There are few reports in the literature related to sulfonylurea-induced hep
atotoxicity. We describe the case of acute hepatitis induced by gliclazide,
a second generation sulfonylurea. A 60-year-old woman with diabetes mellit
us (type 2) developed an acute icteric hepatitis-like illness 6 weeks after
the initiation of gliclazide therapy. Other causes of acute hepatocellular
necrosis were excluded. Liver histology showed marked portal inflammation
with lymphocytes, monocytes and eosinophils, associated with lobular inflam
mation (indicative of a histological pattern consistent with drug-induced h
epatitis). The drug was immediately withdrawn and the patient was given gli
benclamide. The patient recovered clinically and, in less than 4 weeks, her
serum bilirubin and aminotransferases returned to normal levels. We believ
e that this is the first description of acute hepatitis caused by an idiosy
ncratic adverse reaction to gliclazide or to one of its metabolites. In con
clusion, this case strongly suggests that gliclazide can induce acute icter
ic liver necro-inflammation which may be misdiagnosed clinically as acute v
iral hepatitis. In patients who show abnormal liver function tests, the imm
ediate discontinuation of gliclazide is recommended. (C) 2000 Lippincott Wi
lliams & Wilkins.