Product image of Ivabradine Ingen Pharma (Ivabradine Oxalate) supplied by GNH India

Ivabradine Ingen Pharma

Active Ingredient:
Ivabradine Oxalate
Origin:
EU

Ivabradine Ingen Pharma (Ivabradine Oxalate)

Ivabradine, the active ingredient in Ivabradine Ingen Pharma, is an If channel inhibitor presented as an oral tablet for oral use. It lowers heart rate and is indicated for chronic stable angina and for patients with chronic heart failure who have an elevated resting heart rate.
GNH India supplies Ivabradine Ingen Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Sia Ingen Pharma

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Indications & Clinical Uses

Ivabradine acts on the cardiac If current to control heart rate in cardiovascular disease.

  • Chronic stable angina pectoris: reduces the frequency of angina attacks by lowering heart rate.
  • Chronic heart failure (reduced ejection fraction) with elevated heart rate: improves outcomes by decreasing myocardial oxygen demand.
  • Patients with coronary artery disease who cannot tolerate beta‑blockers: provides heart‑rate control as an alternative therapy.

How It Works

  • Ivabradine selectively inhibits the funny (If) current in the sino‑atrial node, which slows the spontaneous depolarisation of pacemaker cells. This reduction in the If current decreases heart rate without affecting myocardial contractility, ventricular repolarisation, or blood pressure, allowing a targeted heart‑rate lowering effect in patients with angina or heart failure.

Side Effects

Adverse reactions may occur with ivabradine therapy.

Common Side Effects

  • Bradycardia: resting heart rate may fall below expected levels.
  • Luminous phenomena (phosphenes): transient visual sensations of bright spots.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo: especially on standing.
  • Fatigue: general feeling of tiredness.
  • Blurred vision: temporary visual disturbances.

Serious or Rare Side Effects

  • Symptomatic bradycardia requiring medical intervention.
  • Atrial fibrillation or other serious arrhythmias.
  • Severe hypotension leading to syncope.
  • Allergic reactions such as rash, pruritus, or angioedema.
  • Visual disturbances persisting beyond transient phosphenes.

Precautions & Warnings

Before prescribing ivabradine, clinicians should consider several safety measures.

  • Assess baseline heart rate: ensure resting HR ≥ 60 bpm before initiation.
  • Monitor for bradycardia: discontinue if HR falls below 50 bpm or symptomatic.
  • Avoid in severe hepatic impairment: contraindicated due to altered metabolism.
  • Caution with concomitant CYP3A4 inhibitors: dose adjustment or avoidance may be required.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Ivabradine may interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase ivabradine plasma levels.
  • Co‑administration with other heart‑rate lowering agents (beta‑blockers, digoxin): risk of excessive bradycardia.
  • Verapamil (CYP3A4 inhibitor): may markedly raise ivabradine concentrations.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., diltiazem): may require dose adjustment.
  • Drugs that prolong the QT interval (e.g., certain antiarrhythmics): monitor ECG for additive effects.
  • Smoking: induces CYP3A4 and may reduce ivabradine efficacy.

Frequently Asked Questions

Ivabradine Ingen Pharma is used to lower heart rate in patients with chronic stable angina and in those with chronic heart failure with reduced ejection fraction who have an elevated resting heart rate. By reducing heart rate, it helps relieve angina symptoms and improves cardiac efficiency in heart‑failure patients.

Ivabradine selectively blocks the funny (If) current in the sino‑atrial node, the pacemaker of the heart. Inhibiting this current slows the spontaneous depolarisation of pacemaker cells, resulting in a reduced heart rate without affecting the strength of cardiac contraction or blood pressure.

The specific dose of ivabradine is determined by the prescribing clinician based on the patient’s clinical condition, baseline heart rate, and response to therapy. Dosage adjustments are made according to individual therapeutic goals and tolerability.

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 should be made by a qualified healthcare professional.

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. Beta‑blockers act on adrenergic receptors and have broader cardiovascular effects, making ivabradine a useful alternative when beta‑blockers are contraindicated or not tolerated.

Store the product at ambient temperature, preferably below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Ivabradine Ingen Pharma is taken orally, usually with or without food as directed by the prescribing physician. The tablets should be swallowed whole with a glass of water and not chewed or crushed.

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

Ivabradine should not be used in patients with a resting heart rate below 60 bpm, severe hepatic impairment, acute decompensated heart failure, sick sinus syndrome, or those taking strong CYP3A4 inhibitors without appropriate dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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