Nevirapine is a nonnucleoside reverse transcriptase inhibitor (NNRTI) that
has the most common treatment limiting side effect of rash. Severe rash has
been observed in 3% of patients taking nevirapine in clinical trials, 85%
of whom were men. In a multicenter, retrospective cohort study of all patie
nts who received nevirapine over a 5-year period, severe rash was noted in
9 of 95 women and 3 of 263 men (risk ratio [RR], 8.31; 95% confidence inter
val [CI], 2.3-30.0; P=.005). Women were more likely to discontinue nevirapi
ne therapy because of rash (RR, 4.5; 95% CI, 1.9-10.5; P=.0005). After adju
sting for age and baseline CD4 cell count in multivariate analysis, women h
ad a 7-fold increase in risk for severe rash and were 3.5 times more likely
to discontinue nevirapine therapy. In women of reproductive age for whom c
ontraception may occur, nevirapine remains the NNRTI of choice. Recognition
of sex differences in this severe adverse event will be important in presc
ribing nevirapine.