Product image of Ivabradine Mercury Pharmaceuticals (Ivabradine) supplied by GNH India

Ivabradine Mercury Pharmaceuticals

Active Ingredient:
Ivabradine
Origin:
EU

Ivabradine Mercury Pharmaceuticals (Ivabradine)

Ivabradine, the active ingredient in Ivabradine Mercury Pharmaceuticals, is a selective If (funny) channel inhibitor presented as an oral dosage form for oral use. It is used to treat chronic heart failure and stable angina pectoris in adult patients. It is indicated for adult patients with reduced left ventricular ejection fraction and for those experiencing angina despite optimal therapy.

GNH India supplies Ivabradine Mercury Pharmaceuticals as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches to meet global demand.

Manufacturer / TM Owner

Mercury Pharmaceuticals Ltd.

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Indications & Clinical Uses

Ivabradine acts on cardiac rhythm disorders and angina by selectively inhibiting the If current in the sino‑atrial node.

  • Chronic heart failure: reduces heart rate, improving symptoms and exercise tolerance.
  • Stable angina pectoris: lowers heart rate, decreasing frequency of angina attacks.

How It Works

  • Ivabradine selectively binds to the pacemaker (If) channels in the sino‑atrial node, inhibiting the inward mixed sodium–potassium current that drives spontaneous depolarisation. By reducing this funny current, the drug slows the slope of phase 4 depolarisation, leading to a decrease in heart rate without affecting myocardial contractility or ventricular repolarisation.

Side Effects

Ivabradine may cause a range of adverse reactions, which are classified by frequency and severity.

Common Side Effects

  • Bradycardia: heart rate falls below the intended therapeutic range.
  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo: especially on standing.
  • Fatigue: generalised tiredness.
  • Blurred vision: temporary visual acuity changes.

Serious or Rare Side Effects

  • Symptomatic bradycardia requiring medical intervention.
  • Atrial fibrillation or other serious arrhythmias.
  • Severe hypotension leading to syncope.
  • Myocardial infarction in high‑risk patients.
  • Significant hepatic dysfunction.
  • Persistent visual impairment.

Precautions & Warnings

When prescribing ivabradine, clinicians should consider several precautionary measures to ensure patient safety.

  • Cardiovascular assessment: evaluate baseline heart rate and rhythm before initiation.
  • Concomitant bradycardic agents: monitor for excessive heart‑rate reduction when used with beta‑blockers or digoxin.
  • CYP3A4 inhibitors: avoid strong inhibitors or adjust dose as needed.
  • Pregnancy and lactation: safety not established; use only if benefit outweighs potential risk.
  • Hepatic or renal impairment: use with caution and consider dose adjustment.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Ivabradine can interact with other medicines, influencing its plasma concentration or additive cardiac effects.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may markedly increase ivabradine levels.
  • Other heart‑rate lowering agents (beta‑blockers, digoxin, diltiazem, verapamil): risk of profound bradycardia.
  • Concomitant use with other anti‑anginal drugs that affect conduction.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole, erythromycin): may require dose adjustment.
  • Antihypertensive agents: monitor blood pressure for additive effects.
  • Diuretics: watch for electrolyte disturbances that could affect cardiac rhythm.

Frequently Asked Questions

Ivabradine Mercury Pharmaceuticals is prescribed for adult patients with chronic heart failure and for those with stable angina pectoris. In both conditions it works by lowering the heart rate, which helps to reduce symptoms, improve exercise capacity, and decrease the frequency of angina attacks.

Ivabradine selectively blocks the funny (If) current in the sino‑atrial node, the heart’s natural pacemaker. By inhibiting this inward sodium‑potassium current, the drug slows the spontaneous depolarisation phase, resulting in a reduced heart‑rate without affecting the strength of cardiac contraction.

The dose of ivabradine is individualized by the prescribing clinician based on the patient’s heart‑rate, clinical condition, and response to therapy. The prescriber determines the appropriate strength, frequency, and any necessary titration, following local prescribing guidelines.

Safety data for ivabradine in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

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 required import documentation.

Both ivabradine and beta‑blockers lower heart rate, but ivabradine does so by directly inhibiting the If channel without affecting myocardial contractility or blood pressure. Beta‑blockers act on adrenergic receptors and have broader cardiovascular effects, which may be advantageous or limiting depending on the patient’s overall condition.

Ivabradine should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and direct sunlight. Maintaining these conditions helps preserve the tablet’s stability and potency throughout its shelf life.

Ivabradine is taken orally, usually with or without food, as directed by the prescriber. The tablets are swallowed whole with a glass of water and should be taken at the same times each day to maintain consistent blood levels.

The most serious risks include symptomatic bradycardia, atrial fibrillation, severe hypotension, and rare visual disturbances that may affect vision. Patients should be monitored for these events, especially when starting therapy or adjusting the dose.

Ivabradine is contraindicated in patients with severe hepatic impairment, acute decompensated heart failure, sick sinus syndrome, or a resting heart rate below 50 beats per minute. It should also be avoided in individuals taking strong CYP3A4 inhibitors unless dose adjustments are made under medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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