This case supports the previous reports describing the association between the use of topiramate and the developmenrt of hallucinations. Although the average daily topiramate dose associated with the development of hallucinations in previously reported cases was 150 mg in women and 181 mg in men, hallucinations can occur at lower doses (as low as 50 mg daily) as well.
The selective α1-adrenergic antagonist prazosin has been shown in multiple studies to be effective in targeting trauma-related nightmares in posttraumatic stress disorder. There are limited data regarding the effectiveness of another selective α1-adrenergic antagonist terazosin for the treatment of trauma-related nightmares. We present 4 cases in which terazosin was effectively used to treat nightmares as a second-line agent after prazosin failure. Further studies are needed to validate terazosin as an alternative to prazosin for the treatment of posttraumatic stress disorder-related nightmares.
Background:
Lamotrigine is a phenyltriazine medication that has been approved by the
United States Food and Drug Administration as monotherapy and as an adjunctive agent for the
treatment of seizure disorder. It was later approved by the FDA for the treatment of bipolar disorder.
Lamotrigine is generally well tolerated by patients, but some serious symptoms can occur during
treatment. These severe side effects include rashes and multi-organ failure. Lamotrigine has also
been associated with the development of mental status changes, frequently when used concurrently
with other medications that may impact the metabolism of lamotrigine.
Objective:
To present the case of a 65-year-old man being treated with lamotrigine and valproic acid
who developed mental status changes after the addition of sertraline to his medication regimen,
and to compare this case to existing cases reported in the literature.
Discussion:
Our case adds to the existing literature by demonstrating that patients may experience
adverse medication effects despite lamotrigine levels that are normally considered to be in the therapeutic
range, highlighting the importance of clinical correlation when obtaining medication levels.
Conclusion:
Clinicians should use caution interpreting lamotrigine levels when working up delirium,
as normal levels may not rule out the development of lamotrigine toxicity.
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