In an overview of controlled trials, it is shown that bactericidal dru
gs increase the short-term risk of Type I reactions, but prevent the l
ong-term development of new impairments caused by bacterial proliferat
ion. Clinical experience suggests that the clofazimine component of mu
ltiple drug therapy (MDT) has reduced the incidence of Type II reactio
ns or erythema nodosum leprosum (ENL). The principal impact of MDT, co
mpared with monotherapy, has been to reduce the duration of active dis
ease, thus preventing the deterioration of disability scores. Reductio
n of population disability rates is mainly achieved by earlier detecti
on and treatment. MDT has a number of indirect benefits such as improv
ed compliance, decreased cost, and increased motivation and availabili
ty of leprosy workers. However, MDT must be supplemented by other meas
ures to prevent and treat disabilities.