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

Ivabradine Zydus

Active Ingredient:
Ivabradine Hydrochloride
Origin:
EU

Ivabradine Zydus (Ivabradine Hydrochloride)

Ivabradine, the active ingredient in Ivabradine Zydus, is a If channel inhibitor presented as an oral tablet for oral use. It lowers heart rate and is used to manage chronic stable angina and heart failure with reduced ejection fraction in adult patients.
GNH India supplies Ivabradine Zydus as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Zydus France

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Indications & Clinical Uses

Ivabradine acts on the cardiac If current to control heart rate in specific cardiovascular conditions.

  • Chronic stable angina pectoris: reduces the frequency of angina attacks by lowering heart rate without affecting contractility.
  • Heart failure with reduced ejection fraction (HFrEF): decreases heart rate to improve ventricular filling and functional capacity.
  • Symptomatic sinus tachycardia (off‑label in some regions): may be used to control elevated resting heart rate when other agents are unsuitable.

How It Works

  • Ivabradine selectively inhibits the funny (If) current in the sino‑atrial node, which is responsible for spontaneous depolarization during diastole. By blocking this inward sodium‑potassium mixed current, the drug slows the pacemaker activity, leading to a reduction in heart rate while preserving myocardial contractility and intracardiac conduction.

Side Effects

Ivabradine may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Bradycardia: heart rate slower than intended.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo.
  • Fatigue or general weakness.
  • Nausea or gastrointestinal discomfort.

Serious or Rare Side Effects

  • Symptomatic severe bradycardia requiring medical attention.
  • Atrial fibrillation or other arrhythmias.
  • Persistent visual impairment.
  • Severe hypotension.
  • Allergic reactions such as rash or angioedema.
  • Myocardial ischemia exacerbation.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient-specific factors and monitor for potential risks.

  • Cardiac monitoring: assess resting heart rate and ECG prior to starting treatment.
  • Concomitant beta‑blockers: avoid excessive bradycardia by adjusting doses.
  • CYP3A4 inhibitors: consider dose reduction or increased monitoring.
  • Renal impairment: use with caution and monitor renal function.
  • Pregnancy: safety not established; avoid unless benefit outweighs risk.
  • Store at below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Ivabradine can interact with several medicines, necessitating careful review of a patient’s regimen.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may markedly increase plasma concentrations.
  • Verapamil or diltiazem: combined use can cause excessive bradycardia.
  • Other potent heart‑rate lowering agents (high‑dose beta‑blockers): risk of severe bradycardia.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effect.
  • Drugs that prolong QT interval (certain antidepressants, antipsychotics): monitor ECG for arrhythmia risk.
  • Diuretics causing electrolyte shifts: watch for hypotension and electrolyte abnormalities.

Frequently Asked Questions

Ivabradine Zydus is prescribed to lower heart rate in adults with chronic stable angina pectoris and in patients with heart failure with reduced ejection fraction. By reducing the heart rate, it helps relieve angina symptoms and improves cardiac efficiency in heart failure.

Ivabradine selectively blocks the funny (If) current in the sino‑atrial node, the pacemaker of the heart. This inhibition slows the spontaneous depolarisation of the node, resulting in a lower heart rate while preserving myocardial contractility and normal conduction pathways.

The dosage of Ivabradine Zydus is individualized by the prescribing clinician based on the patient’s heart rate, clinical condition, and response to therapy. The prescriber determines the appropriate starting dose and any subsequent adjustments.

Safety data for Ivabradine Zydus in pregnancy and lactation are limited. It should be avoided unless the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com with 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 can also reduce contractility and blood pressure, making Ivabradine a useful alternative when those effects are undesirable.

Ivabradine Zydus tablets should be stored at temperatures below 25 °C, in the original packaging, and protected from moisture and direct sunlight. Keep the container tightly closed and out of reach of children.

The medication is taken orally as a whole tablet, usually with or without food. Patients should swallow the tablet whole with a glass of water and follow the dosing schedule prescribed by their healthcare provider.

The most serious adverse events include symptomatic severe bradycardia, atrial fibrillation, marked hypotension, and persistent visual disturbances. Patients should seek immediate medical attention if they experience fainting, rapid irregular heartbeats, or sudden vision changes.

Ivabradine Zydus is contraindicated in patients with severe hypotension, sick sinus syndrome, atrial fibrillation, or those using strong CYP3A4 inhibitors. It should also be avoided in individuals with known hypersensitivity to ivabradine or any of its excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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