Classes
DEA Class; Rx
Common Brand Names; Corlanor
- I(f) Current Inhibitors
Description
Used for the treatment of stable symptomatic heart failure
Contraindicated when used in combination with strong CYP3A4 inhibitors
Indications
Indicated to reduce the risk of hospitalization for worsening heart failure in patients with stable, symptomatic chronic heart failure with LVEF ≤35%, who are in sinus rhythm with resting heart rate ≥70 bpm and either are on maximally tolerated doses of beta-blockers or have a contraindication to beta-blocker use
Contraindications
Acute decompensated heart failure
Clinically significant hypotension
Sick sinus syndrome, sinoatrial block, or third-degree AV block (unless a functioning demand pacemaker is present)
Clinically significant bradycardia
Severe hepatic impairment
Pacemaker dependence (heart rate maintained exclusively by the pacemaker)
Concomitant use of strong CYP3A4 inhibitors
Adverse Effects
Bradycardia (10%)
Hypertension or increased blood pressure (8.9%)
Atrial fibrillation (8.3%)
Luminous phenomena (phosphenes) or visual brightness (2.8%)
Syncope, hypotension
Angioedema, erythema, rash, pruritus, urticaria
Vertigo, diplopia, visual impairment
Torsade de pointes, ventricular fibrillation, ventricular tachycardia
Warnings
Increases the risk of atrial fibrillation; regularly monitor cardiac rhythm and discontinue drug if atrial fibrillation develops
May cause fetal toxicity when administered to a pregnant woman; inform women of childbearing potential to use effective contraception
Pregnancy and Lactation
There are no adequate and well-controlled studies in pregnant women to inform any drug-associated risks
Advise females of childbearing potential to use effective contraception
Unknown if distributed in human breast milk
Maximum Dosage
7.5 mg PO twice daily.
7.5 mg PO twice daily.
Weighing 40 kg or more: 7.5 mg PO twice daily.
Weighing less than 40 kg: 0.3 mg/kg/dose PO twice daily (Max: 7.5 mg/dose).
Weighing 40 kg or more: 7.5 mg PO twice daily.
Weighing less than 40 kg: 0.3 mg/kg/dose PO twice daily (Max: 7.5 mg/dose).
6 to 11 months: 0.2 mg/kg/dose PO twice daily.
1 to 5 months: Safety and efficacy have not been established.
Safety and efficacy have not been established.
How supplied
Ivabradine
tablet
- 5mg (scored and can be divided into equal halves to provide a 2.5-mg dose)
- 7.5mg
oral solution
- 5mg/5mL