Product image of Ivabradina Farmoz (Ivabradine Hydrochloride) supplied by GNH India

Ivabradina Farmoz

Active Ingredient:
Ivabradine Hydrochloride
Origin:
EU

Ivabradina Farmoz (Ivabradine Hydrochloride)

Ivabradine, the active ingredient in Ivabradina Farmoz, is a If‑channel inhibitor presented as an oral dosage form for oral use. It reduces heart rate and is indicated for chronic stable angina and heart failure with reduced ejection fraction in adult patients with symptomatic disease.

GNH India supplies Ivabradina Farmoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support import and distribution across multiple regions.

Manufacturer / TM Owner

Farmoz - Sociedade Técnico Medicinal, S.A.

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Indications & Clinical Uses

  • Ivabradine acts on the cardiac If‑channel to lower heart rate, providing therapeutic benefit in angina and heart failure.
  • Chronic stable angina: decreases frequency of angina attacks and improves exercise tolerance.
  • Heart failure with reduced ejection fraction: lowers heart rate, which can improve symptoms and reduce hospitalization risk.
  • Ischemic heart disease (symptomatic): helps control heart rate and relieve chest discomfort.

How It Works

  • Ivabradine selectively binds to the funny (If) channels in the sinoatrial node, inhibiting the inward mixed Na⁺/K⁺ current that drives spontaneous depolarization. By reducing this pacemaker current, the drug slows the sinus rate without affecting myocardial contractility, ventricular repolarization, or blood pressure, resulting in a heart‑rate‑lowering effect that improves myocardial oxygen balance.

Side Effects

Ivabradina Farmoz may be associated with several adverse reactions, which are categorized by frequency and clinical significance.

Common Side Effects

  • Visual disturbances (phosphenes): transient luminous phenomena often reported as bright spots.
  • Bradycardia: heart rate falls below the prescribed range, potentially causing fatigue.
  • Headache: mild to moderate intensity, commonly occurring early in therapy.
  • Dizziness: sensation of light‑headedness, especially when standing quickly.

Serious or Rare Side Effects

  • Severe bradycardia leading to syncope or fainting episodes.
  • Atrial fibrillation: irregular rapid heart rhythm requiring medical attention.
  • Symptomatic hypotension: marked drop in blood pressure causing weakness.
  • Visual impairment (retinal): rare cases of blurred vision or visual field changes.

Precautions & Warnings

Before prescribing Ivabradina Farmoz, clinicians should consider several safety measures.

  • Cardiovascular assessment: evaluate baseline heart rate and rhythm before initiating therapy.
  • Monitor heart rate: regularly check pulse to ensure it remains above the recommended minimum.
  • Concomitant bradycardic agents: avoid or adjust dose when used with beta‑blockers, digoxin, or non‑dihydropyridine calcium‑channel blockers.
  • Hepatic impairment: use with caution in patients with moderate to severe liver dysfunction.
  • CYP3A4 inhibitors: avoid strong inhibitors such as ketoconazole or clarithromycin.
  • Store at ambient temperature: keep below 25 °C in original packaging, protect from moisture and light.

Avoid Interactions

Ivabradina Farmoz can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase ivabradine plasma levels and cause excessive bradycardia.
  • Co‑administration with other heart‑rate‑lowering drugs (beta‑blockers, digoxin, non‑dihydropyridine calcium‑channel blockers): risk of severe bradycardia and atrioventricular block.
  • Quinidine: can potentiate ivabradine effects and lead to marked heart‑rate reduction.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (diltiazem, verapamil): may require dose adjustment and close monitoring of heart rate.
  • CYP3A4 inducers (rifampicin, carbamazepine, phenytoin): may reduce ivabradine exposure and diminish efficacy.
  • Diuretics causing electrolyte imbalance: monitor electrolytes as shifts may affect cardiac conduction.

Frequently Asked Questions

Ivabradina Farmoz contains ivabradine, which is indicated for the treatment of chronic stable angina and for heart failure with reduced ejection fraction. In both conditions the drug lowers heart rate, helping to reduce chest pain episodes and improve cardiac efficiency.

Ivabradine works by selectively inhibiting the funny (If) current in the sinoatrial node. This reduces the spontaneous depolarisation that drives the heart’s pacemaker activity, slowing the sinus rhythm without affecting myocardial contractility or blood pressure.

The dose of Ivabradina Farmoz is determined by the prescribing clinician based on the patient’s clinical condition, heart‑rate response, and tolerability. Specific dosing regimens are not provided here and should follow the prescriber’s instructions and local labeling.

Safety data for ivabradine in pregnancy and lactation are limited. The product 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 health‑care professional.

To request Ivabradina Farmoz, 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 they act via different mechanisms. Ivabradine selectively blocks the If‑channel without affecting contractility or blood pressure, whereas beta‑blockers reduce heart rate by antagonising beta‑adrenergic receptors and also lower blood pressure. Choice of therapy depends on patient profile and tolerance.

Store Ivabradina Farmoz 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 to maintain stability.

Ivabradina Farmoz is taken orally. The tablet should be swallowed whole with a glass of water, preferably in the morning and evening, as directed by the prescriber. Food does not significantly affect its absorption, but patients should follow any specific timing instructions given by their clinician.

The most serious adverse reactions include severe bradycardia that can lead to syncope, atrial fibrillation, and symptomatic hypotension. Patients should be advised to report any episodes of fainting, rapid irregular heartbeats, or marked dizziness promptly to their health‑care provider.

Ivabradina Farmoz should be avoided in patients with a resting heart rate below 50 beats per minute, those with sick‑sinus syndrome, severe hepatic impairment, or in individuals taking strong CYP3A4 inhibitors that could raise ivabradine levels. Contra‑indications are detailed in the product label and should be reviewed by the prescriber.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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