Product image of Ivabradin Stada (Ivabradine Hydrochloride) supplied by GNH India

Ivabradin Stada

Active Ingredient:
Ivabradine Hydrochloride
Origin:
EU

Ivabradin Stada (Ivabradine Hydrochloride)

Ivabradine, the active ingredient in Ivabradin Stada, 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 certain forms of heart failure in adult patients.
GNH India supplies Ivabradin Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution.

Manufacturer / TM Owner

Stada Arzneimittel Gmbh

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Indications & Clinical Uses

Ivabradin Stada acts on the cardiac If current, making it useful in several heart‑related conditions.

  • Chronic stable angina: reduces frequency of angina attacks and improves exercise tolerance by lowering heart rate.
  • Heart failure with reduced ejection fraction: decreases hospitalization risk and enhances symptom control through heart‑rate reduction.
  • Ischemic heart disease: helps control myocardial oxygen demand by maintaining a lower heart rate.
  • Tachycardia associated with angina: provides rate control when beta‑blockers are insufficient or contraindicated.

How It Works

  • Ivabradine selectively blocks the funny (If) current in the sinoatrial node, slowing the spontaneous depolarisation of pacemaker cells. This results in a reduction of heart rate without affecting myocardial contractility, ventricular repolarisation, or systemic blood pressure, thereby decreasing cardiac oxygen demand.

Side Effects

Ivabradin Stada may cause a range of adverse reactions, which are categorized by frequency.

Common Side Effects

  • Visual disturbances (phosphenes): transient luminous phenomena, usually mild and reversible.
  • Bradycardia: heart‑rate reduction below 50 beats/min in some patients.
  • Headache: mild to moderate intensity, often transient.
  • Dizziness: sensation of light‑headedness, especially on standing.

Serious or Rare Side Effects

  • Symptomatic severe bradycardia: may cause fatigue, hypotension, or syncope.
  • Atrial fibrillation: irregular rapid heart rhythm requiring medical evaluation.
  • Persistent visual impairment: rare cases of lasting visual field changes.

Precautions & Warnings

Before prescribing Ivabradin Stada, clinicians should consider several safety precautions to minimize risk.

  • Cardiovascular assessment: evaluate baseline heart rate and conduction system.
  • Conduction disorders: avoid in patients with sick sinus syndrome or second‑degree AV block.
  • Severe hepatic impairment: use with caution or avoid as metabolism is reduced.
  • Pregnancy and lactation: safety not established; avoid unless benefit outweighs risk.
  • Drug interactions: review concomitant medications that affect CYP3A4 or heart rate.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Ivabradin Stada can interact with other medicines, influencing its plasma levels or additive heart‑rate effects.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): markedly increase ivabradine exposure.
  • Other bradycardic agents (beta‑blockers, digoxin, diltiazem): may cause excessive heart‑rate reduction.
  • Concomitant use with other If channel blockers: risk of profound bradycardia.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole, erythromycin): may raise levels, dose adjustment may be needed.
  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy.
  • Nitrates or other anti‑anginal drugs: monitor for additive effects on heart rate and blood pressure.

Frequently Asked Questions

Ivabradin Stada is an oral tablet containing ivabradine, indicated for chronic stable angina and for heart failure with reduced ejection fraction, where heart‑rate reduction improves symptoms and functional capacity.

Ivabradine selectively inhibits the funny (If) current in the sinoatrial node, slowing spontaneous depolarisation and thereby reducing heart rate without affecting myocardial contractility or blood pressure.

The dosage is individualized; a prescriber determines the appropriate strength and titration schedule based on the patient’s heart rate, clinical condition, and tolerability.

Safety data are limited; the product is classified as pregnancy category unknown, and it should be avoided unless the potential benefit justifies the potential risk to the fetus or infant.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams, verifies institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Both lower heart rate, but ivabradine acts selectively on the If channel without affecting myocardial contractility or blood pressure, making it useful when beta‑blockers are contraindicated or insufficient.

Store below 25 °C in the original packaging, protected from moisture and direct sunlight. Keep out of reach of children.

The tablet is taken orally with or without food, usually once daily at the same time each day, as directed by the prescribing clinician.

Serious adverse events include symptomatic severe bradycardia, atrial fibrillation, and rare persistent visual disturbances; patients should be monitored for these signs.

It is contraindicated in patients with severe hepatic impairment, sick sinus syndrome, second‑degree AV block, or resting heart rate below 50 beats/min, and should be avoided in pregnancy unless clearly needed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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