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A multicenter study of the safety and efficacy of naproxen: analysis of blood pressure.

Abstract
A multicenter study was conducted to determine safety and efficacy of naproxen, 500 mg twice daily, administered for 4 weeks to osteoarthritis (OA) patients. OA symptoms improved in the study population. The study population included 97 patients, 43 of whom were 65 years of age or older. Forty-four of the 97 patients had a history of hypertension; 42 of these took antihypertensive medication before and during the study. Baseline blood pressure (BP) was measured in most patients while they were receiving their prior nonsteroidal antiinflammatory drug (NSAID) therapy; from that baseline, no increase in BP was seen in the hypertensive or normotensive patients after 4 weeks of naproxen therapy. In patients whose BP was controlled by antihypertensive agents, BP remained under control during naproxen therapy.
AuthorsM A Goldberg
JournalSeminars in arthritis and rheumatism (Semin Arthritis Rheum) Vol. 17 Issue 3 Suppl 2 Pg. 23-8 (Feb 1988) ISSN: 0049-0172 [Print] United States
PMID3334107 (Publication Type: Clinical Trial, Journal Article, Multicenter Study)
Chemical References
  • Naproxen
Topics
  • Adult
  • Aged
  • Blood Pressure (drug effects)
  • Humans
  • Hypertension (complications)
  • Middle Aged
  • Multicenter Studies as Topic
  • Naproxen (administration & dosage, adverse effects, therapeutic use)
  • Osteoarthritis (drug therapy)
  • Safety

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