Product image of Ivabradine Uni-Pharma (Ivabradine) supplied by GNH India

Ivabradine Uni-Pharma

Active Ingredient:
Ivabradine
Origin:
EU

Ivabradine Uni-Pharma (Ivabradine)

Ivabradine, the active ingredient in Ivabradine Uni-Pharma, is a selective If (funny channel) inhibitor presented as an oral tablet for oral use. It reduces heart rate and is indicated for chronic stable angina pectoris and heart failure with reduced ejection fraction in appropriate patients.

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

Manufacturer / TM Owner

Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A.

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Indications & Clinical Uses

  • Ivabradine acts on the cardiac pacemaker If current, making it useful in conditions where heart‑rate reduction improves outcomes.
  • Chronic stable angina pectoris: improves exercise tolerance and decreases the frequency of angina episodes.
  • Heart failure with reduced ejection fraction (HFrEF): lowers resting heart rate, contributing to reduced hospitalisation risk.
  • Patients unsuitable for beta‑blockers: provides heart‑rate control when beta‑blockers are contraindicated or not tolerated.

How It Works

  • Ivabradine selectively binds to the hyperpolarisation‑activated cyclic nucleotide‑gated (HCN) channels that generate the If current in sino‑atrial node cells. By inhibiting this current, the drug slows spontaneous depolarisation, reducing heart rate without altering myocardial contractility or systemic blood pressure, thereby improving myocardial oxygen balance.

Side Effects

Adverse reactions are reported across a range of frequencies.

Common Side Effects

  • Bradycardia: heart rate falls below the intended therapeutic range.
  • Visual disturbances (phosphenes): transient luminous phenomena, especially in low‑light conditions.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo.
  • Fatigue or general weakness.
  • Blurred vision.

Serious or Rare Side Effects

  • Symptomatic severe bradycardia requiring medical intervention.
  • Atrial fibrillation or other significant arrhythmias.
  • High‑grade atrioventricular block.
  • Severe visual impairment or persistent photopsia.
  • Allergic reactions such as rash, pruritus or angio‑edema.
  • Hepatic dysfunction in susceptible individuals.

Precautions & Warnings

Careful assessment and monitoring are required before and during therapy.

  • Baseline heart rate: ensure resting rate is ≥60 bpm before initiation.
  • ECG monitoring: watch for excessive bradycardia or conduction abnormalities.
  • Severe hepatic impairment: avoid or use with extreme caution.
  • Sick sinus syndrome or AV‑block: contraindicated unless a pacemaker is present.
  • Renal impairment: dose adjustment may be needed.
  • Store at below 25°C: keep in the original pack, protect from moisture and light.

Avoid Interactions

Ivabradine may interact with several drug classes, altering its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase plasma levels.
  • Concomitant bradycardic agents (beta‑blockers, digoxin): risk of excessive heart‑rate reduction.
  • Drugs that affect AV‑node conduction (verapamil, diltiazem): may precipitate heart block.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (rifampicin, carbamazepine): may reduce therapeutic effect.
  • Diuretics causing electrolyte imbalance: can potentiate arrhythmic risk.
  • Other anti‑anginal agents (nitrates, ranolazine): monitor for additive haemodynamic effects.

Frequently Asked Questions

Ivabradine Uni-Pharma is prescribed to lower heart rate in patients with chronic stable angina pectoris and in those with heart failure with reduced ejection fraction (HFrEF). By slowing the heart, it helps relieve angina symptoms and can improve outcomes in heart‑failure patients when used alongside standard therapy.

Ivabradine selectively blocks the If (funny) current in the sino‑atrial node by binding to HCN channels. This inhibition slows the spontaneous depolarisation of pacemaker cells, leading to a reduction in heart rate without affecting the strength of cardiac contraction or blood pressure.

The dose of Ivabradine Uni-Pharma is determined by the prescribing clinician based on the patient’s clinical condition, baseline heart rate, and response to therapy. The prescriber will adjust the regimen to achieve the target heart‑rate range while monitoring safety.

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 must be made by the treating physician in consultation 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 myocardial contractility or blood pressure. Beta‑blockers act on adrenergic receptors and have broader haemodynamic effects, which may be advantageous or limiting depending on the patient’s comorbidities.

Ivabradine Uni-Pharma tablets should be stored at temperatures below 25 °C, in the original container, protected from moisture and direct sunlight. Keeping the product in a dry, cool place helps maintain its stability and potency throughout its shelf life.

The medication is taken orally, usually with or without food, as directed by the prescriber. Tablets should be swallowed whole with a glass of water and not chewed or crushed, unless otherwise instructed by a healthcare professional.

The most serious risks include symptomatic bradycardia, atrial fibrillation, high‑grade atrioventricular block, and severe visual disturbances such as persistent photopsia. Patients should be educated to report any episodes of dizziness, fainting, or visual changes promptly.

Ivabradine is contraindicated in patients with severe hepatic impairment, sick sinus syndrome, second‑ or third‑degree AV‑block without a pacemaker, and in those with a resting heart rate below 60 bpm. It should also be avoided in individuals taking strong CYP3A4 inhibitors unless dose adjustments are made.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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