Brand Name

Corlanor

Generic Name
Ivabradine
View Brand Information
FDA approval date: April 20, 2015
Classification: Hyperpolarization-activated Cyclic Nucleotide-gated Channel Blocker
Form: Tablet, Solution

What is Corlanor (Ivabradine)?

For people living with chronic heart failure, every breath and heartbeat can feel like hard work. Fatigue, shortness of breath, and limits on physical activity often become part of daily life. Corlanor (ivabradine) is a medication designed to help patients with certain types of heart failure manage these symptoms, reduce hospitalizations, and improve their overall quality of life. 

Corlanor is a heart rate–lowering medication that belongs to a class of drugs known as hyperpolarization-activated cyclic nucleotide-gated (HCN) channel blockers, sometimes called If channel inhibitors. Unlike traditional beta-blockers, which affect several aspects of heart function, Corlanor specifically targets the natural pacemaker of the heart to slow its rhythm without reducing the strength of each heartbeat. 

Approved by the U.S. Food and Drug Administration (FDA) in 2015, Corlanor is a relatively new addition to the tools cardiologists use to manage chronic heart failure with reduced ejection fraction (HFrEF). It’s often prescribed alongside standard therapies such as beta-blockers, ACE inhibitors, or ARBs to provide additional heart rate control and symptom relief. 

What does Corlanor do? 

Corlanor is used to treat adults with chronic heart failure who have a stable heart rhythm (sinus rhythm) and a resting heart rate of 70 beats per minute or higher, despite being on maximum tolerated beta-blocker therapy. It helps the heart work more efficiently by slowing down its rate, giving it more time to fill with blood before pumping it out to the body. 

By improving the timing and efficiency of each heartbeat, Corlanor can reduce symptoms like fatigue, dizziness, and shortness of breath. It also helps lower the risk of hospitalization due to worsening heart failure (FDA, 2024). 

In clinical trials, such as the SHIFT study, patients taking ivabradine in addition to standard heart failure treatments experienced a significant reduction in hospitalizations and disease progression compared with those receiving placebo. This means Corlanor doesn’t just improve day-to-day comfort, it may also help people live longer and stay healthier. 

How does Corlanor work? 

Corlanor works by selectively blocking the “funny” current (If current) in the sinoatrial (SA) node, the part of the heart that controls its natural rhythm. This electrical current regulates how quickly the heart beats. By slowing this current, Corlanor reduces the heart rate without affecting the heart’s ability to contract or the blood pressure. 

In simpler terms, Corlanor helps the heart beat more slowly and efficiently. When the heart rate is lowered, the heart muscle has more time to fill with blood before each contraction. This increases oxygen delivery to the body while reducing the workload on the heart. 

This mechanism is especially useful for patients with chronic heart failure because a persistently fast heart rate can strain an already weakened heart. By controlling heart rhythm, Corlanor supports better long-term heart function and symptom management. 

Corlanor side effects 

Most patients tolerate Corlanor well, but as with any prescription medication, side effects can occur. These are generally mild and may improve over time. 

Common side effects include: 

  • Slow heartbeat (bradycardia) 
     
  • High blood pressure 
     
  • Temporary visual disturbances (bright spots or flashing lights, called phosphenes
     
  • Fatigue or dizziness 

Serious side effects (less common): 

  • Fainting or very slow heart rate 
     
  • Irregular heartbeats (atrial fibrillation) 
     
  • Severe dizziness or shortness of breath 
     
  • Signs of an allergic reaction (rash, swelling, or difficulty breathing) 

Visual effects, such as seeing brief flashes of light, are unique to Corlanor and usually occur within the first two months of treatment. These are caused by ivabradine’s mild effects on the retina but are typically temporary and reversible. 

Corlanor is unsuitable for patients with severe liver disease, very low blood pressure, slow resting heart rate, or certain unstable irregular heart rhythms (like atrial fibrillation). Immediately contact a doctor for chest pain, fainting, or worsening heart failure symptoms (e.g., swelling, breathlessness). 

Corlanor dosage 

Corlanor is taken by mouth in tablet form, usually twice daily with meals. The medication works best when taken consistently at the same times each day. Doctors determine and adjust your dose based on your resting heart rate and health, aiming for 50-60 bpm. 

Regular heart rate monitoring (via checkups or ECGs) is crucial during treatment to ensure effectiveness and prevent a dangerously low heart rate. Patients with liver problems or light sensitivity may require dose adjustments or extra precautions.  

While generally safe for older adults, closer monitoring may be needed due to age-related changes in heart rhythm or metabolism. 

Does Corlanor have a generic version? 

Yes. As of 2022, the FDA has approved a generic version of Corlanor, available under the generic name ivabradine. The generic medication is therapeutically equivalent to the brand-name version, meaning it contains the same active ingredient and provides the same clinical benefits and safety profile. 

Corlanor and generic ivabradine are available as tablets and oral solutions. Generic ivabradine offers a cost-effective and equally effective alternative for managing heart failure. 

Conclusion 

Corlanor (ivabradine) is a valuable treatment for adults with chronic heart failure who need additional heart rate control beyond standard medications. By slowing the heart’s rhythm without lowering blood pressure or heart strength, it helps the heart pump more efficiently and reduces the risk of hospitalizations. 

Most people tolerate Corlanor well, and side effects are typically mild and manageable. Regular monitoring with your healthcare team ensures safe and effective treatment. While not a cure, Corlanor significantly helps heart failure patients live longer, feel better, and stay active. Following your doctor’s guidance and treatment plan is key to better heart health. 

References 

  1. U.S. Food and Drug Administration (FDA). (2024). Corlanor (ivabradine) prescribing information. Retrieved from https://www.accessdata.fda.gov 
     
  1. Mayo Clinic. (2024). Ivabradine (oral route) drug information. Retrieved from https://www.mayoclinic.org 
     
  1. MedlinePlus. (2024). Ivabradine: Uses, dosage, and side effects. National Library of Medicine. Retrieved from https://medlineplus.gov 
     
  1. National Institutes of Health (NIH). (2024). Heart failure treatment: Beta-blockers, ACE inhibitors, and ivabradine. Retrieved from https://www.nih.gov 
     

Approved To Treat

Save this treatment for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms

Related Clinical Trials

Left Bundle Branch Pacing as Initial Therapy in Patients With Non-ischemic Heart Failure and Left Bundle Branch Block (LIT-HF Study)

Summary: The present study will recruit 50 symptomatic non-ischemic cardiomyopathy (NICM) patients with left ventricular ejection fraction (LVEF) below 35% and complete left bundle branch block (CLBBB), who have not received complete guideline-directed medical therapy (GDMT). Each patient was randomized to 2 groups, GDMT or left bundle branch pacing combined with GDMT (LBBP+GDMT) as initial therapy and was...

Effect Of Atenolol Versus Ivabradine On Heart Rate Variability In Treatment Resistant Schizophrenia Patients On Clozapine With Tachycardia: A Randomized Control Trial.

Summary: Clozapine is the only drug approved for Treatment Resistant Schizophrenia. However, it has been associated with many adverse drug reactions including agranulocytosis, myocarditis, sialorrhea, constipation, orthostasis, tachycardia. There are many factors that have impacted the use of clozapine in TRS patients including physician hesitation, patient denial, stopping of drug due to Adverse drug reac...

A Multicenter, Prospective, Randomized, Placebo-controlled, Double-blind, Multi-arm, Multi-stage Clinical Trial of Ivabradine for Heart Rate Control In Septic Shock

Summary: Septic shock is a major health problem, with several million cases annually worldwide and a mortality approaching 45%. Tachycardia is associated with excess mortality during septic shock. This pejorative effect could be related to the increase in cardiac metabolic demand, impaired cardiac diastolic function, and/or poorer tolerance of administered exogenous catecholamines. Recent studies suggest t...

Brand Information

Corlanor (ivabradine)
1DOSAGE FORMS AND STRENGTHS
Corlanor Tablets
5 mg: salmon-colored, oval-shaped, film-coated tablet, functionally scored on both edges, debossed with “5” on one face and bisected on the other face. The tablet is scored and can be divided into equal halves to provide a 2.5 mg dose.
7.5 mg: salmon-colored, triangular-shaped, film-coated tablet debossed with “7.5” on one face and plain on the other face.
Corlanor Oral Solution
Corlanor 5 mg/5 mL (1 mg/mL) oral solution is a colorless liquid in an opaque, plastic, ampule containing 5 mg of Corlanor in 5 mL of liquid.
2CONTRAINDICATIONS
Corlanor is contraindicated in patients with:
• Acute decompensated heart failure
• Clinically significant hypotension
• Sick sinus syndrome, sinoatrial block or 3
• Clinically significant bradycardia 
• Severe hepatic impairment 
• Pacemaker dependence (heart rate maintained exclusively by the pacemaker) 
• Concomitant use of strong cytochrome P450 3A4 (CYP3A4) inhibitors
3ADVERSE REACTIONS
Clinically significant adverse reactions that appear in other sections of the labeling include:
  • Atrial Fibrillation
  • Bradycardia and Conduction Disturbances
3.1Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
Adult Patients with Heart Failure
In SHIFT, safety was evaluated in 3,260 patients treated with Corlanor and 3,278 patients given placebo. The median duration of Corlanor exposure was 21.5 months.
The most common adverse drug reactions in the SHIFT trial are shown in Table 2 
Luminous Phenomena (Phosphenes)
Phosphenes are phenomena described as a transiently enhanced brightness in a limited area of the visual field, halos, image decomposition (stroboscopic or kaleidoscopic effects), colored bright lights, or multiple images (retinal persistency). Phosphenes are usually triggered by sudden variations in light intensity. Corlanor can cause phosphenes, thought to be mediated through Corlanor’s effects on retinal photoreceptors 
Pediatric Patients with Heart Failure
The safety of Corlanor in pediatric patients 6 months to less than 18 years of age is based on a clinical trial
3.2Postmarketing Experience
Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to estimate their frequency reliably or establish a causal relationship to drug exposure.
The following adverse reactions have been identified in adults during post-approval use of Corlanor: syncope, hypotension, torsade de pointes, ventricular fibrillation, ventricular tachycardia, angioedema, erythema, rash, pruritus, urticaria, vertigo, and diplopia, and visual impairment.
4OVERDOSAGE
Overdose may lead to severe and prolonged bradycardia. In the event of bradycardia with poor hemodynamic tolerance, temporary cardiac pacing may be required. Supportive treatment, including intravenous (IV) fluids, atropine, and intravenous beta-stimulating agents such as isoproterenol, may be considered.
5DESCRIPTION
Corlanor (ivabradine) tablets and oral solution contains ivabradine as the active pharmaceutical ingredient. Ivabradine is a hyperpolarization-activated cyclic nucleotide-gated channel blocker that reduces the spontaneous pacemaker activity of the cardiac sinus node by selectively inhibiting the I
The chemical name for ivabradine hydrochloride is 3-(3-{[((7
Figure 1. Chemical Structure of Ivabradine
Figure 1. Chemical Structure of Ivabradine
Tablets
Corlanor tablets are supplied in 5 mg and 7.5 mg tablets for oral administration. The tablets contain 5 mg and 7.5 mg of ivabradine, as the active ingredient, equivalent to 5.39 mg and 8.09 mg of ivabradine hydrochloride, respectively. The tablets contain the following inactive ingredients: colloidal silicon dioxide, glycerol, hypromellose, lactose monohydrate, magnesium stearate, maize starch, maltodextrin, polyethylene glycol 6000, red iron oxide, titanium dioxide, and yellow iron oxide.
Oral Solution
Corlanor 5 mg/5 mL (1 mg/mL) oral solution is formulated as a sterile, preservative-free, colorless solution for oral administration. Each 5 mL ampule contains 5 mg of ivabradine, equivalent to 5.39 mg ivabradine hydrochloride, as the active ingredient. The solution contains the following inactive ingredients: maltitol and water.
6HOW SUPPLIED/STORAGE AND HANDLING
Tablets:
Corlanor (ivabradine) 5 mg tablets are formulated as salmon-colored, oval-shaped, film-coated tablets functionally scored on both edges, marked with “5” on one face and bisected on the other face. They are supplied as follows:
  • Bottles of 60 tablets with child-resistant closure (NDC 55513-800-60)
Corlanor (ivabradine) 7.5 mg tablets are formulated as salmon-colored, triangular-shaped, film-coated tablets debossed with “7.5” on one face and plain on the other face.  They are supplied as follows:
  • Bottles of 60 tablets with child-resistant closure (NDC 55513-810-60)
Oral Solution:
Corlanor (ivabradine) oral solution is a colorless liquid supplied in an opaque, low density polyethylene (LDPE) plastic ampule. Each 5 mL ampule is individually packaged in a child-resistant foil pouch and supplied in cartons containing 28 foil pouches. Corlanor oral solution is supplied as 5 mg/5 mL (1 mg/mL) (NDC 55513-813-01).
Storage
Store Corlanor tablets and oral solution at 25°C (77°F); excursions permitted to 15°C - 30°C (59°F - 86°F)
7PATIENT COUNSELING INFORMATION
Advise the patient to read the FDA-approved patient labeling
  • Fetal Toxicity
    Advise pregnant women of the potential risks to a fetus.
    Advise females of reproductive potential to use effective contraception and to notify their healthcare provider with a known or suspected pregnancy [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1), (8.3)]
  • Low Heart Rate
    Advise patients to report significant decreases in heart rate or symptoms such as dizziness, fatigue, or hypotension [see Warnings and Precautions (5.3)].
  • Atrial Fibrillation
    Advise patients to report symptoms of atrial fibrillation, such as heart palpitations or racing, chest pressure, or worsened shortness of breath [see Warnings and Precautions (5.2)].
  • Phosphenes
    Advise patients about the possible occurrence of luminous phenomena (phosphenes). Advise patients to use caution if they are driving or using machines in situations where sudden changes in light intensity may occur, especially when driving at night. Advise patients that phosphenes may subside spontaneously during continued treatment with Corlanor [see Adverse Reactions (6.1)].
  • Drug Interactions
    Advise patients to avoid ingestion of grapefruit juice and St. John’s wort [see Drug Interactions(7.1)].
  • Intake with Food
    Advise patients to take Corlanor twice daily with food [see Dosage and Administration (2)].
  • Oral Solution
    Advise parents/caregivers on preparation and administration instructions including the use of a calibrated oral syringe and a medicine cup (provided by the pharmacy) to avoid dosing errors [see Dosage and Administration (2.2)].
    Advise parents/caregivers that the oral solution should not be administered by the child.
    Advise parents/caregivers to not double up doses (e.g., if patient spits out the drug or caregiver forgets to give the drug at the prescribed time).
    Advise parents/caregivers to throw away the unused product remaining in the cup immediately after drawing up the prescribed dose in the syringe.
Corlanor
Manufactured by:
Amgen Inc.
One Amgen Center Drive
Thousand Oaks, California 91320-1799
Patent:
© 2015, 2017, 2019, 2021 Amgen Inc. All rights reserved.
8PRINCIPAL DISPLAY PANEL - 5 mg Tablet Bottle Label
AMGEN
NDC 55513-800-60
5
Corlanor
Each tablet contains 5 mg ivabradine equivalent
Rx Only
60
PRINCIPAL DISPLAY PANEL - 5 mg Tablet Bottle Label
9PRINCIPAL DISPLAY PANEL - 7.5 mg Tablet Bottle Label
AMGEN
NDC 55513-810-60
7.5
Corlanor
Each tablet contains 7.5 mg ivabradine equivalent
Rx Only
60
PRINCIPAL DISPLAY PANEL - 7.5 mg Tablet Bottle Label
10PRINCIPAL DISPLAY PANEL - 5 mg/5 mL Ampule Carton
NDC 55513-813-28
Caregiver/Patient: Read the included "Instructions for Use" insert to be sure you prepare and administer the correct dose.
AMGEN
ATTENTION
Corlanor
5 mg/5 mL (1 mg/mL)
Sterile Oral Solution in an Ampule
Rx Only
Contains 28
PRINCIPAL DISPLAY PANEL - 5 mg/5 mL Ampule Carton