Acute transaminitis after initial days of starting haloperidol

Rami Gabriel (School of Medicine, and)
Todd Wojtanowicz (Department of Psychiatry, University of California, Irvine, CA, USA)
Reza Farokhpay (School of Medicine, and) (Department of Psychiatry, University of California, Irvine, CA, USA)
Robert Bota (School of Medicine, and) (Department of Psychiatry, University of California, Irvine, CA, USA)

Mental Illness

ISSN: 2036-7465

Article publication date: 22 March 2019

297
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Abstract

Haloperidol is a first-generation antipsychotic butyrophenone that is lipophilic, readily absorbed, and extensively metabolized in the liver. The occurrence of elevated liver enzymes with haloperidol is reported to be 2.4% with cases generally occurring in the setting of chronic use. In this case, we present a patient who developed elevated liver enzymes 1-2 days after starting haloperidol treatment on two separate occasions and in the context of negative hepatic viral and autoimmune serology. Liver enzymes consistently had alanine transaminase > aspartate transaminase and peaked at 288 U/L prior to discontinuation of the medication. The patient was taken off haloperidol after serology resulted and clozapine regimen started. He was able to tolerate clozapine well with recovery of his transaminitis and psychiatric stabilization.

Keywords

Citation

Gabriel, R., Wojtanowicz, T., Farokhpay, R. and Bota, R. (2019), "Acute transaminitis after initial days of starting haloperidol", Mental Illness, Vol. 11 No. 1, pp. 33-35. https://doi.org/10.1108/mi.2019.8113

Publisher

:

Emerald Publishing Limited

Copyright © 2019 R. Gabriel et al.

License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).


Corresponding author

Robert Bota, University of California, Irvine, UCIMC, Bldg 3, Rt 88, Orange, CA 92868, USA. Tel.: +1.714.4562056.

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