Product image of Ivacorlan (Ivabradine Oxalate) supplied by GNH India

Ivacorlan

Active Ingredient:
Ivabradine Oxalate
Origin:
EU

Ivacorlan (Ivabradine Oxalate)

Ivabradine, the active ingredient in Ivacorlan, is a If channel inhibitor presented as an oral tablet for oral use. It reduces heart rate and is indicated for patients with chronic stable angina and for those with heart failure with reduced ejection fraction. By selectively inhibiting the funny current in the sinoatrial node, it lowers heart rate without decreasing myocardial contractility, helping to alleviate anginal symptoms and improve cardiac efficiency.

GNH India supplies Ivacorlan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

G.L. Pharma Gmbh

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Indications & Clinical Uses

Ivacorlan is used in cardiovascular conditions that benefit from heart‑rate reduction.

  • Chronic stable angina: improves exercise tolerance and reduces the frequency of angina attacks.
  • Heart failure with reduced ejection fraction: lowers heart rate, contributing to better ventricular remodeling and reduced risk of hospitalization.
  • Stable angina pectoris: decreases the number of chest pain episodes during daily activities.

How It Works

  • Ivabradine selectively binds to the HCN (hyperpolarization‑activated cyclic nucleotide‑gated) channels that generate the funny (If) current in the sinoatrial node. Inhibition of this current slows depolarisation of pacemaker cells, producing a dose‑dependent reduction in heart rate while preserving myocardial contractility and blood pressure, thereby improving cardiac efficiency in angina and heart‑failure patients.

Side Effects

Adverse reactions may occur with Ivacorlan and are categorized by frequency.

Common Side Effects

  • Bradycardia: heart rate slower than expected.
  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo.
  • Fatigue or general weakness.

Serious or Rare Side Effects

  • Severe bradycardia requiring medical intervention.
  • Atrial fibrillation or other significant arrhythmias.
  • Symptomatic hypotension.
  • High‑grade atrioventricular block.
  • Severe visual impairment or persistent photopsia.
  • Allergic reactions such as rash, angioedema, or anaphylaxis.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Heart‑rate monitoring: ensure baseline rate is ≥60 bpm before starting.
  • Hepatic function: avoid in patients with severe hepatic impairment.
  • Concomitant bradycardic agents: use caution when combined with beta‑blockers, digoxin, or calcium‑channel blockers.
  • Sick‑sinus syndrome or AV block: contraindicated unless a pacemaker is present.
  • CYP3A4 inhibitors: assess potential for increased plasma levels.
  • Store below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Ivacorlan may interact with other medicines, requiring attention to the level of risk.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): can markedly increase ivabradine exposure.
  • Concurrent use with other heart‑rate‑lowering drugs (beta‑blockers, digoxin, non‑dihydropyridine calcium‑channel blockers): may cause severe bradycardia.
  • Pacemaker‑dependent patients receiving ivabradine without appropriate device settings.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., erythromycin, clarithromycin): may raise plasma levels.
  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy.
  • Drugs that prolong QT interval (e.g., amiodarone, sotalol): monitor ECG for additive effects.

Frequently Asked Questions

Ivacorlan contains ivabradine and is prescribed to lower heart rate in patients with chronic stable angina and in those with heart failure with reduced ejection fraction. By slowing the sinus node firing, it helps relieve chest pain during exertion and supports better cardiac function in heart‑failure patients.

Ivabradine selectively blocks the HCN channels responsible for the funny (If) current in the sinoatrial node. This inhibition slows the spontaneous depolarisation of pacemaker cells, producing a controlled reduction in heart rate without affecting contractility or blood pressure, which improves myocardial oxygen balance.

The dose of Ivacorlan is individualized by the prescribing clinician based on the patient’s heart‑rate, clinical condition, and response to therapy. The prescriber determines the appropriate strength, frequency, and any necessary titration steps.

Safety data for ivabradine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Ivacorlan, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements), and necessary import documentation.

Both ivabradine and beta‑blockers lower heart rate, but ivabradine does so by selectively inhibiting the If current without affecting beta‑adrenergic receptors, myocardial contractility, or blood pressure. This makes ivabradine useful when beta‑blockers are contraindicated, not tolerated, or when additional heart‑rate reduction is needed.

Store Ivacorlan below 25 °C in its original packaging. Keep the product away from moisture, direct sunlight, and heat sources to maintain stability and potency throughout its shelf life.

Ivacorlan is taken orally, usually with a glass of water. The tablet should be swallowed whole and not chewed or crushed. Administration timing (e.g., with or without food) follows the prescriber’s instructions.

Serious adverse events include severe bradycardia, symptomatic atrial fibrillation, high‑grade atrioventricular block, and marked hypotension. Patients should report any fainting, dizziness, palpitations, or visual changes promptly to their healthcare provider.

Ivacorlan is contraindicated in patients with a resting heart rate below 60 bpm, severe hepatic impairment, sick‑sinus syndrome, second‑ or third‑degree AV block without a pacemaker, and in individuals taking strong CYP3A4 inhibitors unless dose adjustments are made.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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