Lanoxin tablet: Difference between revisions
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'''Maintenance dose''': 3.4-5.1 mcg/kg/day once daily. | '''Maintenance dose''': 3.4-5.1 mcg/kg/day once daily. | ||
| | |fdaLIADPed====Heart failure=== | ||
====Loading dose:==== | |||
'''5-10 years old''' | |||
20-45 mcg/kg Administer half the total loading dose initially, | |||
then ¼ the loading dose every 6 to 8 hours twice. | |||
'''>10 year old '''' | |||
10-15 mcg/kg Administer half the total loading dose initially, | |||
then ¼ the loading dose every 6 to 8 hours twice. | |||
====Maintenence dose:==== | |||
'''Less than 10 years old''' | |||
3.2-6.4 mcg/kg/dose twice a day. | |||
'''More than 10 years ''' | |||
3.4-5.1 mcg/kg/day | |||
|offLabePed=====Supraventricular tachycardia, Recurrent; Prophylaxis====<ref name="Pfammatter-1998">{{Cite journal | last1 = Pfammatter | first1 = JP. | last2 = Stocker | first2 = FP. | title = Re-entrant supraventricular tachycardia in infancy: current role of prophylactic digoxin treatment. | journal = Eur J Pediatr | volume = 157 | issue = 2 | pages = 101-6 | month = Feb | year = 1998 | doi = | PMID = 9504781 }}</ref> 0.01 mg/kg orally 3 times daily for the first 2 doses, then 0.0035 mg/kg 3 times daily | |||
<ref name="Sanatani-2012">{{Cite journal | last1 = Sanatani | first1 = S. | last2 = Potts | first2 = JE. | last3 = Reed | first3 = JH. | last4 = Saul | first4 = JP. | last5 = Stephenson | first5 = EA. | last6 = Gibbs | first6 = KA. | last7 = Anderson | first7 = CC. | last8 = Mackie | first8 = AS. | last9 = Ro | first9 = PS. | title = The study of antiarrhythmic medications in infancy (SAMIS): a multicenter, randomized controlled trial comparing the efficacy and safety of digoxin versus propranolol for prophylaxis of supraventricular tachycardia in infants. | journal = Circ Arrhythm Electrophysiol | volume = 5 | issue = 5 | pages = 984-91 | month = Oct | year = 2012 | doi = 10.1161/CIRCEP.112.972620 | PMID = 22962431 }}</ref> | |||
*Fetal tachycardia - Supraventricular tachycardia | *Fetal tachycardia - Supraventricular tachycardia | ||
|contraindications=*Ventricular fibrillation | |contraindications=*Ventricular fibrillation |
Revision as of 20:48, 19 March 2014
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]{{{authorTag}}}
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Disclaimer
Overview
Lanoxin tablet is a Cardiac glycoside drug that is FDA approved for the treatment of heart failure and atrial fibrillation. Adverse reactions include AV block, tachycardia, GI symptoms and visual disturbances.
Adult Indications and Dosage
Pediatric Indications and Dosage
Contraindications
Warnings
Adverse Reactions
Drug Interactions
Use in Specific Populations
Routes and Preparations
IV Compatibility
Overdosage
Pharmacology
Clinical Studies
How Supplied
Images
Patient Information
Patient Information from FDA
Patient Information from NLM
Look-Alike Drug Names
Price
Drug Shortage
Adult Indications and Dosage
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===FDA-Labeled Indications and Dosage (Adult)===
Heart failure
Loading dose"': 10-15 mcg/kg half of dose administered initially, and the other two quarters are given every 6-8 hours twice.
Maintenance dose: 3.4-5.1 mcg/kg/day once daily.
Atrial fibrillation
Loading dose"': 10-15 mcg/kg half of dose administered initially, and the other two quarters are given every 6-8 hours twice.
Maintenance dose: 3.4-5.1 mcg/kg/day once daily.
===Off-Label Use and Dosage (Adult)===
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{{DrugReflist}}Pediatric Indications and Dosage
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===FDA-Labeled Indications and Dosage (Pediatric)===
Heart failure
Loading dose:
5-10 years old
20-45 mcg/kg Administer half the total loading dose initially,
then ¼ the loading dose every 6 to 8 hours twice. >10 year old ' 10-15 mcg/kg Administer half the total loading dose initially, then ¼ the loading dose every 6 to 8 hours twice.
Maintenence dose:
Less than 10 years old 3.2-6.4 mcg/kg/dose twice a day. More than 10 years 3.4-5.1 mcg/kg/day
===Off-Label Use and Dosage (Pediatric)===
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{{DrugReflist}}Contraindications
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===Contraindications===
- Ventricular fibrillation
- Hypersensitivity to digoxin
Warnings
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===Warnings===
Sinus Node Disease and AV Block
Because digoxin slows sinoatrial and AV conduction, the drug commonly prolongs the PR interval. The drug may cause severe sinus bradycardia or sinoatrial block in patients with pre-existing sinus node disease and may cause advanced or complete heart block in patients with pre-existing incomplete AV block. In such patients consideration should be given to the insertion of a pacemaker before treatment with digoxin.
Accessory AV Pathway (Wolff-Parkinson-White Syndrome)
After intravenous digoxin therapy, some patients with paroxysmal atrial fibrillation or flutter and a coexisting accessory AV pathway have developed increased antegrade conduction across the accessory pathway bypassing the AV node, leading to a very rapid ventricular response or ventricular fibrillation. Unless conduction down the accessory pathway has been blocked (either pharmacologically or by surgery), digoxin should not be used in such patients. The treatment of paroxysmal supraventricular tachycardia in such patients is usually direct-current cardioversion.
Use in Patients With Preserved Left Ventricular Systolic Function
Patients with certain disorders involving heart failure associated with preserved left ventricular ejection fraction may be particularly susceptible to toxicity of the drug. Such disorders include restrictive cardiomyopathy, constrictive pericarditis, amyloid heart disease, and acute cor pulmonale. Patients with idiopathic hypertrophic subaortic stenosis may have worsening of the outflow obstruction due to the inotropic effects of digoxin. Digoxin should generally be avoided in these patients, although it has been used for ventricular rate control in the subgroup of patients with atrial fibrillation.
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Use in Specific Populations
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===Pregnancy===
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There is no FDA guidance on usage of {{BASEPAGENAME}} in women who are pregnant.
:'''[[Pregnancy category#Australia|Pregnancy Category (AUS)]]'''
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of {{BASEPAGENAME}} in women who are pregnant.
===Labor and Delivery===
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===Nursing Mothers===
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===Pediatric Use===
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===Geriatic Use===
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===Gender===
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===Race===
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===Renal Impairment===
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===Hepatic Impairment===
There is no FDA guidance on the use of {{BASEPAGENAME}} in patients with hepatic impairment.
===Females of Reproductive Potential and Males===
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===Immunocompromised Patients===
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Overdose
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'''Please contact the National Poison Help hotline (1-800-222-1222) immediately if there is suspicion of drug poisoning or overdose.'''
===Overdose===
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{{DrugReflist}}Pharmacology
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===Mechanism of Action===
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===Structure===
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===Pharmacodynamics===
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===Pharmacokinetics===
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===Nonclinical Toxicology===
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