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Volumn 73, Issue 8, 2014, Pages 1549-1551
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Head-to-head, randomised, crossover study of oral versus subcutaneous methotrexate in patients with rheumatoid arthritis: Drug-exposure limitations of oral methotrexate at doses ≥15 mg may be overcome with subcutaneous administration
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Author keywords
[No Author keywords available]
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Indexed keywords
METHOTREXATE;
ADULT;
AREA UNDER THE CURVE;
ARTICLE;
AUTOINJECTOR;
BIOEQUIVALENCE;
CLINICAL ARTICLE;
CONTROLLED STUDY;
CROSSOVER PROCEDURE;
DRUG BIOAVAILABILITY;
DRUG BLOOD LEVEL;
DRUG DOSAGE FORM COMPARISON;
DRUG EXPOSURE;
DRUG FATALITY;
DRUG HALF LIFE;
DRUG SAFETY;
DRUG SUBSTITUTION;
DRUG TOLERABILITY;
FEMALE;
HUMAN;
INJECTION SITE;
MALE;
MAXIMUM PLASMA CONCENTRATION;
MULTICENTER STUDY;
OPEN STUDY;
PHASE 2 CLINICAL TRIAL;
PRIORITY JOURNAL;
RANDOMIZED CONTROLLED TRIAL;
RHEUMATOID ARTHRITIS;
THIGH;
TIME TO MAXIMUM PLASMA CONCENTRATION;
TREATMENT RESPONSE;
UNSPECIFIED SIDE EFFECT;
METHOTREXATE;
PHARMACOKINETICS;
RHEUMATOID ARTHRITIS;
ADMINISTRATION, ORAL;
AGED;
ANTIRHEUMATIC AGENTS;
ARTHRITIS, RHEUMATOID;
CROSS-OVER STUDIES;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG ADMINISTRATION ROUTES;
FEMALE;
HUMANS;
INJECTIONS, SUBCUTANEOUS;
MALE;
METHOTREXATE;
MIDDLE AGED;
SELF ADMINISTRATION;
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EID: 84903893560
PISSN: 00034967
EISSN: 14682060
Source Type: Journal
DOI: 10.1136/annrheumdis-2014-205228 Document Type: Article |
Times cited : (152)
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References (9)
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