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

Ivabradine Cf

Active Ingredient:
Ivabradine Hydrochloride
Origin:
EU

Ivabradine Cf (Ivabradine Hydrochloride)

Ivabradine, the active ingredient in Ivabradine Cf, is a If channel inhibitor presented as an oral formulation for oral use. It is used to manage chronic stable angina and heart failure with reduced ejection fraction in appropriate patients.

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

Manufacturer / TM Owner

Centrafarm B.V.

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Indications & Clinical Uses

Ivabradine acts on the cardiac If current to control heart rate, making it useful in several cardiovascular conditions.

  • Chronic stable angina: reduces the frequency of angina episodes and improves exercise tolerance.
  • Heart failure with reduced ejection fraction: lowers heart rate, which can improve functional capacity and decrease hospitalisations.
  • Symptomatic angina in patients intolerant to beta‑blockers: provides an alternative means of heart‑rate reduction.

How It Works

  • Ivabradine selectively inhibits the funny (If) current in the sinoatrial node, which slows spontaneous depolarisation. By reducing the pacemaker activity, the drug lowers heart rate without compromising myocardial contractility or blood pressure, thereby decreasing myocardial oxygen demand in patients with angina or heart failure.

Side Effects

Adverse reactions may occur with ivabradine therapy.

Common Side Effects

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

Serious or Rare Side Effects

  • Symptomatic severe bradycardia requiring medical attention.
  • Atrial fibrillation or other significant arrhythmias.
  • Severe hypotension leading to syncope.
  • High‑grade atrioventricular block.
  • Vision loss or persistent visual impairment.
  • Life‑threatening allergic reactions (anaphylaxis).

Precautions & Warnings

Before initiating ivabradine, clinicians should consider several safety aspects.

  • Cardiovascular assessment: evaluate baseline heart rate and rhythm.
  • Concomitant bradycardic agents: avoid or adjust dose when used with beta‑blockers, digoxin, or calcium‑channel blockers.
  • CYP3A4 inhibitors: avoid strong inhibitors that may increase ivabradine exposure.
  • Hepatic impairment: use with caution in moderate to severe liver disease.
  • Pregnancy and lactation: safety not established; avoid unless clearly needed.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Ivabradine may interact with other medicines, altering its effectiveness or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): can markedly increase plasma levels.
  • Other heart‑rate‑lowering drugs (beta‑blockers, digoxin, diltiazem): risk of excessive bradycardia.
  • AV‑nodal blocking agents: may precipitate atrioventricular block.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole): may require dose adjustment.
  • Antihypertensive agents: monitor blood pressure for additive effects.
  • Diuretics: watch for electrolyte disturbances that could affect cardiac conduction.
  • Other anti‑anginal medications: assess overall heart‑rate control.

Frequently Asked Questions

Ivabradine Cf is prescribed for chronic stable angina and for heart failure with reduced ejection fraction. In both conditions it works by lowering heart rate, which reduces myocardial oxygen demand and can improve symptoms and functional capacity.

Ivabradine selectively blocks the funny (If) current in the sinoatrial node, the heart’s natural pacemaker. By inhibiting this current, the drug slows the spontaneous depolarisation of pacemaker cells, resulting in a reduced heart rate without affecting contractile strength.

The appropriate dose of Ivabradine Cf is determined by the prescribing clinician based on the patient’s clinical status, heart‑rate targets, and any concomitant therapies. Dosage adjustments are made according to individual response and tolerability.

Safety data for ivabradine in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and under close medical supervision.

To request Ivabradine Cf, 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 without affecting myocardial contractility or blood pressure. It is often considered when patients cannot tolerate beta‑blockers or when additional heart‑rate reduction is needed beyond what beta‑blockers provide.

Ivabradine Cf should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original container, protect them from moisture, heat and direct sunlight to maintain product stability.

Ivabradine Cf is taken orally, usually with or without food as directed by the prescriber. The tablets should be swallowed whole with a glass of water and not crushed or chewed.

The most serious risks include symptomatic bradycardia, atrial fibrillation, high‑grade atrioventricular block, severe hypotension, and rare visual disturbances that may lead to vision loss. Patients should be monitored for these events, especially during treatment initiation and dose changes.

Ivabradine Cf is contraindicated in patients with severe hepatic impairment, acute decompensated heart failure, sick sinus syndrome, or those with a resting heart rate below 50 bpm. It should also be avoided in individuals taking strong CYP3A4 inhibitors or other potent bradycardic agents without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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