Volume 9, Issue 3 pp. 310-313

Two case reports of oral ulcers with lamotrigine several weeks after oxcarbazepine withdrawal

Amy O'Neill

Amy O'Neill

University of Kentucky, Mental Health Research Center at Eastern State Hospital and the Department of Psychiatry, University of Kentucky, Lexington, KY, USA

Search for more papers by this author
Jose De Leon

Jose De Leon

University of Kentucky, Mental Health Research Center at Eastern State Hospital and the Department of Psychiatry, University of Kentucky, Lexington, KY, USA

Search for more papers by this author
First published: 05 April 2007
Citations: 13
Jose de Leon, MD, Mental Health Research Center at Eastern State Hospital, 627 West Fourth Street, Lexington, KY 40508, USA.
Fax: +1 859 246 7019;
e-mail: [email protected]

These patients were studied with no external support. In the past 2 years, JdL has received researcher-initiated grants from Eli Lilly & Co. and Roche Molecular Systems, Inc.; has served on the advisory board of Bristol-Myers Squibb; and has presented 2 lectures with support from Eli Lilly & Co. and Roche Molecular Systems, Inc., respectively. AON has no reported conflicts of interest.

Abstract

Objective: To report two cases of mouth ulcers in lamotrigine patients after oxcarbazepine withdrawal.

Patients and methods: The first patient was a 35-year-old woman with bipolar disorder II (BD II) started on lamotrigine and tapered off oxcarbazepine while an inpatient. The second patient was a 36-year-old man with BD II. He was discharged on lamotrigine and oxcarbazepine with the recommendation of a slow withdrawal of oxcarbazepine.

Results: Many weeks after hospital discharge and after a stable lamotrigine dose had been established, both patients developed painful mouth ulcers that were diagnosed during outpatient visits. The first patient developed ulcers 39 days after oxcarbazepine was stopped and the ulcers resolved 4 days after lamotrigine discontinuation. The second patient was taking 1200 mg/day of oxcarbazepine and after leaving hospital decreased this to 600 mg/day. Twenty-two days after the oxcarbazepine decrease, he developed oral ulcers that resolved with oxcarbazepine and lamotrigine discontinuation.

Conclusions: Lamotrigine is mainly metabolized by glucuronidation, specifically by the uridine 5′-diphosphate glucuronosyltransferases 1A4 (UGT1A4). Carbamazepine is a UGT1A4 inducer. These two cases suggest that oxcarbazepine may also induce lamotrigine metabolism. The discontinuation or dosage decrease of carbamazepine or oxcarbazepine may be associated with a slow increase of lamotrigine levels over several weeks and thus increase risk of lamotrigine toxicity that may manifest as oral ulcers. Hospital psychiatrists need to be aware that discontinuation of inducers may take several weeks to manifest as side effects.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.