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

Levosimendan Stada

Active Ingredient:
Levosimendan
Origin:
EU

Levosimendan Stada (Levosimendan)

Levosimendan, the active ingredient in Levosimendan Stada, is a calcium sensitizer presented as an intravenous formulation for intravenous use. It is employed in the management of acute decompensated heart failure to enhance cardiac contractility and support circulation in patients with severe ventricular dysfunction.

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

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Levosimendan is indicated for conditions involving acute cardiac insufficiency where rapid improvement of contractility is required.

  • Acute decompensated heart failure: increases cardiac output and relieves symptoms of low output.
  • Severe left ventricular dysfunction: improves myocardial performance during acute episodes.
  • Post‑cardiac surgery low‑output syndrome: supports hemodynamics when conventional therapy is insufficient.

How It Works

  • Levosimendan binds to cardiac troponin C, increasing its sensitivity to calcium and thereby enhancing contractile force without raising intracellular calcium levels. Simultaneously, it opens ATP‑sensitive potassium channels in vascular smooth muscle, causing vasodilation and reducing cardiac preload and afterload, which together improve overall cardiac performance.

Side Effects

Levosimendan may be associated with several adverse reactions that clinicians monitor during therapy.

Common Side Effects

  • Hypotension: reduction in blood pressure, especially after infusion start.
  • Headache: mild to moderate intensity.
  • Nausea: occasional gastrointestinal upset.
  • Tachycardia: increased heart rate.
  • Dizziness: transient light‑headedness.

Serious or Rare Side Effects

  • Severe hypotension: may require vasopressor support.
  • Arrhythmias: ventricular or atrial ectopic beats.
  • Myocardial ischemia: chest pain or ECG changes.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Pulmonary edema: fluid accumulation in lungs.
  • Liver enzyme elevation: transient increase in transaminases.

Precautions & Warnings

When using Levosimendan, several safety considerations should be observed.

  • Hemodynamic monitoring: continuous blood pressure and cardiac rhythm assessment is essential.
  • Concomitant vasodilators: avoid excessive hypotension by adjusting doses.
  • Pre‑existing arrhythmias: evaluate risk before initiation.
  • Renal or hepatic impairment: consider dose adjustments and close observation.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levosimendan can interact with other medications that affect cardiovascular function.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma concentrations.
  • Concurrent use with other inotropes (e.g., dobutamine): risk of excessive cardiac stimulation.
  • Potent vasodilators (e.g., nitroglycerin): can cause severe hypotension.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate volume depletion and hypotension.
  • Beta‑blockers: may blunt desired inotropic effect.
  • Anticoagulants: monitor for bleeding if hypotension occurs.

Frequently Asked Questions

Levosimendan Stada is used in the acute management of severe heart failure, particularly acute decompensated heart failure, to improve cardiac contractility and support circulation during critical episodes.

Levosimendan increases the sensitivity of cardiac troponin C to calcium, enhancing contractile force without raising intracellular calcium. It also opens ATP‑sensitive potassium channels in vascular smooth muscle, causing vasodilation and reducing cardiac workload.

The dosing regimen for Levosimendan Stada is determined by the prescribing clinician based on the patient’s clinical condition, weight, and response. Specific dose instructions are provided in the product’s prescribing information.

Levosimendan should only be used during pregnancy or lactation if the potential benefit outweighs any possible risk to the fetus or infant. Safety data are limited, so a careful risk‑benefit assessment by the healthcare provider is required.

To place an order, 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.

Unlike traditional catecholamine inotropes, levosimendan enhances contractility by sensitizing troponin C to calcium and provides vasodilation through potassium‑channel activation, which may result in fewer arrhythmias and a longer duration of action after infusion.

Levosimendan Stada should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Maintaining the cold‑chain ensures product stability and efficacy.

Levosimendan Stada is given as an intravenous infusion under continuous hemodynamic monitoring. The infusion rate and duration are set by the treating physician according to the patient’s response.

Serious risks include severe hypotension, life‑threatening arrhythmias, myocardial ischemia, and allergic reactions such as anaphylaxis. Prompt recognition and management of these events are essential during therapy.

Patients with uncontrolled severe hypotension, known hypersensitivity to levosimendan or its excipients, or those receiving contraindicated vasodilators should not be treated with Levosimendan Stada. Clinical judgment is required for each individual case.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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