XENAZINE®
(tetrabenazine) Tablets

• Xenazine® is a monoamine depletor for oral administration.
• Xenazine is available as a 12.5 or 25 mg tablet.

                                                                                                                                            

Indications and Usage:

Xenazine is indicated for the treatment of chorea associated with Huntington’s disease.

Important Safety Information:

Xenazine is also contraindicated in patients who have impaired hepatic function or are taking monoamine oxidase inhibitors or reserpine. At least 20 days should elapse after stopping reserpine before starting Xenazine.

The need for therapy should be evaluated on an ongoing basis with the patient’s doctor. Xenazine should be titrated slowly over several weeks for a dose that is appropriate for each patient. Before a dose greater than 50 mg is administered, the patient’s CYP2D6 metabolizer status should be determined.

Neuroleptic malignant syndrome (NMS), akathisia, agitation, parkinsonism, dysphagia, and QT prolongation–related arrhythmias have been reported with use of Xenazine. Xenazine should not be used in combination with drugs known to prolong QTc (which in certain circumstances can lead to torsades de pointes and/or sudden death), in patients with congenital long QT syndrome, or in patients with a history of cardiac arrhythmias. A potentially irreversible syndrome of involuntary, dyskinetic movements called tardive dyskinesia (TD) may develop in patients treated with neuroleptic drugs.   If signs and symptoms of TD appear in a patient treated with Xenazine, drug discontinuation should be considered.  Adverse reactions associated with Xenazine, such as QTc prolongation, NMS, and extrapyramidal disorders, may be exaggerated by concomitant use of dopamine antagonists.

Xenazine elevates serum prolactin concentrations. Xenazine may induce sedation and somnolence (sleepiness or drowsiness) and may impair the ability to drive or operate dangerous machinery.

Some adverse events such as depression, fatigue, insomnia, sedation/somnolence, parkinsonism, and akathisia may be dose-dependent. If the adverse effect does not resolve or decrease, consideration should be given to lowering or discontinuing Xenazine. The most commonly reported adverse events with Xenazine compared to placebo were sedation/somnolence (31% vs 3%), fatigue (22% vs 13%), insomnia (22% vs 0%), depression (19% vs 0%), akathisia (19% vs 0%), anxiety (15% vs 3%), and nausea (13% vs 7%).

For more information, please see Full Prescribing Information including Boxed Warning, or go to www.xenazineusa.com.

® Xenazine is a registered trademark of Biovail Laboratories International (Barbados)S.R.L.