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

Ivabradine Grindeks

Active Ingredient:
Ivabradine Hydrochloride
Origin:
EU

Ivabradine Grindeks (Ivabradine Hydrochloride)

Ivabradine, the active ingredient in Ivabradine Grindeks, is a If channel inhibitor presented as an oral dosage form for oral use. It lowers heart rate and is indicated for chronic stable angina pectoris and heart failure with reduced ejection fraction in appropriate patients.

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

Manufacturer / TM Owner

Grindeks

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Indications & Clinical Uses

Ivabradine is an If channel inhibitor used in cardiovascular conditions that require heart‑rate reduction.

  • Chronic stable angina pectoris: reduces the frequency of angina attacks by lowering heart rate.
  • Heart failure with reduced ejection fraction (in combination with beta‑blockers): improves symptoms and lowers the risk of hospitalization.
  • Patients intolerant to beta‑blockers: provides heart‑rate control without affecting myocardial contractility.

How It Works

  • Ivabradine selectively binds to the funny (If) current channels in the sino‑atrial node, inhibiting the inward sodium/potassium mixed current that drives spontaneous depolarisation. This action slows the pacemaker activity, producing a dose‑dependent reduction in heart rate while preserving myocardial contractility and blood pressure.

Side Effects

Ivabradine may cause a range of adverse reactions, most of which are mild to moderate.

Common Side Effects

  • Bradycardia: heart rate falls below the desired range.
  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Headache.
  • Dizziness.
  • Fatigue.
  • Blurred vision.

Serious or Rare Side Effects

  • Symptomatic bradycardia requiring medical intervention.
  • Atrial fibrillation or other supraventricular arrhythmias.
  • Severe visual disturbances or persistent photopsia.
  • Hypotension leading to syncope.
  • Severe allergic reactions (e.g., rash, angioedema).
  • Conduction abnormalities such as heart block.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate cardiovascular status and monitor heart rate regularly.

  • Baseline heart rate assessment: ensure resting rate is above 70 bpm before starting.
  • Hepatic function: avoid or adjust dose in severe hepatic impairment.
  • Conduction disorders: contraindicated in sick sinus syndrome or advanced AV block.
  • Co‑administration with other bradycardic agents: use with caution when combined with beta‑blockers or digoxin.
  • CYP3A4 inhibitors: avoid strong inhibitors that may increase plasma levels.
  • Store at ambient temperature below 25 °C: keep in the original pack, protect from moisture.

Avoid Interactions

Ivabradine may interact with several medicines that affect heart rate or its metabolism.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise ivabradine concentrations.
  • Concomitant use with other potent heart‑rate‑lowering drugs (e.g., beta‑blockers, digoxin) when excessive bradycardia is a risk.
  • Drugs causing severe sinus node dysfunction.

Moderate Interactions (Monitor Closely):\n- Moderate CYP3A4 inhibitors (e.g., diltiazem, verapamil): may require dose adjustment.

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy.
  • Antihypertensive agents: monitor blood pressure for additive effects.

Frequently Asked Questions

Ivabradine Grindeks is prescribed to manage chronic stable angina pectoris and to treat heart failure with reduced ejection fraction, usually in combination with beta‑blockers. It helps relieve angina symptoms by lowering heart rate and improves functional capacity in selected heart‑failure patients.

Ivabradine works by selectively inhibiting the funny (If) current in the sino‑atrial node. This reduces the spontaneous depolarisation rate of pacemaker cells, leading to a controlled decrease in heart rate without compromising myocardial contractility or blood pressure.

The dosage of Ivabradine Grindeks is determined by the prescribing clinician based on the individual patient's heart‑rate, clinical condition, and tolerance. The prescriber will adjust the dose to achieve the target heart‑rate while monitoring for efficacy and safety.

Safety data for Ivabradine in pregnancy and lactation are limited. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and it is generally avoided unless no suitable alternatives exist.

To order Ivabradine Grindeks, 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 targeting the If current without affecting beta‑adrenergic receptors. Consequently, Ivabradine does not reduce myocardial contractility or blood pressure, making it useful when beta‑blockers are contraindicated or insufficient for heart‑rate control.

Ivabradine Grindeks should be stored at ambient temperature below 25 °C. Keep the tablets in the original container, protect them from moisture and direct sunlight, and ensure the packaging remains sealed until use.

Ivabradine Grindeks is taken orally, usually with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed to maintain its intended release profile.

The most serious risks include symptomatic bradycardia, atrial fibrillation, severe visual disturbances such as persistent photopsia, and conduction abnormalities like heart block. Patients should be monitored for these events, especially during dose initiation and titration.

Ivabradine Grindeks is contraindicated in patients with severe hepatic impairment, sick sinus syndrome, acute decompensated heart failure, unstable angina, or those with a resting heart rate below 70 bpm. Caution is also advised for individuals with existing conduction disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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