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Volumn 63, Issue 1, 2007, Pages 121-124
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Comparative bioequivalence study between a novel matrix transdermal delivery system of fentanyl and a commercially available reservoir formulation
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Author keywords
Fentanyl; Matrix transdermal delivery system; Performance; Pharmacokinetics; Safety
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Indexed keywords
FENTANYL;
NALTREXONE;
ADHESION;
ADULT;
APPLICATION SITE REACTION;
AREA UNDER THE CURVE;
ARTICLE;
ATTENTION DISTURBANCE;
BIOEQUIVALENCE;
CLINICAL TRIAL;
COMPARATIVE STUDY;
CONTROLLED CLINICAL TRIAL;
CONTROLLED STUDY;
CROSSOVER PROCEDURE;
DISEASE SEVERITY;
DIZZINESS;
DRUG BLOOD LEVEL;
DRUG DELIVERY SYSTEM;
DRUG EFFICACY;
DRUG FORMULATION;
DRUG SAFETY;
HUMAN;
HUMAN EXPERIMENT;
LIQUID CHROMATOGRAPHY;
MALE;
MASS SPECTROMETRY;
NAUSEA;
NORMAL HUMAN;
PAIN;
PRIORITY JOURNAL;
RANDOMIZED CONTROLLED TRIAL;
SKIN IRRITATION;
SOMNOLENCE;
UNSPECIFIED SIDE EFFECT;
ADMINISTRATION, CUTANEOUS;
ADULT;
ANALGESICS, OPIOID;
CROSS-OVER STUDIES;
DRUG DELIVERY SYSTEMS;
FENTANYL;
HUMANS;
MALE;
MIDDLE AGED;
THERAPEUTIC EQUIVALENCY;
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EID: 33845412248
PISSN: 03065251
EISSN: 13652125
Source Type: Journal
DOI: 10.1111/j.1365-2125.2006.02758.x Document Type: Article |
Times cited : (29)
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References (10)
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