The recently recognized high morbidity and unexpected mortality associ
ated with rheumatoid arthritis (RA) has spurred new interest in more a
ggressive, early treatment of this disease. Methotrexate (MTX) has rap
idly become the rheumatologist's drug of choice for serious RA because
of its favorable efficacy to toxicity ratio and rapid onset of action
compared with other second-line agents. The initial concerns about he
patic fibrosis and cirrhosis in psoriatic patients has subsided somewh
at as long-term liver toxicity data are accumulating in patients with
RA. Routine liver biopsy with incremental doses of MTX is no longer re
commended. Potential for severe lung, hematologic, and infectious comp
lications exists, mandating careful monitoring of RA patients taking M
TX.