Abstract |
The development of oxaprozin provided an opportunity to evaluate the control of inflammation in rheumatoid arthritis by a drug that can be administered once daily. A double-blind 12-week evaluation suggested comparable efficacy between 1,200 mg oxaprozin given as a single daily dose and 3,900 mg ASA given in 4 equally divided doses. A lower incidence of side effects was noted in the oxaprozin group. An open 6-month study substantiated the efficacy and safety of oxaprozin.
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Authors | W J Reynolds, S F Shaar, A Buik, W J Lancee |
Journal | The Journal of rheumatology
(J Rheumatol)
1979 May-Jun
Vol. 6
Issue 3
Pg. 345-50
ISSN: 0315-162X [Print] Canada |
PMID | 385873
(Publication Type: Clinical Trial, Comparative Study, Controlled Clinical Trial, Journal Article)
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Chemical References |
- Oxazoles
- Propionates
- Aspirin
|
Topics |
- Arthritis, Rheumatoid
(drug therapy)
- Aspirin
(administration & dosage, therapeutic use)
- Chemical Phenomena
- Chemistry
- Clinical Trials as Topic
- Double-Blind Method
- Drug Evaluation
- Humans
- Oxazoles
(administration & dosage, therapeutic use)
- Propionates
(administration & dosage, therapeutic use)
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