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Antiepileptic Drug Hypersensitivity Syndrome
Authors:Raymond G. Schlienger,&dagger  Neil H. Shear
Affiliation:Divisions of Clinical Pharmacology, Sunnybrook Health Science Centre, University of Toronto, Toronto, Ontario, Canada;Divisions of Dermatology, Departments of Medicine, Pharmacology, and Pharmacy, and the Glaxo Wellcome-Sunnybrook Drug Safety Clinic, Sunnybrook Health Science Centre, University of Toronto, Toronto, Ontario, Canada
Abstract:Summary: : The antiepileptic drug hypersensitivity syndrome (AHS) is an adverse drug reaction associated with the aromatic antiepileptic drugs (AEDs) phenytoin (PHT), carbamazepine (CBZ), phenobarbital (PB), and primidone. The syndrome is defined by the triad of fever, skin rash, and internal organ involvement. It can also be caused by other drugs, such as sulfonamides, dapsone, minocycline, terbinafine, azathioprine, and allopurinol. Diagnosis of AHS may be difficult because of the variety of clinical and laboratory abnormalities and manifestations and because the syndrome may mimic infectious, neoplastic, or collagen vascular disorders. The incidence is approximately 1 in 3,000 exposures. AHS starts with fever, rash, and lymphadenopathy, within the fist 2–8 weeks after initiation of therapy. Internal manifestations include, among others, agranulocytosis, hepatitis, nephritis, and myostitis. AHS is associated with a relative excess of reactive oxidative metabolites of the AED. Insufficient detoxification may lead to cell death or contribute to the formation of antigen that triggers an immune reaction. Crossreactivity among PHT, CBZ, and PB is as high as 70–80%.
Keywords:Antiepileptic drugs    Adverse drug reaction    Hypersensitivity    Syndrome
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