberculosis formulations
a a a a |
Author keywords
Fixed dose combination; Relative bioavailability; Rifampicin; Tuberculosis; Urinary excretion
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Indexed keywords
DEACETYLRIFAMPICIN;
ETHAMBUTOL;
ISONIAZID;
PYRAZINAMIDE;
RIFAMPICIN;
RIFAMPICIN DERIVATIVE;
TUBERCULOSTATIC AGENT;
UNCLASSIFIED DRUG;
AREA UNDER THE CURVE;
ARTICLE;
BIOEQUIVALENCE;
CLINICAL TRIAL;
COLORIMETRY;
COMBINATION CHEMOTHERAPY;
CONCENTRATION RESPONSE;
CONTROLLED CLINICAL TRIAL;
CONTROLLED STUDY;
CROSSOVER PROCEDURE;
DIAGNOSTIC VALUE;
DOSE RESPONSE;
DOSE TIME EFFECT RELATION;
DRUG BIOAVAILABILITY;
DRUG BLOOD LEVEL;
DRUG FORMULATION;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HUMAN;
HUMAN EXPERIMENT;
MALE;
NON INVASIVE MEASUREMENT;
NORMAL HUMAN;
PRIORITY JOURNAL;
RANDOMIZED CONTROLLED TRIAL;
TUBERCULOSIS;
URINARY EXCRETION;
ANTIBIOTICS, ANTITUBERCULAR;
AREA UNDER CURVE;
BIOLOGICAL AVAILABILITY;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
COLORIMETRY;
CROSS-OVER STUDIES;
DRUG COMBINATIONS;
ETHAMBUTOL;
HUMANS;
ISONIAZID;
MALE;
PYRAZINAMIDE;
QUALITY CONTROL;
REFERENCE VALUES;
RIFAMPIN;
THERAPEUTIC EQUIVALENCY;
TUBERCULOSIS;
URINALYSIS;
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EID: 0034906127
PISSN: 10273719
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (10)
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References (19)
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