Because thiacetazone has been linked with serious adverse cutaneous re
actions, we undertook 1 year of systematic surveillance for cutaneous
thiacetazone-associated adverse reactions within the national tubercul
osis programme of Tanzania, For individual cases, we collected informa
tion on age, sex, interval between commencing thiacetazone-containing
treatment and occurrence of adverse reaction, most severe clinical pre
sentation (toxic epidermal necrolysis, rash without necrolysis, itchin
g without rash), and outcome (dead or alive) within 2 weeks of onset,
Univariate and multivariate analyses were done of variables relevant t
o outcome. 1273 patients with adverse reactions were reported, The fre
quency of fatal outcome from any cutaneous reaction was 3.1 per 1000 a
mong all tuberculosis patients, and 19.1% among patients with toxic ep
idermal necrolysis. About 60% of all adverse reactions and deaths occu
rred within 20 days of starling thiacetazone. Case fatality from adver
se cutaneous reactions was considerably less frequent than reported pr
eviously, suggesting that improved management might allow retention of
thiacetazone in the armamentarium of national tuberculosis programmes
even where infection with HIV is prevalent,