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| (TOE-cane-ide HIGH-droe-KLOR-ide) |
| Tonocard |
| Class: Antiarrhythmic |
Action Produces dose-dependent decreases in sodium and potassium conductance resulting in decrease in myocardial cell excitability.
Indications Treatment of life-threatening ventricular arrhythmias. Unlabeled use(s): Treatment of myotonic dystrophy and trigeminal neuralgia.
Contraindications Hypersensitivity to tocainide or amidetype local anesthetics; second-or third-degree atrioventricular block in absence of artificial ventricular pacemaker.
ADULTS: PO 400 mg q 8 hr initially. Maintenance: 1200–1800 mg/day in 3 divided doses.
Cimetidine: May decrease tocainide bioavailability and peak concentration. Rifampin: May decrease tocainide bioavailability and elimination half-life; may increase tocainide oral clearance.
Lab Test Interferences None well documented.
CV: Increased ventricular arrhythmias; PVCs; CHF and progression of CHF; tachycardia; hypotension; bradycardia; palpitations; chest pain; conduction disorders. CNS: Dizziness; vertigo; paresthesias; tremor; nervousness; anxiety; confusion; eadache; seizures. DERM: Diaphoresis; systemic lupus erythematosus; rash; skin lesion. EENT: Visual disturbances; nystagmus; tinnitus; hearing loss. GI: Nausea; vomiting; anorexia; diarrhea. HEMA: Anemia; leukopenia; thrombocytopenia; aplastic anemia; agranulocytosis. HEPA: Increased LFT result; hepatitis; jaundice. RESP: Respiratory arrest; pulmonary fibrosis; pulmonary edema; dyspnea. OTHER: Arthritis or arthralgia; myalgia; increased creatine phosphokinase.
Pregnancy: Category C. Lactation: Excreted in breast milk. Children: Safety and efficacy not established. Blood dyscrasias: Have occurred, with some fatalities. Blood tests are required weekly for first 3 mo, and frequently thereafter. Cardiac effects: Use drug with caution and in lower doses in patients with CHF or reduced cardiac output. Hypokalemia: Should be corrected prior to initiation of tocainide therapy to ensure efficacy. Proarrhythmia: Tocainide has proarrhythmic effect. Pulmonary fibrosis: Has occurred, as have other pulmonary complications. Promptly report any pulmonary symptoms. Renal or hepatic impairment: Use drug with caution in patients with renal or hepatic impairment. Dosage reduction and modified dosing intervals may be required.
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