Product image of Ivabradina Eg (Ivabradine Hydrochloride) supplied by GNH India

Ivabradina Eg

Active Ingredient:
Ivabradine Hydrochloride
Origin:
EU

Ivabradina Eg (Ivabradine Hydrochloride)

Ivabradine, the active ingredient in Ivabradina Eg, is an If (funny) channel inhibitor presented as an oral tablet for oral use. It selectively inhibits the cardiac pacemaker If current in the sino‑atrial node, leading to heart‑rate reduction without affecting myocardial contractility. It is employed in the management of chronic stable angina pectoris and heart failure with reduced ejection fraction in adult patients.

GNH India supplies Ivabradina Eg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable sourcing for cardiovascular therapeutics across multiple continents.

Manufacturer / TM Owner

Eg S.P.A.

1
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Indications & Clinical Uses

Ivabradine is used to manage cardiovascular conditions where heart‑rate reduction improves outcomes.

  • Chronic stable angina pectoris: reduces frequency of angina attacks and improves exercise tolerance.
  • Heart failure with reduced ejection fraction: lowers heart rate, alleviating symptoms and supporting cardiac function.

How It Works

  • Ivabradine selectively binds to the hyperpolarization‑activated cyclic nucleotide‑gated (HCN) channels that generate the If current in sino‑atrial node pacemaker cells. By inhibiting this inward mixed Na⁺/K⁺ current, the drug slows spontaneous depolarization, decreasing the heart rate without compromising myocardial contractility or ventricular repolarisation. The effect is dose‑dependent and reversible, allowing heart‑rate control while preserving blood pressure and cardiac output. Ivabradine does not interact with beta‑adrenergic receptors, distinguishing it from beta‑blockers.

Side Effects

Ivabradine may be associated with several adverse reactions, ranging from frequent, mild events to rare, serious conditions.

Common Side Effects

  • Bradycardia: slower than intended heart rate.
  • Visual disturbances (phosphenes): transient luminous phenomena.
  • Headache: mild to moderate intensity.

Serious or Rare Side Effects

  • Symptomatic bradycardia: may cause syncope or hypotension.
  • Atrial fibrillation: irregular heart rhythm.
  • Allergic reactions: rash, pruritus, or anaphylaxis.

Precautions & Warnings

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

  • Cardiac monitoring: assess resting heart rate before initiation and periodically during therapy.
  • Concomitant beta‑blockers: avoid excessive heart‑rate lowering by adjusting doses.
  • Severe hepatic impairment: use with caution as metabolism may be reduced.
  • Pregnancy and lactation: contraindicated unless benefits outweigh potential risks.
  • Drug interactions: review concomitant medications that affect CYP3A4 metabolism.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Ivabradine can interact with other medicines, influencing its plasma concentration or combined physiological effects.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may markedly increase ivabradine levels.
  • Concomitant diltiazem or verapamil: can cause pronounced bradycardia.
  • Other heart‑rate lowering agents (beta‑blockers, digoxin): risk of excessive bradycardia.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., erythromycin): may require dose adjustment.
  • QT‑prolonging drugs: monitor ECG for interval changes.
  • Hypotensive agents: observe for additive blood pressure reduction.

Frequently Asked Questions

Ivabradina Eg contains ivabradine, which is prescribed to lower heart rate in adults with chronic stable angina pectoris and in patients with heart failure with reduced ejection fraction, helping to reduce angina episodes and improve heart‑failure symptoms.

Ivabradine selectively blocks the If (funny) current in the sino‑atrial node by binding to HCN channels. This slows the spontaneous depolarisation of pacemaker cells, reducing heart rate without affecting myocardial contractility or blood pressure.

The dose of ivabradine is individualized by the prescribing clinician based on the patient’s heart‑rate, clinical condition, and response to therapy. Dosage adjustments follow local prescribing guidelines and are not predetermined by the product label.

Ivabradine is generally contraindicated during pregnancy and lactation unless the potential benefit justifies the potential risk to the fetus or infant. Clinicians should evaluate the risk‑benefit profile before prescribing to pregnant or nursing women.

To request Ivabradina Eg, 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 acts specifically on the If channel and does not affect beta‑adrenergic receptors, so it does not influence blood pressure or contractility. This makes it a useful adjunct or alternative when beta‑blockers are contraindicated or insufficient.

Store Ivabradina Eg at ambient temperature, preferably below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct light, and ensure the container is tightly closed to maintain product stability.

Ivabradina Eg is taken orally, usually with a glass of water. The tablet should be swallowed whole and not crushed or chewed. Administration timing and frequency are determined by the prescribing healthcare professional.

Serious risks include symptomatic bradycardia that can lead to syncope, atrial fibrillation, and severe allergic reactions such as anaphylaxis. Patients should be monitored for these events, especially when the drug is combined with other heart‑rate‑lowering agents.

Ivabradine should be avoided in patients with severe hepatic impairment, uncontrolled hypotension, acute decompensated heart failure, or known hypersensitivity to the drug. It is also contraindicated in individuals with certain rhythm disorders, such as sick sinus syndrome, unless a pacemaker is in place.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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