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

Ivabradină Teva

Active Ingredient:
Ivabradine
Origin:
EU

Ivabradină Teva (Ivabradine)

Ivabradine, the active ingredient in Ivabradină 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 Ivabradină Teva as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Pharmaceuticals S.R.L

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Indications & Clinical Uses

Ivabradină Teva acts on the cardiac If current to lower heart rate in conditions where rate control improves outcomes.

  • Chronic stable angina pectoris: reduces the frequency of angina attacks and improves exercise tolerance.
  • Heart failure with reduced ejection fraction: lowers heart rate, alleviating symptoms and supporting cardiac function.
  • Chronic stable angina despite optimal therapy: provides additional symptom relief when beta‑blockers are insufficient.

How It Works

  • Ivabradine selectively blocks the funny (If) current in the sinoatrial node, which slows the spontaneous depolarisation of pacemaker cells. This results in a reduction of resting heart rate without decreasing myocardial contractility or blood pressure, helping to improve myocardial oxygen balance in angina and to lessen cardiac workload in heart failure.

Side Effects

Adverse reactions reported with Ivabradină Teva are generally related to its heart‑rate lowering action and visual perception.

Common Side Effects

  • Phosphenes (transient luminous phenomena)
  • Bradycardia
  • Headache
  • Dizziness
  • Fatigue
  • Visual blur

Serious or Rare Side Effects

  • Severe symptomatic bradycardia requiring medical intervention
  • Atrial fibrillation or other arrhythmias
  • Symptomatic hypotension
  • Persistent visual impairment
  • Allergic reactions including rash or angioedema

Precautions & Warnings

Before initiating therapy, clinicians should evaluate cardiovascular status and potential risk factors.

  • Cardiac assessment: confirm stable hemodynamics and absence of severe conduction disorders.
  • Conduction disease: avoid in patients with sick sinus syndrome or high-degree AV block unless a pacemaker is present.
  • Hepatic impairment: use with caution in moderate to severe liver disease.
  • Pregnancy and lactation: safety not established; weigh benefits against potential risks.
  • Pediatric use: not recommended as efficacy and safety have not been established in children.
  • Drug interactions: review concomitant medications that affect CYP3A4 or heart rate.
  • Store at ambient temperature: keep below 25°C in the original packaging, protect from moisture and light.

Avoid Interactions

Ivabradină Teva may interact with drugs that influence heart rate or its metabolic pathway.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase ivabradine plasma levels.
  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effect.
  • Concomitant use with other potent bradycardic agents (e.g., high‑dose beta‑blockers) can cause excessive heart‑rate reduction.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., diltiazem, verapamil): may require dose adjustment.
  • Other rate‑controlling drugs (e.g., digoxin, amiodarone): monitor heart rate and rhythm.
  • QT‑prolonging agents: observe for additive electrophysiological effects.

Frequently Asked Questions

Ivabradină Teva is prescribed for chronic stable angina pectoris and for heart failure with reduced ejection fraction. In both cases the drug helps lower heart rate, which reduces myocardial oxygen demand and improves symptoms.

Ivabradine selectively inhibits the funny (If) current in the sinoatrial node. By blocking this pacemaker current, the drug slows the spontaneous depolarisation of heart‑beat cells, producing a controlled reduction in resting heart rate without affecting contractility.

The dose of Ivabradină Teva is determined by the prescribing clinician based on the patient’s clinical condition, heart‑rate targets, and tolerability. The prescriber will adjust the regimen according to therapeutic response and safety monitoring.

Safety of ivabradine in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Ivabradină Teva, 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 blocking the If current without affecting beta‑adrenergic receptors, blood pressure, or myocardial contractility. This makes it useful when beta‑blockers are contraindicated, not tolerated, or insufficient alone.

Store Ivabradină Teva tablets at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct light, and ensure the container is tightly closed.

Ivabradină Teva is taken orally, usually with a glass of water. The tablet should be swallowed whole and not split, crushed, or chewed unless otherwise instructed by a healthcare professional.

Serious risks include severe bradycardia, atrial fibrillation, symptomatic hypotension, and rare visual disturbances that may be persistent. Patients should be monitored for these events, especially during dose initiation and adjustment.

Ivabradină Teva is contraindicated in patients with severe sinus node dysfunction, high‑grade atrioventricular block without a pacemaker, acute myocardial infarction, uncontrolled hypotension, and in individuals with known hypersensitivity to ivabradine or any excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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