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 If channel inhibitor presented as a oral tablet for oral use. It treats chronic stable angina pectoris and heart failure with reduced ejection fraction in adult patients.

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 If current to lower heart rate, benefiting conditions where heart‑rate reduction improves outcomes.

  • Chronic stable angina pectoris: reduces the frequency of angina attacks by decreasing myocardial oxygen demand.
  • Heart failure with reduced ejection fraction (NYHA class II–III): improves exercise capacity and may lower hospitalization risk.
  • Elevated resting heart rate despite optimal therapy: provides additional heart‑rate control when beta‑blockers alone are insufficient.

How It Works

  • Ivabradine selectively inhibits the funny (If) current in the sino‑atrial node, which slows the spontaneous depolarization of pacemaker cells. This reduction in pacemaker activity lowers heart rate without affecting myocardial contractility or blood pressure, thereby decreasing cardiac oxygen consumption while preserving cardiac output.

Side Effects

Ivabradine may cause a range of adverse reactions, most of which are related to its heart‑rate‑lowering action or visual perception.

Common Side Effects

  • Bradycardia: heart rate falls below the intended therapeutic range.
  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness.
  • Fatigue or general weakness.

Serious or Rare Side Effects

  • Symptomatic bradycardia requiring medical intervention.
  • Atrial fibrillation or other significant arrhythmias.
  • Severe hypotension leading to syncope.
  • Persistent visual impairment or retinal disturbances.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential risks.

  • Cardiac monitoring: assess heart rate and rhythm regularly.
  • Contraindicated in severe hepatic impairment: avoid use due to altered metabolism.
  • Caution in sick‑sinus syndrome or atrioventricular block: may exacerbate conduction abnormalities.
  • Use with beta‑blockers only under supervision: risk of excessive bradycardia.
  • Pregnancy and lactation: safety not established; avoid unless clearly needed.
  • Store at below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Ivabradine can interact with several medicines that affect heart rate or its metabolism.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase ivabradine plasma levels.
  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy.
  • Concomitant bradycardic agents (e.g., beta‑blockers, digoxin) without dose adjustment: risk of severe bradycardia.

Moderate Interactions (Monitor Closely)

  • Calcium‑channel blockers diltiazem or verapamil: may modestly raise ivabradine concentrations.
  • Macrolide antibiotics (e.g., erythromycin, clarithromycin): potential increase in exposure.
  • Antidepressants affecting CYP3A4 (e.g., fluvoxamine): monitor heart rate and adjust if needed.

Frequently Asked Questions

Ivabradine Viatris is prescribed to manage chronic stable angina pectoris and heart failure with reduced ejection fraction (NYHA class II–III). It helps lower heart rate, reducing myocardial oxygen demand and improving exercise tolerance in these adult patients.

Ivabradine selectively blocks the funny (If) current in the sino‑atrial node, the pacemaker of the heart. By inhibiting this current, the drug slows the spontaneous depolarisation of pacemaker cells, resulting in a reduced heart rate without compromising contractile strength.

The dosage of Ivabradine Viatris is determined by the prescribing clinician based on the individual’s clinical condition, heart‑rate target, and tolerance. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety of ivabradine in pregnancy and lactation has not been established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and only under close medical supervision.

To request Ivabradine Viatris, 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. Beta‑blockers act on adrenergic receptors and have broader cardiovascular effects, which may be advantageous or limiting depending on the patient’s overall condition.

Ivabradine Viatris tablets should be stored at temperatures below 25 °C, in the original packaging, protected from moisture and direct light. Do not store in a refrigerator or freezer.

Ivabradine Viatris is taken orally as a tablet, usually with or without food as directed by the prescriber. The tablet should be swallowed whole with water and not crushed or chewed.

The most serious risks include symptomatic bradycardia, atrial fibrillation, severe hypotension, and rare visual disturbances that may be persistent. Patients should be monitored for these events, especially when initiating therapy or adjusting doses.

Ivabradine is contraindicated in patients with severe hepatic impairment, sick‑sinus syndrome, second‑ or third‑degree atrioventricular block, or those with a resting heart rate below 50 bpm. It should also be avoided in individuals with known hypersensitivity to ivabradine or any of its excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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