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

Ivabradine Teva

Active Ingredient:
Ivabradine
Origin:
EU

Ivabradine Teva (Ivabradine)

Ivabradine, the active ingredient in Ivabradine Teva, is an 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 rate control improves outcomes.

  • Chronic stable angina: reduces the frequency of angina attacks by lowering myocardial oxygen demand.
  • Heart failure with reduced ejection fraction: improves exercise capacity and lowers hospitalization risk through heart‑rate reduction.
  • Patients intolerant to beta‑blockers: provides a non‑beta‑blocker option for heart‑rate control in coronary disease.

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, the drug lowers heart rate without affecting myocardial contractility, ventricular repolarisation, or systemic blood pressure, thereby decreasing cardiac oxygen consumption.

Side Effects

Adverse reactions are reported across clinical use.

Common Side Effects

  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Bradycardia: heart rate below the intended therapeutic range.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo: often related to reduced heart rate.
  • Fatigue: general feeling of tiredness.
  • Blurred vision: occasional visual acuity changes.

Serious or Rare Side Effects

  • Severe bradycardia requiring medical intervention.
  • Atrial fibrillation or other arrhythmias.
  • Symptomatic hypotension.
  • Visual loss or persistent retinal disturbances.
  • Acute coronary syndrome in vulnerable patients.
  • Allergic reactions such as rash or angioedema.

Precautions & Warnings

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

  • Heart‑rate monitoring: ensure baseline rate is appropriate before dosing.
  • Hepatic impairment: use caution in moderate to severe liver disease.
  • Concomitant bradycardic agents: avoid combining with beta‑blockers or digoxin without supervision.
  • Sick‑sinus syndrome or atrioventricular block: contraindicated unless a pacemaker is present.
  • Pregnancy and lactation: safety not established; avoid unless benefits outweigh risks.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): can markedly increase plasma levels.
  • Other heart‑rate lowering agents (beta‑blockers, digoxin): risk of excessive bradycardia.
  • Drugs that prolong QT interval: additive risk of arrhythmia.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., diltiazem, verapamil): may require dose adjustment.
  • Antihypertensive agents: monitor blood pressure for additive effects.
  • CYP3A4 inducers (e.g., rifampicin): may reduce efficacy.
  • Herbal supplements affecting CYP enzymes: assess patient use.

Frequently Asked Questions

Ivabradine Teva is prescribed to manage chronic stable angina and heart failure with reduced ejection fraction. By selectively lowering heart rate, it helps reduce chest pain episodes in angina and improves functional capacity and reduces hospitalisations in patients with systolic heart failure.

Ivabradine blocks the funny (If) current in the sinoatrial node, which is responsible for spontaneous pacemaker activity. Inhibition slows the slope of phase‑4 depolarisation, decreasing the firing rate of the node and consequently lowering heart rate without affecting contractility or blood pressure.

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

Safety data for ivabradine in pregnancy and lactation are limited. It is generally advised to avoid use unless the potential benefit justifies the potential risk to the fetus or infant. Healthcare providers should discuss individual risk‑benefit considerations with the patient.

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 beta‑adrenergic receptors. This means it does not influence contractility or blood pressure, making it useful when beta‑blockers are contraindicated or not tolerated.

Ivabradine Teva tablets should be stored below 25 °C, in their original packaging, and protected from moisture and direct sunlight. Keeping the product in a dry, cool environment helps maintain its stability and potency throughout its shelf life.

Ivabradine Teva is taken orally, usually with a glass of water. It is commonly prescribed to be taken twice daily, with dosing times spaced 12 hours apart, but the exact schedule should follow the prescriber’s instructions.

The most serious risks include severe bradycardia, atrial fibrillation, symptomatic hypotension, and rare visual disturbances that may affect retinal function. Patients should be monitored for these events, especially during treatment initiation and dose adjustments.

Ivabradine Teva is contraindicated in patients with acute decompensated heart failure, severe hypotension, sick‑sinus syndrome, second‑ or third‑degree atrioventricular block (unless a pacemaker is present), 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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