Dear Pharmacist:
This letter serves to notify you that the Food and Drug Administration (FDA) requires that a Medication Guide be distributed directly to each patient to whom Cordarone® (amiodarone HCl) Tablets are dispensed. Accordingly, per FDA regulations, a copy of the enclosed Cordarone Tablets Medication Guide must be distributed to each patient who fills a prescription for Cordarone Tablets, effective immediately.
Enclosed are 100 copies of the Cordarone Tablets Medication Guide for distribution to patients. Should you require additional copies of the Cordarone Tablets Medication Guide, you may request copies from Wyeth by calling our Medical Communications Department at 1-800-934-5556. You may also photocopy the enclosed, after confirming that it is the most current version by going to the Wyeth Web site http://www.wyeth.com, clicking on “Products,” and scrolling down to Cordarone® (amiodarone HCl) Tablets, Patient Information or by calling our Medical Communications Department at the number above. Additionally, you may print copies of the Medication Guide from the Wyeth Web site.
Please see the following important boxed Warnings about Cordarone Tablets.
Should you have any questions concerning Cordarone Tablets product information, please call Wyeth at 1-800-934-5556.
In addition, you can send adverse event information directly to Wyeth Global Safety Surveillance and Epidemiology (GSSE) by fax to 610-989-5544 or by mail to GSSE, 500 Arcola Road, Collegeville, PA 19426.
Adverse event information may also be reported to the FDA MedWatch Reporting System by phone (1-800-FDA-1088), fax (1-800-FDA-0178), via the MedWatch Web site at www.fda.gov/medwatch, or by mail (using postage paid form) to MedWatch, HF-2, 5600 Fisher’s Lane, Rockville, MD 20852-9787.
Cordarone® (amiodarone HCl) is intended for use only in patients with the indicated life-threatening arrhythmias because its use is accompanied by substantial toxicity.
Cordarone has several potentially fatal toxicities, the most important of which is pulmonary toxicity (hypersensitivity pneumonitis or interstitial/alveolar pneumonitis) that has resulted in clinically manifest disease at rates as high as 10 to 17% in some series of patients with ventricular arrhythmias given doses around 400 mg/day, and as abnormal diffusion capacity without symptoms in a much higher percentage of patients. Pulmonary toxicity has been fatal about 10% of the time. Liver injury is common with Cordarone, but is usually mild and evidenced only by abnormal liver enzymes. Overt liver disease can occur, however, and has been fatal in a few cases. Like other antiarrhythmics, Cordarone can exacerbate the arrhythmia, e.g., by making the arrhythmia less well tolerated or more difficult to reverse. This has occurred in 2 to 5% of patients in various series, and significant heart block or sinus bradycardia has been seen in 2 to 5%. All of these events should be manageable in the proper clinical setting in most cases. Although the frequency of such proarrhythmic events does not appear greater with Cordarone than with many other agents used in this population, the effects are prolonged when they occur.
Even in patients at high risk of arrhythmic death, in whom the toxicity of Cordarone is an acceptable risk, Cordarone poses major management problems that could be life-threatening in a population at risk of sudden death, so that every effort should be made to utilize alternative agents first.
The difficulty of using Cordarone effectively and safely itself poses a significant risk to patients. Patients with the indicated arrhythmias must be hospitalized while the loading dose of Cordarone is given, and a response generally requires at least one week, usually two or more. Because absorption and elimination are variable, maintenance-dose selection is difficult, and it is not unusual to require dosage decrease or discontinuation of treatment. In a retrospective survey of 192 patients with ventricular tachyarrhythmias, 84 required dose reduction and 18 required at least temporary discontinuation because of adverse effects, and several series have reported 15 to 20% overall frequencies of discontinuation due to adverse reactions. The time at which a previously controlled life-threatening arrhythmia will recur after discontinuation or dose adjustment is unpredictable, ranging from weeks to months. The patient is obviously at great risk during this time and may need prolonged hospitalization. Attempts to substitute other antiarrhythmic agents when Cordarone must be stopped will be made difficult by the gradually, but unpredictably, changing amiodarone body burden. A similar problem exists when Cordarone is not effective; it still poses the risk of an interaction with whatever subsequent treatment is tried. |
Sincerely,
Brenda Cooperstone, MD
Vice President, Global Medical Affairs
Enclosures:
Cordarone Tablets Prescribing Information
Cordarone Tablets Medication Guide
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Safety Summary
