Product image of Ivabradine Krka (Ivabradine) supplied by GNH India

Ivabradine Krka

Active Ingredient:
Ivabradine
Origin:
EU

Ivabradine Krka (Ivabradine)

Ivabradine, the active ingredient in Ivabradine Krka, is a If channel inhibitor presented as an oral tablet for oral use. It reduces heart rate and is used to manage chronic stable angina and heart failure in adult patients.

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

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

  • Ivabradine acts on the cardiac If current to control heart rate in conditions where rate reduction improves outcomes.
  • Chronic stable angina: improves exercise tolerance and reduces the frequency of angina attacks.
  • Heart failure (NYHA class II‑III): lowers heart rate, alleviates symptoms and may decrease hospitalisations.
  • Ischemic heart disease: helps control heart rate when beta‑blockers are insufficient or not tolerated.

How It Works

  • Ivabradine selectively inhibits the funny (If) current in the sinoatrial node, which slows depolarisation of pacemaker cells. By reducing the slope of phase 4 depolarisation, it lowers heart rate without affecting myocardial contractility, ventricular repolarisation, or systemic vascular resistance.

Side Effects

Ivabradine may cause a range of adverse reactions, most of which are mild to moderate in severity.

Common Side Effects

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

Serious or Rare Side Effects

  • Symptomatic bradycardia requiring medical intervention.
  • Atrial fibrillation or other significant arrhythmias.
  • Severe hypotension leading to syncope.
  • High‑grade atrioventricular block.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient suitability and monitor for specific risks.

  • Heart rate monitoring: ensure resting heart rate remains above 50 bpm.
  • Hepatic impairment: use with caution in moderate to severe liver disease.
  • Concomitant bradycardic agents: avoid excessive heart‑rate reduction when combined with beta‑blockers or digoxin.
  • Sick sinus syndrome or atrioventricular block: contraindicated unless a pacemaker is present.
  • Pregnancy and lactation: safety not established; avoid unless benefits outweigh risks.
  • Store at room temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Ivabradine can interact with several drug classes, influencing heart rate or plasma concentrations.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase ivabradine levels.
  • Co‑administration with other bradycardic agents (beta‑blockers, digoxin): risk of excessive heart‑rate reduction.
  • Other If‑channel inhibitors: additive effect on pacemaker activity.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy.
  • Antihypertensive drugs: potential additive blood‑pressure lowering.
  • QT‑prolonging agents: may increase arrhythmia risk, requiring ECG monitoring.

Frequently Asked Questions

Ivabradine Krka is prescribed to lower heart rate in adults with chronic stable angina and in patients with heart failure classified as NYHA class II to III. By reducing the heart rate, it helps relieve angina symptoms and improves functional capacity in heart‑failure patients.

Ivabradine selectively blocks the funny (If) current in the sinoatrial node, which slows the spontaneous depolarisation of pacemaker cells. This action reduces the heart’s intrinsic rate without affecting contractility, allowing a controlled decrease in heart rate that improves myocardial oxygen balance.

The appropriate dose of Ivabradine Krka is determined by the prescribing clinician based on the patient’s clinical condition, heart‑rate response, and tolerability. Dosage adjustments are made according to therapeutic goals and any observed side effects.

Safety of ivabradine in pregnancy and lactation has not been established. 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. It is often used when beta‑blockers are contraindicated, not tolerated, or when additional heart‑rate reduction is needed.

Ivabradine Krka tablets should be stored at room temperature, below 25 °C. Keep them in the original packaging, protect from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Ivabradine Krka is taken orally, usually with or without food, as directed by the prescriber. The tablet should be swallowed whole with a glass of water and not chewed or crushed to preserve its intended release profile.

The most serious risks include symptomatic bradycardia, atrial fibrillation, severe hypotension, and high‑grade atrioventricular block. Patients should be monitored for these events, especially during dose initiation or when combined with other heart‑rate‑lowering agents.

Ivabradine is contraindicated in patients with severe hepatic impairment, sick sinus syndrome, second‑ or third‑degree atrioventricular block (unless a pacemaker is present), and in those with a resting heart rate below 50 bpm. It should also be avoided in patients taking strong CYP3A4 inhibitors without dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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