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

Levosimendan Altan

Active Ingredient:
Levosimendan
Origin:
EU

Levosimendan Altan (Levosimendan)

Levosimendan, the active ingredient in Levosimendan Altan, is a calcium sensitizer and K‑ATP channel opener presented as an intravenous solution for intravenous use. It treats acute decompensated heart failure and low‑output heart failure in adult patients.

GNH India supplies Levosimendan Altan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Altan Pharma Ltd

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Indications & Clinical Uses

  • Levosimendan is used in the management of heart‑failure conditions where enhanced cardiac contractility is required.
  • Acute decompensated heart failure: improves hemodynamics and reduces symptoms of congestion.
  • Low‑output heart failure: increases cardiac output and tissue perfusion.
  • Cardiogenic shock (off‑label): may provide hemodynamic support when conventional therapy is insufficient.

How It Works

  • Levosimendan binds to cardiac troponin C, increasing its sensitivity to calcium and thereby enhancing myocardial contractility without raising intracellular calcium levels. Simultaneously, it opens ATP‑dependent potassium channels in vascular smooth muscle, causing vasodilation and reducing after‑load, which together improve cardiac output in heart‑failure patients.

Side Effects

Levosimendan may cause a range of adverse reactions, from mild to severe. Monitoring and prompt management are essential.

Common Side Effects

  • Hypotension: drop in blood pressure, especially after loading dose.
  • Headache: mild to moderate intensity.
  • Nausea: occasional gastrointestinal upset.
  • Flushing: transient warmth and redness of skin.
  • Tachycardia: increased heart rate.

Serious or Rare Side Effects

  • Severe hypotension: may require vasopressor support.
  • Ventricular arrhythmias: potentially life‑threatening rhythm disturbances.
  • Myocardial ischemia: chest pain or ECG changes.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Liver enzyme elevation: abnormal hepatic function tests.

Precautions & Warnings

Levosimendan requires careful patient assessment and monitoring before and during infusion.

  • Blood pressure monitoring: check for hypotension before initiation and regularly during infusion.
  • Cardiac rhythm assessment: observe for arrhythmias, especially in patients with pre‑existing conduction disorders.
  • Dose adjustment: consider reduced dosing in severe renal or hepatic impairment.
  • Concomitant vasodilators: avoid or use with caution when combined with other potent vasodilators.
  • Pregnancy and lactation: safety not established; use only if benefit outweighs risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levosimendan can interact with several drug classes, influencing cardiovascular stability.

Major Interactions (Avoid)

  • Potent vasodilators (e.g., nitroglycerin): may cause profound hypotension.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): increase levosimendan exposure.
  • Other inotropes (e.g., dobutamine): risk of excessive cardiac stimulation.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may blunt desired inotropic effect.
  • Diuretics: monitor electrolyte balance and volume status.
  • ACE inhibitors/ARBs: watch for additive blood‑pressure lowering.
  • Calcium channel blockers: potential additive vasodilation.
  • Antiarrhythmic agents: observe for rhythm changes.

Frequently Asked Questions

Levosimendan Altan is indicated for the treatment of acute decompensated heart failure and low‑output heart failure in adult patients. It may also be used off‑label in cardiogenic shock when conventional therapies are insufficient, providing inotropic support and vasodilation.

Levosimendan enhances cardiac contractility by sensitising troponin C to calcium, allowing stronger heart muscle contractions without raising intracellular calcium. At the same time, it opens ATP‑dependent potassium channels in vascular smooth muscle, producing vasodilation and reducing cardiac after‑load.

The dosing regimen for Levosimendan Altan is determined by the prescribing clinician based on the patient’s clinical status, weight, and response. The prescriber sets the loading dose, infusion rate, and duration according to approved guidelines and individual needs.

Safety of levosimendan in pregnancy and lactation has not been established. It should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by the treating physician.

To order Levosimendan 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 cold‑chain where needed), and import documentation.

Unlike traditional catecholamine inotropes, levosimendan increases contractility without raising intracellular calcium, reducing the risk of calcium‑mediated toxicity. Its simultaneous vasodilatory effect can lower after‑load, whereas many other inotropes may increase myocardial oxygen demand and cause tachyarrhythmias.

Levosimendan Altan should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Keep the solution in its original packaging until use to maintain stability and sterility.

Levosimendan Altan is supplied as an intravenous solution. It is typically given as an initial loading infusion followed by a continuous maintenance infusion, administered by a healthcare professional in a monitored setting such as an intensive care or cardiac unit.

The most serious risks include severe hypotension, ventricular arrhythmias, myocardial ischemia, and rare allergic reactions. Continuous cardiovascular monitoring is essential during infusion to detect and manage these events promptly.

Levosimendan is contraindicated in patients with severe hypotension, uncontrolled ventricular arrhythmias, or known hypersensitivity to the drug or its excipients. Caution is also advised in individuals with significant renal or hepatic impairment, unless dose adjustments are made.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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