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 improve cardiac contractility and reduce symptoms in hospitalized patients.

GNH India supplies Levosimendan Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and intensive‑care units worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

  • Levosimendan is indicated for conditions affecting cardiac output and systemic perfusion.
  • Acute decompensated heart failure: improves cardiac output and relieves congestion.
  • Low cardiac output syndrome: enhances myocardial contractility without increasing intracellular calcium.
  • Post‑cardiac surgery ventricular dysfunction: supports hemodynamics during early postoperative period.

How It Works

  • Levosimendan binds to cardiac troponin C, increasing its sensitivity to calcium and thereby augmenting contractile force without raising intracellular calcium levels. Simultaneously, it opens ATP‑sensitive potassium channels in vascular smooth muscle, causing vasodilation and reducing after‑load, 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: drop in blood pressure, especially after rapid infusion.
  • Headache: mild to moderate intensity.
  • Nausea or vomiting: gastrointestinal discomfort.
  • Dizziness or light‑headedness.
  • Tachycardia: increased heart rate.
  • Peripheral edema: swelling of extremities.

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: worsening respiratory status.
  • Liver enzyme elevation: abnormal hepatic function tests.

Precautions & Warnings

  • Levosimendan requires careful patient assessment and monitoring before and during administration.
  • Cardiovascular monitoring: continuous blood pressure and heart‑rate observation is essential.
  • Renal impairment: use with caution in severe renal dysfunction; dose adjustment may be needed.
  • Hepatic impairment: consider reduced dosing in patients with significant liver disease.
  • Concomitant vasodilators: may potentiate hypotensive effects; adjust therapy accordingly.
  • Electrolyte disturbances: correct hypokalemia or hypomagnesemia before infusion.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Levosimendan can interact with several drug classes, influencing its safety profile.

Major Interactions (Avoid)

  • Sodium nitroprusside: additive hypotensive effect.
  • Phosphodiesterase‑5 inhibitors: risk of severe blood‑pressure fall.
  • Other calcium sensitizers: unknown synergistic actions.

Moderate Interactions (Monitor Closely)

  • Loop diuretics: may alter intravascular volume status.
  • ACE inhibitors or ARBs: monitor for excessive hypotension.
  • Anticoagulants: observe for increased bleeding tendency.

Frequently Asked Questions

Levosimendan Stada is used in the hospital setting to treat acute decompensated heart failure. It improves cardiac contractility and reduces vascular resistance, helping patients with low cardiac output regain stable hemodynamics.

Levosimendan sensitizes cardiac troponin C to calcium, which enhances myocardial contraction without raising intracellular calcium. It also opens ATP‑sensitive potassium channels in vascular smooth muscle, producing vasodilation and lowering after‑load.

The dosing regimen for Levosimendan Stada is determined by the prescribing physician based on the patient’s clinical condition, weight, and response. The product is administered intravenously under continuous monitoring.

Safety data for levosimendan in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential 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 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 increases contractility without raising intracellular calcium, which may reduce arrhythmic risk. It also provides vasodilation through potassium‑channel activation, offering a dual mechanism that can be advantageous in certain heart‑failure patients.

Levosimendan Stada should be stored at 2‑8 °C, protected from light, and must not be frozen. The product should be kept in its original packaging until reconstitution and used within the stability period indicated by the manufacturer.

Levosimendan Stada is given as an intravenous infusion, typically initiated with a loading dose followed by a continuous maintenance infusion. Administration is performed in a monitored setting, such as an intensive‑care unit, with regular assessment of hemodynamic parameters.

Serious risks include severe hypotension, life‑threatening arrhythmias, myocardial ischemia, and allergic reactions. Patients should be closely monitored for blood‑pressure changes, cardiac rhythm disturbances and signs of allergic response throughout the infusion.

Levosimendan is contraindicated in patients with known hypersensitivity to the drug, severe hypotension unresponsive to treatment, and those receiving other potent vasodilators that could precipitate dangerous blood‑pressure drops. Clinical judgment is required for patients with severe hepatic or renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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