- March 15, 2022
- Newsletter
- 617-430-5616
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Brand Name :
Corvert
Synonyms :
ibutilide
Class :
Antidysrhythmic, III
Dosage Forms & Strengths
Injectable solution
0.1mg/ml
>60 kg: 1 mg (one vial) intravenous infusion. May repeat after ten minutes when necessary
<60 kg: 0.01 mg/kg (0.1 mL/kg) intravenous infusion. May repeat after ten minutes when necessary
Safety and Efficacy not established
Refer adult dosing
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging Class III Antiarrhythmics
may increase the QTc prolonging effect of QT-prolonging agents
It may enhance QTc interval when combined with erythromycin stearate
It may enhance QTc interval when combined with perphenazine
It may enhance QTc interval when combined with epinephrine
when both drugs are combined, there may be an increase in qtc interval
may increase the QTc prolonging effect of QT-prolonging agents
when both drugs are combined, there may be an increased risk or severity of QTC prolongation
QTc interval is increased both by lenvatinib and ibutilide
both lapatinib and ibutilide increase the QTc interval
ibutilide and gilteritinib, when used in combination, increase the QTc interval
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
may increase the QTc prolonging effect of QT-prolonging agents
Actions and Spectrum:
Frequency defined
1-10%
Bradycardia (2%)
Hypotension (2%)
QTc interval prolongation (<2%)
Headache (4%)
HTN (2%)
Palpitations (2%)
Nausea (>2%)
<1%
Erythematous bullous lesions
Renal failure
Ventricular tachycardia
Heart block
Heart failure
Nodal arrhythmia
Syncope
Torsades de pointes
Contraindications/caution:
Contraindications:
Caution:
Pregnancy consideration: Insufficient data available
Lactation:
Pregnancy category:
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.
Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women.
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.
Category N: There is no data available for the drug under this category
Pharmacology:
ibutilide works by blocking potassium channels in the heart, which prolongs the action potential duration and refractory period in the atrial and ventricular myocardium. This results in an antiarrhythmic effect by helping to prevent the reentry of abnormal electrical signals in the heart
Pharmacodynamics:
ibutilide has a relatively narrow therapeutic index, meaning that the therapeutic dose is close to the toxic dose. The drug can cause prolongation of the QT interval on the electrocardiogram, which can lead to a potentially life-threatening arrhythmia called torsades de pointes. Therefore, patients receiving ibutilide should be closely monitored for changes in their QT interval and other potential adverse effects.
Pharmacokinetics:
Absorption
ibutilide is administered intravenously and is rapidly and completely absorbed following injection.
Distribution
The volume of distribution of ibutilide is approximately 7 L/kg, suggesting that the drug is widely distributed throughout the body. The plasma protein binding of ibutilide is about 40-50%.
Metabolism
ibutilide is metabolized by the liver through the cytochrome P450 enzyme system, predominantly by the CYP3A4 isoform, into inactive metabolites.
Elimination and Excretion
The elimination half-life of ibutilide is approximately 6 hours. The drug is excreted primarily in the urine, with approximately 50-60% of the dose being excreted unchanged in the urine. The remaining portion of the drug is excreted in feces.
Administration:
ibutilide is administered intravenously (IV) in a hospital or clinical setting. It is typically given as a single dose over 10 minutes. The recommended dose of ibutilide is based on the patient’s body weight and cardiac function and is usually between 0.01 and 0.025 mg/kg
Patient information leaflet
Generic Name: ibutilide
Pronunciation: [ eye-BUE-til-ide ]
Why do we use ibutilide?