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

Ivabradine Viatris

Active Ingredient:
Ivabradine Oxalate
Origin:
EU

Ivabradine Viatris (Ivabradine Oxalate)

Ivabradine, the active ingredient in Ivabradine Viatris, is a selective sinus node (If) channel inhibitor presented as an oral formulation for oral use. It reduces heart rate in patients with chronic stable angina and in those with heart failure with reduced ejection fraction, helping to improve symptoms and reduce cardiovascular events.

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

Manufacturer / TM Owner

Viatris Limited

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Indications & Clinical Uses

Ivabradine acts on the cardiac sinus node to lower heart rate, benefiting conditions where heart‑rate reduction improves outcomes.

  • Chronic stable angina pectoris: decreases the frequency of angina attacks by lowering myocardial oxygen demand.
  • Heart failure with reduced ejection fraction: improves symptoms and reduces hospitalization when added to standard heart‑failure therapy.

How It Works

  • Ivabradine selectively inhibits the funny (If) current in the sino‑atrial node, which controls spontaneous depolarization. By blocking this channel, the drug slows the pacemaker activity, leading to a reduction in heart rate without affecting myocardial contractility or systemic blood pressure, thereby decreasing cardiac workload.

Side Effects

Ivabradine may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Bradycardia: resting heart rate may fall below the desired range.
  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo: especially on standing.
  • Fatigue: general feeling of tiredness.

Serious or Rare Side Effects

  • Severe bradycardia requiring medical intervention.
  • Atrial fibrillation or other arrhythmias.
  • Symptomatic heart block.
  • Persistent visual disturbances affecting daily activities.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Monitor heart rate: ensure resting heart rate is above 60 bpm before starting.
  • Avoid in severe hepatic impairment: drug clearance may be reduced.
  • Caution in sick‑sinus syndrome: risk of excessive bradycardia.
  • Do not combine with strong CYP3A4 inhibitors: may increase plasma levels.
  • Store at ambient temperature (below 25°C): keep in the original pack, protect from moisture.

Avoid Interactions

Ivabradine can interact with other medicines, necessitating careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise ivabradine concentrations.
  • Other bradycardic agents (beta‑blockers, diltiazem, verapamil): risk of excessive heart‑rate reduction.
  • Certain anti‑arrhythmic drugs (e.g., amiodarone): can potentiate cardiac conduction effects.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole): may require dose adjustment.
  • Drugs affecting electrolyte balance (e.g., diuretics): monitor for arrhythmia risk.

Frequently Asked Questions

Ivabradine Viatris is prescribed to lower heart rate in patients with chronic stable angina pectoris and in those with heart failure with reduced ejection fraction, where heart‑rate reduction improves symptoms and clinical outcomes.

Ivabradine selectively blocks the funny (If) current in the sino‑atrial node, the pacemaker of the heart. This inhibition slows spontaneous depolarisation, reducing the heart‑rate without affecting contractility or blood pressure.

The dose of Ivabradine Viatris is individualized by the prescribing clinician based on the patient’s heart‑rate, clinical condition, and response to therapy. Specific dosing regimens are not provided here.

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 the treating physician.

To place an order, 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 and any necessary import documentation.

Both ivabradine and beta‑blockers lower heart rate, but ivabradine does so by selectively inhibiting the If current without affecting myocardial contractility or blood pressure, whereas beta‑blockers act on adrenergic receptors and can also reduce contractility and blood pressure.

Store Ivabradine Viatris at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture, and avoid exposure to direct sunlight.

Ivabradine Viatris is taken orally, usually with a glass of water. The tablet should be swallowed whole and not crushed or chewed, unless otherwise directed by a healthcare professional.

The most serious risks include severe bradycardia, atrial fibrillation, and symptomatic heart block. Patients should be monitored for signs of excessively low heart rate or arrhythmias, especially when combined with other heart‑rate‑lowering agents.

Ivabradine should be avoided in patients with severe hepatic impairment, sick‑sinus syndrome, or those taking strong CYP3A4 inhibitors. It is also contraindicated in individuals with a resting heart rate below 60 bpm unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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