1% to 10%: Gastrointestinal: Anorexia, nausea, vomiting
<1% (Limited to important or life-threatening): Sinus bradycardia, AV block, SA block, atrial or nodal ectopic beats, ventricular arrhythmia, bigeminy, trigeminy, atrial tachycardia with AV block, drowsiness, headache, fatigue, lethargy, vertigo, disorientation, hyperkalemia with acute toxicity, feeding intolerance, abdominal pain, diarrhea, neuralgia, blurred vision, halos, yellow or green vision, diplopia, photophobia, flashing lights
Symptoms of acute overdose: Vomiting, hyperkalemia, sinus bradycardia, S-A arrest and AV block are common, ventricular tachycardia, and fibrillation may occur
Chronic intoxication: Visual disturbances, weakness, sinus bradycardia, atrial fibrillation with slowed ventricular response, and ventricular arrhythmias
After GI decontamination, treat hyperkalemia if >5.5 mEq/L with sodium bicarbonate and glucose with insulin or Kayexalate®. Treat bradycardia or heart block with atropine or pacemaker and other arrhythmias with conventional antiarrhythmics. Use Digibind® for severe hyperkalemia, symptomatic arrhythmias unresponsive to other drugs, and for prophylactic treatment in massive overdose.
Amiloride may reduce the inotropic response to digitoxin.
Amiodarone reduces renal and nonrenal clearance of digitoxin and may have additive effects on heart rate.
Beta-blocking agents (propranolol) may have additive effects on heart rate.
Calcium preparations: Rare cases of acute digitalis glycoside toxicity have been associated with parental calcium (bolus) administration.
Cholestyramine, colestipol, kaolin-pectin may reduce digitoxin absorption.
CYP3A4 inducers: CYP3A4 inducers may decrease the levels/effects of digitoxin. Example inducers include aminoglutethimide, carbamazepine, nafcillin, nevirapine, phenobarbital, phenytoin, and rifamycins.
CYP3A4 inhibitors: May increase the levels/effects of digitoxin. Example inhibitors include azole antifungals, ciprofloxacin, clarithromycin, diclofenac, doxycycline, erythromycin, imatinib, isoniazid, nefazodone, nicardipine, propofol, protease inhibitors, quinidine, and verapamil.
Levothyroxine (and other thyroid supplements) may decrease digitoxin blood levels.
Moricizine may increase the toxicity of digitalis glycosides (mechanism undefined).
Propafenone increases digoxin blood levels. Effects may also occur with digitoxin. Monitor closely.
Propylthiouracil and methimazole may increase digitoxin blood levels by reducing thyroid hormone.
Quinidine increases digitoxin blood levels substantially; monitor blood levels/effect closely. Other related agents (hydroxychloroquine, quinine) should be used with caution.
Verapamil, diltiazem, bepridil, and nitrendipine increase digoxin concentrations, and may have similar effect on digitoxin. Other calcium channel blocking agents do not appear to share this effect.
Drugs which cause hypokalemia (thiazide and loop diuretics, amphotericin B): Hypokalemia may potentiate toxicity of digitalis glycosides.
These medications have been associated with reduced blood levels of digitalis glycosides which appear to be of limited clinical significance: Aminoglutethimide, antacids (magnesium- and aluminum-containing), sucralfate, sulfasalazine, ticlopidine.
These medications have been associated with increased digitalis glycoside blood levels which appear to be of limited clinical significance: Famciclovir, flecainide, ibuprofen, itraconazole, cimetidine, famotidine, fluoxetine, nefazodone, omeprazole, ranitidine, trimethoprim.
Absorption: 90% to 100%
Distribution: Vd: 7 L/kg
Protein binding: 90% to 97%
Metabolism: Hepatic (50% to 70%)
Half-life elimination: 7-8 days
Time to peak: 8-12 hours
Excretion: Urine and feces (30% to 50% as unchanged drug)
Children: Doses are very individualized; when recommended, digitalizing dose is as follows:
<1 year: 0.045 mg/kg
1-2 years: 0.04 mg/kg
>2 years: 0.03 mg/kg which is equivalent to 0.75 mg/m2
Maintenance: Approximately 1/10 of the digitalizing dose
Adults: Oral:
Rapid loading dose: Initial: 0.6 mg followed by 0.4 mg and then 0.2 mg at intervals of 4-6 hours
Slow loading dose: 0.2 mg twice daily for a period of 4 days followed by a maintenance dose
Maintenance: 0.05-0.3 mg/day
Most common dose: 0.15 mg/day
Dosing adjustment in renal impairment: Clcr<10 mL/minute: Administer 50% to 75% of normal dose.
Hemodialysis: Not dialyzable (0% to 5%)
Dosing adjustment in hepatic impairment: Dosage reduction is necessary in severe liver disease.
Baciewicz AM, Isaacson ML, and Lipscomb GL, "Cholestyramine Resin in the Treatment of Digitoxin Toxicity,"Drug Intell Clin Pharm, 1983, 17(1):57-9.
Hess T, Riesen W, Scholtysik G, et al, "Digitoxin Intoxication With Severe Thrombocytopenia: Reversal by Digoxin-Specific Antibodies,"Eur J Clin Invest, 1983, 13(2):159-63.
Nolan PE and Mooradian AD, "Digoxin," Bressler R and Katz MD eds, Geriatric Pharmacology, New York, NY: McGraw-Hill, 1993, 7:151-63.
Park GD, Goldberg MJ, Spector R, et al, "The Effects of Activated Charcoal on Digoxin and Digitoxin Clearance,"Drug Intell Clin Pharm, 1985, 19(12):937-41.
Taboulet P, Baud FJ, Bismuth C, et al, "Acute Digitalis Intoxication - Is Pacing Still Appropriate?"Clin Toxicol, 1993, 31:261-73.