Anorgasmia in a patient with bipolar disorder type 1 treated with gabapentin

Citation
Ge. Brannon et Pd. Rolland, Anorgasmia in a patient with bipolar disorder type 1 treated with gabapentin, J CL PSYCH, 20(3), 2000, pp. 379-381
Citations number
19
Categorie Soggetti
Pharmacology,"Neurosciences & Behavoir
Journal title
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY
ISSN journal
02710749 → ACNP
Volume
20
Issue
3
Year of publication
2000
Pages
379 - 381
Database
ISI
SICI code
0271-0749(200006)20:3<379:AIAPWB>2.0.ZU;2-4
Abstract
Gabapentin is a relatively new anticonvulsant indicated for adjunctive ther apy in the treatment of partial seizures, with and without secondary genera lization, in adults with epilepsy. Overall, it has a minimal side effect pr ofile compared with other anticonvulsant agents. Postmarketing surveillance is needed to further delineate the spectrum of adverse events that may be experienced by patients treated with this medication. This is a case report of a 25-year-old man with a 10-year history of mood swings that progressiv ely worsened and resulted in a suicide attempt 8 months before his first ap pointment. A diagnosis of bipolar disorder was established, and a clinical interview ruled out other mental disorders. The patient was administered ga bapentin 300 mg/day, and the dose was titrated upward to 900 mg/day, A foll ow-up appointment revealed improved control of his bipolar symptoms. Howeve r, the patient reported that he could not have an orgasm during sexual inte rcourse. The medication was changed to valproic acid 250 mg three times dai ly. His bipolar symptoms remained under control and the anorgasmia resolved , This was maintained at the next follow-up appointment. The side effect pr ofile and therapeutic monitoring requirements of gabapentin are favorable w hen compared with those of other anticonvulsant agents. However, because th is agent is relatively new, especially for use in the treatment of bipolar disorder, a more thorough development of its side effect profile is needed. Observing, recording, and reporting atypical adverse events and side effec ts are critical to postmarketing surveillance and enhance the clinician's a bility to make rational therapeutic decisions.