R. Bakshi, COMPARATIVE EFFICACY AND TOLERABILITY OF 2 DICLOFENAC FORMULATIONS INTHE TREATMENT OF PAINFUL OSTEOARTHRITIS, British journal of clinical practice, 50(6), 1996, pp. 294-297
The efficacy and tolerability of a new resinate formulation of diclofe
nac 75mg taken once or twice daily were compared with that of conventi
onal enteric-coated diclofenac sodium 50mg tablets given two or three
times daily in a double-blind, randomised, between-patient, 12-week tr
ial in 216 adult patients suffering from painful osteoarthritis of the
hip and/or knee. Similar and clinically significant reductions in the
mean intensity scores of pain at rest or on activity were observed af
ter treatment with either formulation. Global evaluations showed the o
verall response rate to range between 60% and 75%. A significant analg
esic effect was obtained within two weeks of treatment with 150mg dicl
ofenac daily; this improvement was maintained on reduction of the dosa
ge to 75-100mg over the next ten weeks. One or more drug-related adver
se events, predominantly gastrointestinal adverse events, were reporte
d by 40% and 38% of patients in the diclofenac resinate and diclofenac
sodium groups, respectively.