Product image of Ivabradina Sandoz (Ivabradine Oxalate) supplied by GNH India

Ivabradina Sandoz

Active Ingredient:
Ivabradine Oxalate
Origin:
EU

Ivabradina Sandoz (Ivabradine Oxalate)

Ivabradine, the active ingredient in Ivabradina Sandoz, is an If channel inhibitor presented as an oral tablet for oral use. It lowers heart rate and is indicated for chronic stable angina and heart failure in adult patients, helping to reduce angina episodes and improve functional capacity.

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

Manufacturer / TM Owner

Sandoz S.P.A.

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Indications & Clinical Uses

Ivabradina Sandoz acts on the cardiac If current to manage conditions where heart‑rate reduction is therapeutic.

  • Chronic stable angina: improves exercise tolerance and decreases frequency of angina attacks.
  • Heart failure with reduced ejection fraction: lowers resting heart rate and may enhance symptom control.
  • Elevated heart rate despite optimal therapy: provides additional rate control when beta‑blockers are insufficient or not tolerated.

How It Works

  • Ivabradine selectively inhibits the funny (If) current in sinoatrial node cells, which slows depolarisation of pacemaker cells. By reducing the slope of phase 4 depolarisation, the drug decreases spontaneous heart‑rate without affecting myocardial contractility, ventricular repolarisation, or blood pressure, thereby providing rate control in angina and heart‑failure patients.

Side Effects

Adverse reactions may occur with Ivabradina Sandoz and are reported in clinical use.

Common Side Effects

  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Bradycardia: heart rate below prescribed limits.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo: especially on standing.
  • Fatigue: general feeling of tiredness.
  • Nausea: occasional gastrointestinal upset.

Serious or Rare Side Effects

  • Symptomatic bradycardia requiring medical attention.
  • Atrial fibrillation or other arrhythmias.
  • Severe hypotension leading to syncope.
  • Persistent visual loss or retinal abnormalities.
  • Hepatic enzyme elevation indicating possible liver injury.

Precautions & Warnings

Before initiating Ivabradina Sandoz, clinicians should consider several safety measures.

  • Baseline heart rate: ensure resting rate is ≥60 bpm before starting therapy.
  • Concomitant bradycardic agents: evaluate need for dose adjustment or monitoring.
  • Severe hepatic impairment: use with caution or avoid.
  • Pregnancy and lactation: assess risk‑benefit, as safety data are limited.
  • Elderly patients: monitor for increased sensitivity to heart‑rate effects.
  • Store below 25°C: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Ivabradina Sandoz may interact with other medicines; awareness of interaction severity guides clinical decisions.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may markedly increase ivabradine exposure.
  • Co‑administration with other heart‑rate‑lowering drugs (beta‑blockers, digoxin, diltiazem): risk of excessive bradycardia.
  • Concomitant use with drugs that cause QT prolongation: may increase arrhythmic risk.

Moderate Interactions (Monitor Closely):\n- CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce ivabradine effectiveness.

  • Verapamil or diltiazem (moderate CYP3A4 inhibitors): may require dose adjustment.
  • Alcohol consumption: can enhance bradycardic effects and should be limited.

Frequently Asked Questions

Ivabradina Sandoz is prescribed to lower heart rate in adults with chronic stable angina and in patients with heart failure with reduced ejection fraction, helping to reduce angina episodes and improve functional capacity.

Ivabradine selectively blocks the funny (If) current in the sinoatrial node, slowing the spontaneous depolarisation of pacemaker cells. This reduces the heart’s intrinsic rate without affecting contractility or blood pressure.

The dose of Ivabradina Sandoz is determined by the prescribing clinician based on the patient’s clinical condition, heart‑rate response, and tolerability. Dosage adjustments are made according to therapeutic goals and safety monitoring.

Safety data for ivabradine in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies the potential 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 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. It may be used when beta‑blockers are contraindicated, not tolerated, or insufficient for heart‑rate control.

Ivabradina Sandoz should be stored below 25 °C in its original packaging, protected from moisture and direct sunlight. Do not store in a humid environment or expose the tablets to excessive heat.

Ivabradina Sandoz is taken orally, usually with water. The tablet should be swallowed whole and not split, crushed, or chewed unless otherwise directed by a healthcare professional.

Serious risks include symptomatic bradycardia, atrial fibrillation, severe hypotension, and rare visual disturbances that may lead to persistent vision loss. Patients should be monitored for these events, especially during dose initiation and titration.

Ivabradina Sandoz is contraindicated in patients with a resting heart rate below 60 bpm, those with severe hepatic impairment, and individuals with known hypersensitivity to ivabradine or any excipients in the formulation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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