J. Fries, TOWARD AN UNDERSTANDING OF NSAID-RELATED ADVERSE EVENTS - THE CONTRIBUTION OF LONGITUDINAL DATA, Scandinavian journal of rheumatology, 1996, pp. 3-8
The ARAMIS (Arthritis, Rheumatism and Ageing Medical information Syste
m) databanks have been used to objectify and quantify drug toxicity. T
he relative risk of a gastrointestinal (GI)-provoked hospitalization w
as more than five times greater in patients taking non-steroidal anti-
inflammatory drugs.(NSAIDs) than in non-NSAID-treated patients, with a
n excess hospitalization rate of 1.3% per annum. Additionally, there w
as an excess GI-related death rate of around 3% in rheumatoid arthriti
s (RA) patients compared with the normal population. Age, previous NSA
ID-related GI events, prednisone use, higher doses and greater disabil
ity predicted high-risk patients. A toxicity index showed clear differ
ences between NSAIDs, with aspirin, salsalate and ibuprofen emerging a
s the least toxic, and meclofenamate and indomethacin as the most toxi
c. Disease modifying anti-rheumatic drugs (DMARDs) were, surprisingly,
found to have similar toxicity scores to the NSAIDs. This supports th
e contemporary practice of employing DMARDs earlier and more aggressiv
ely in the course of RA.