Product image of Levosimendán Altan (Levosimendan) supplied by GNH India

Levosimendán Altan

Active Ingredient:
Levosimendan
Origin:
EU

Levosimendán Altan (Levosimendan)

Levosimendan, the active ingredient in Levosimendán Altan, is a calcium sensitizer presented as an intravenous solution for intravenous administration. It is indicated for the treatment of acute decompensated heart failure, providing inotropic support and vasodilation in hospitalized patients with severe cardiac dysfunction.

GNH India supplies Levosimendán Altan as a licensed, Good Distribution Practice‑compliant international pharmaceutical supplier, delivering the product to hospitals, transplant centres and specialty clinics worldwide while ensuring consistent quality and regulatory compliance.

Manufacturer / TM Owner

Altan Pharma Ltd

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Indications & Clinical Uses

Levosimendan is used in the management of acute decompensated heart failure, a condition characterized by sudden worsening of cardiac function.

  • Acute decompensated heart failure: improves cardiac output, reduces pulmonary congestion, and alleviates symptoms of low cardiac output in hospitalized patients.

How It Works

  • Levosimendan binds to cardiac troponin C, increasing its sensitivity to calcium, which enhances myocardial contractility without raising intracellular calcium levels. Simultaneously, it opens ATP‑sensitive potassium channels in vascular smooth muscle, causing arterial and venous vasodilation, thereby reducing cardiac preload and afterload and improving overall cardiac performance.

Side Effects

Levosimendan may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Hypotension: drop in blood pressure, especially after infusion start.
  • Headache: mild to moderate intensity.
  • Nausea: occasional gastrointestinal upset.
  • Dizziness: feeling light‑headed or unsteady.
  • Tachycardia: increased heart rate.
  • Flushing: warm sensation and reddening of skin.

Serious or Rare Side Effects

  • Severe hypotension: potentially requiring vasopressor support.
  • Ventricular arrhythmias: life‑threatening heart rhythm disturbances.
  • Myocardial ischemia: chest pain due to reduced coronary perfusion.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Pulmonary edema worsening: fluid accumulation in lungs.
  • Liver enzyme elevation: abnormal hepatic function tests.

Precautions & Warnings

Levosimendan requires careful clinical monitoring and specific handling precautions.

  • Blood pressure monitoring: observe for hypotension during and after infusion.
  • Cardiac rhythm surveillance: watch for arrhythmias, especially in patients with existing conduction disorders.
  • Renal function assessment: adjust use in severe renal impairment.
  • Hepatic function assessment: caution in patients with significant liver disease.
  • Concomitant vasodilator use: avoid simultaneous high‑dose nitrates or other vasodilators.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levosimendan can interact with several drug classes, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase levosimendan exposure.
  • Other calcium sensitizers: additive inotropic effect can cause excessive cardiac stimulation.
  • Potent vasodilators (e.g., high‑dose nitroglycerin): risk of severe hypotension.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate hypotensive effects.
  • Beta‑blockers: may blunt desired inotropic response.
  • ACE inhibitors or ARBs: monitor blood pressure and renal function.
  • Nitrates at standard doses: watch for additive vasodilation.
  • Other inotropes (e.g., dobutamine): assess for synergistic cardiac effects.

Frequently Asked Questions

Levosimendán Altan contains levosimendan, an intravenous calcium sensitizer indicated for the treatment of acute decompensated heart failure in hospitalized patients. It helps improve cardiac output and reduces symptoms associated with severe cardiac dysfunction.

Levosimendan increases the sensitivity of cardiac troponin C to calcium, enhancing contractility without raising intracellular calcium. It also opens ATP‑sensitive potassium channels in vascular smooth muscle, producing vasodilation that lowers preload and afterload, thereby supporting overall heart performance.

The dosing regimen for Levosimendán Altan is determined by the prescribing clinician based on the patient’s clinical condition, severity of heart failure, and response to therapy. The prescriber sets the infusion rate and duration according to approved guidelines.

Safety data for levosimendan during pregnancy and lactation are limited, and the product is generally not recommended for use in pregnant or breastfeeding women unless the potential benefit justifies the potential risk. Consultation with a specialist is essential.

To order Levosimendán Altan, 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 (including any cold‑chain requirements), and necessary import documentation.

Unlike traditional catecholamine inotropes, levosimendan enhances contractility by sensitizing troponin C to calcium and causes vasodilation via potassium‑channel opening. This dual action can improve cardiac output with a lower risk of increasing intracellular calcium‑related toxicity, offering a distinct therapeutic profile compared with agents such as dobutamine or dopamine.

Levosimendán Altan should be stored at 2‑8 °C, protected from light, and kept in its original packaging. Do not freeze or shake the solution. Before use, allow the product to reach room temperature if required by the administration protocol.

Levosimendán Altan is administered as an intravenous infusion. The infusion is typically started with a loading dose followed by a continuous maintenance infusion, as directed by the treating physician and according to institutional protocols.

Serious risks include severe hypotension, ventricular arrhythmias, myocardial ischemia, and rare allergic reactions. Patients should be closely monitored for blood pressure, heart rhythm, and signs of ischemia throughout the infusion and for a period after completion.

Levosimendán Altan is contraindicated in patients with known hypersensitivity to levosimendan or any excipients, those with severe hypotension (systolic blood pressure <90 mmHg), and individuals with significant obstructive cardiomyopathy where increased contractility could be harmful.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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