Product image of Levatrop (Levosimendan) supplied by GNH India

Levatrop

Active Ingredient:
Levosimendan
Origin:
EU

Levatrop (Levosimendan)

Levosimendan, the active ingredient in Levatrop, is a calcium sensitizer presented as an intravenous infusion for hospital use. It is employed to improve cardiac contractility and reduce vascular resistance in patients experiencing acute decompensated heart failure. The drug acts rapidly when administered by continuous infusion under medical supervision, targeting patients with severe symptoms of heart failure who require hemodynamic support.

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

Manufacturer / TM Owner

Pharmaselect International Beteiligungs Gmbh

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Indications & Clinical Uses

Levosimendan is used in the management of acute heart failure syndromes, where it enhances cardiac performance.

  • Acute decompensated heart failure: improves cardiac output and relieves pulmonary congestion.
  • Severe chronic heart failure (adjunctive therapy): provides temporary hemodynamic support during exacerbations.
  • Low cardiac output syndrome after cardiac surgery: enhances myocardial contractility and facilitates weaning from mechanical support.

How It Works

  • Levosimendan binds to cardiac troponin C, increasing its sensitivity to calcium and thereby augmenting myocardial contractility without raising intracellular calcium levels. Simultaneously, it opens ATP‑sensitive potassium channels in vascular smooth muscle, causing arterial and venous dilation. The combined inotropic and vasodilatory actions lower cardiac preload and afterload, improving overall cardiac efficiency.

Side Effects

Levosimendan may be associated with several adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Headache
  • Nausea
  • Vomiting
  • Hypotension
  • Tachycardia
  • Flushing

Serious or Rare Side Effects

  • Arrhythmias (including ventricular tachycardia)
  • Myocardial ischemia
  • Severe hypotension requiring intervention
  • Allergic reactions (anaphylaxis, rash)
  • Electrolyte disturbances (e.g., hyperkalemia)

Precautions & Warnings

When using Levatrop, clinicians should observe specific safety measures to minimize risk.

  • Patient selection: assess for severe hypotension or obstructive cardiac lesions before initiation.
  • Monitoring: continuously monitor blood pressure, heart rate, and ECG during infusion.
  • Renal function: adjust therapy in patients with impaired renal clearance.
  • Hepatic function: use caution in severe liver disease due to altered metabolism.
  • Concomitant vasodilators: avoid concurrent high‑dose nitrates or phosphodiesterase‑5 inhibitors to prevent excessive hypotension.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levosimendan can interact with other medicines, influencing its efficacy or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma concentrations.
  • Concurrent use with other inotropes (e.g., dopamine, dobutamine) at high doses: risk of excessive cardiac stimulation.
  • Nitrates or phosphodiesterase‑5 inhibitors: can cause profound hypotension.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate hypotensive effects; monitor fluid status.
  • Anticoagulants (e.g., warfarin): monitor INR as hemodynamic changes can affect coagulation.
  • Beta‑blockers: may blunt desired inotropic response; adjust dosing as needed.

Frequently Asked Questions

Levatrop contains levosimendan and is indicated for the treatment of acute decompensated heart failure. It helps improve cardiac output and relieve symptoms such as shortness of breath by enhancing heart muscle contractility and reducing vascular resistance.

Levosimendan sensitises cardiac troponin C to calcium, which strengthens heart‑muscle contraction without increasing intracellular calcium. At the same time it opens ATP‑sensitive potassium channels in blood‑vessel walls, causing vasodilation and lowering the workload on the heart.

The dosing regimen for Levatrop is determined by the prescribing clinician based on the patient’s clinical status, weight, and response to therapy. It is administered as a controlled intravenous infusion in a hospital setting.

Safety data for levosimendan in pregnancy and lactation are limited. The product should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by the treating physician.

To place an order, submit an enquiry on the Levatrop 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 if needed) and import documentation.

Unlike traditional catecholamine inotropes like dobutamine, levosimendan increases contractility by calcium sensitisation rather than raising intracellular calcium, which may reduce the risk of arrhythmias. It also provides vasodilatory effects through potassium‑channel activation, offering combined inotropic and afterload‑reducing benefits.

Levatrop should be stored at 2‑8 °C, protected from light, and kept in its original packaging. It must not be frozen or shaken. If the product reaches room temperature, it should be used promptly according to the manufacturer’s instructions.

Levatrop is given by continuous intravenous infusion under medical supervision. The infusion rate is adjusted by the clinician based on haemodynamic monitoring, and the drug is typically administered in a hospital intensive‑care or cardiac‑care unit.

The most critical adverse events include severe hypotension, life‑threatening arrhythmias such as ventricular tachycardia, and myocardial ischemia. Patients should be closely monitored for changes in blood pressure, heart rhythm and signs of reduced coronary perfusion during treatment.

Levatrop is contraindicated in patients with uncontrolled severe hypotension, obstructive cardiac lesions (e.g., severe aortic stenosis), or known hypersensitivity to levosimendan or any of its excipients. Caution is also advised in individuals with significant renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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