Product image of Ivabradine Teva (Ivabradine Hydrochloride) supplied by GNH India

Ivabradine Teva

Active Ingredient:
Ivabradine Hydrochloride
Origin:
EU

Ivabradine Teva (Ivabradine Hydrochloride)

Ivabradine, the active ingredient in Ivabradine Teva, is a If channel inhibitor presented as an oral tablet for oral use. It treats chronic stable angina and heart failure with reduced ejection fraction in adult patients.

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

Manufacturer / TM Owner

Teva B.V

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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: decreases the frequency of angina attacks by reducing myocardial oxygen demand.
  • Heart failure with reduced ejection fraction (HFrEF): improves exercise capacity and may lower hospitalization risk.
  • Inappropriate sinus tachycardia: provides rate control when beta‑blockers are unsuitable.

How It Works

  • Ivabradine selectively inhibits the funny (If) current in the sinoatrial node, which slows spontaneous depolarisation. By reducing the slope of phase 4 depolarisation, it lowers heart rate without affecting myocardial contractility or intracardiac conduction, thereby decreasing cardiac oxygen consumption while preserving systolic function.

Side Effects

Ivabradine is generally well tolerated, but several adverse reactions have been reported.

Common Side Effects

  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness.
  • Fatigue or general weakness.
  • Nausea or gastrointestinal discomfort.
  • Bradycardia (heart rate <50 bpm).

Serious or Rare Side Effects

  • Severe bradycardia requiring medical intervention.
  • Atrial fibrillation or other significant arrhythmias.
  • Symptomatic hypotension.
  • High‑grade atrioventricular block.
  • Persistent visual loss.
  • Allergic reactions such as rash or angioedema.

Precautions & Warnings

Before initiating ivabradine, clinicians should consider several safety aspects.

  • Cardiac monitoring: obtain baseline heart‑rate and ECG to ensure rate >60 bpm.
  • Concomitant bradycardic agents: avoid combining with beta‑blockers or digoxin without careful monitoring.
  • Severe hepatic impairment: use with caution as metabolism may be reduced.
  • Pregnancy: avoid unless the potential benefit justifies the risk to the fetus.
  • Renal impairment: assess renal function; dose adjustment may be needed.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Ivabradine may interact with several medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): increase ivabradine plasma concentrations.
  • Other bradycardic agents (e.g., beta‑blockers, digoxin): risk of severe bradycardia.
  • QT‑prolonging drugs (e.g., certain antiarrhythmics): heightened arrhythmia risk.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce ivabradine effectiveness.
  • Calcium‑channel blockers verapamil or diltiazem: can raise ivabradine levels.
  • Antacids containing aluminium or magnesium: may decrease oral absorption of ivabradine.

Frequently Asked Questions

Ivabradine Teva is prescribed to lower heart rate in patients with chronic stable angina and in those with heart failure with reduced ejection fraction, helping to reduce angina episodes and improve functional capacity.

Ivabradine selectively blocks the funny (If) current in the sinoatrial node, slowing the spontaneous depolarisation that initiates each heartbeat. This reduces heart rate without affecting the strength of cardiac contraction.

The dose of Ivabradine Teva is individualized by the prescribing clinician based on the patient’s heart‑rate, clinical condition, and tolerance. Dosage adjustments follow the prescriber’s assessment and local labeling.

Safety data for ivabradine in pregnancy and lactation are limited. It should be avoided unless the potential benefit outweighs the possible risk to the fetus or infant, and only under specialist guidance.

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 required import documentation.

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

Store Ivabradine Teva at ambient temperature, below 25 °C, in the original packaging. Keep the product away from moisture, direct sunlight and excessive heat to maintain stability.

Ivabradine Teva is taken orally, usually with a glass of water. It is typically administered twice daily, but the exact schedule is determined by the prescriber based on the patient’s clinical response.

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

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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