PREVIOUS reports on the administration of tetraethylthiuramdisulfide (antabuse®) have listed various symptoms which commonly occur in patients who are taking the drug.1 These symptoms have been found to be fatigue, headache, dizziness, gastrointestinal disturbances, skin allergies, unpleasant taste in the mouth and reduced sexual potency.
Psychosis also has been reported as a complication of tetraethylthiuramdisulfide therapy. Lemieux2 mentioned two patients in whom manic-like reactions developed. One patient's disturbance cleared after withdrawal of the drug; the other's, after reduction of the dose. Bennett, McKeever, and Turk,3 in reporting six cases of psychosis complicating tetraethylthiuramdisulfide therapy, noted a predominant paranoid reaction in two and an expansive trend in one; discontinuance of the drug was necessary with five of the patients; but of these, all had evidence of hepatic damage, and four, symptoms of organic damage to the brain, prior to treatment with tetraethylthiuramdisulfide. Knutsen4 reported the case of
USDIN GL, ROBINSON KE. PSYCHOSIS OCCURRING DURING ANTABUSE ADMINISTRATION. AMA Arch NeurPsych. 1951;66(1):38–43. doi:10.1001/archneurpsyc.1951.02320070058004
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