The aim of this study was to determine whether lamotrigine can be re-introd
uced safely and with a benefit in young people who previously had a mild ra
sh associated with the first introduction of this drug. In the first 150 yo
ung people (5-19 years old) treated with lamotrigine in a special centre fo
r epilepsy, seven developed a mild rash soon after starting the drug. In no
ne of these cases was the rash severe, nor was there any mucous membrane in
volvement. The lamotrigine was stopped immediately when the rash was identi
fied and was subsequently re-introduced, using a special very-low-dose-esca
lation regime, starting with 0.1 mg/day total daily dose, after periods ran
ging from 47 to 236 days. It was possible to re-introduce the lamotrigine w
ithout recurrence of persistent rash and without any adverse effects in all
seven cases. The re-introduction of lamotrigine was associated with improv
ement in five of the seven cases. It is recommended that lamotrigine is sto
pped as soon as any rash attributable to the drug develops but it may be po
ssible to re-introduce the drug after mild rash using a very-slow-dose-esca
lation regime, with a benefit in at least some cases. (C) 2000 BEA Trading
Ltd.