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Medsafe Pharmacovigilance Team
Web site: June 2005
Prescriber Update 2005;26(1):9
Prescribers are reminded that thioridazine is a third-line antipsychotic agent and should only be prescribed in patients for whom the therapeutic benefits clearly outweigh the risk of arrhythmia from QT-prolongation.
Thioridazine (Aldazine®, Melleril®*) increases the risk of arrhythmia from QT-prolongation. Consequently, the Medicines Adverse Reactions Committee (MARC) recommended changes to how thioridazine is prescribed in New Zealand. The following advice was issued in June 2001 (see www.medsafe.govt.nz/profs/PUarticles/thioridazine.htm), which the MARC would like to reiterate.
Thioridazine is contraindicated in the following circumstances, all of which are risk factors for arrhythmia:
Thioridazine should be initiated only by a specialist and only as third-line therapy. In addition, the following precautions should be observed for new patients:
For all patients currently taking thioridazine:
Any children taking thioridazine should also have their therapy reviewed by a specialist. If thioridazine discontinuation is necessary, gradually reduce the dose over a period of one month and concurrently introduce alternative medication. Specialist supervision may be advisable for the withdrawal process.
* Novartis has advised that from 1 July 2005 supplies of Melleril will no longer be available.
Competing interests (authors): none declared.