The toxicity of isoniazid chemoprophylaxis was assessed in 83 health care w
orkers (HCWs) receiving a 6-month course, in whom clinical toxicity and liv
er function were monitored. Thirty-four HCWs (41%) developed an adverse eve
nt; in 26 (76%), toxicity was sufficiently severe to require cessation of t
reatment. Of the total, liver function test abnormalities (serum alanine tr
ansaminase levels more than two times normal) were evident in 14 subjects,
with 8 requiring cessation of therapy. Other symptoms reported included mal
aise, nausea with associated anorexia, arthralgia, and rash. Mean time to d
evelopment of symptoms was 3 weeks (range, 0.5-6 weeks), with the mean age
of those with toxicity not differing significantly from those without (38 v
s. 39 years). The high rate of toxicity seen in this study is sufficiently
notable that we advocate the use of monthly liver function testing and freq
uent review in those receiving isoniazid prophylactic therapy.