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 presented as an intravenous formulation for intravenous use. It treats acute decompensated 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 Pharmaceuticals S.A.

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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 and relieves symptoms of congestion.
  • Severe left‑ventricular systolic dysfunction: enhances contractility and reduces filling pressures.
  • Post‑cardiac surgery low‑output syndrome: supports hemodynamics when conventional therapy is insufficient.

How It Works

  • Levosimendan increases cardiac contractility by binding to troponin C and sensitizing it to calcium, which enhances the force of myocardial contraction without raising intracellular calcium levels. It also opens ATP‑sensitive potassium channels in vascular smooth muscle, causing vasodilation and reducing after‑load, thereby improving overall cardiac output.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Hypotension: often transient during infusion.
  • Nausea or vomiting: gastrointestinal discomfort.
  • Tachycardia: increased heart rate.
  • Dizziness: related to blood pressure changes.
  • Flushing: warm sensation on skin.

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.
  • Pulmonary edema: worsening respiratory status.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Liver enzyme elevation: abnormal hepatic function tests.

Precautions & Warnings

  • When administering Levosimendan, several safety considerations should be observed.
  • Cardiovascular monitoring: continuously monitor blood pressure and heart rate during infusion.
  • Renal impairment: adjust infusion rate or consider alternative therapy in severe renal dysfunction.
  • Hepatic impairment: use with caution in patients with significant liver disease.
  • Concomitant vasodilators: avoid excessive hypotension by adjusting doses.
  • Electrolyte disturbances: correct potassium and magnesium abnormalities before starting therapy.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Levosimendan can interact with other cardiovascular agents, requiring careful management.

Major Interactions (Avoid)

  • Sodium nitroprusside: additive hypotensive effect.
  • Phosphodiesterase inhibitors (e.g., milrinone): risk of severe hypotension.
  • Beta‑blockers: may blunt the intended inotropic response.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: monitor for excessive blood pressure drop.
  • Diuretics: watch electrolyte levels and volume status.
  • Calcium channel blockers: observe for bradycardia or conduction abnormalities.

Frequently Asked Questions

Levosimendan Altan is indicated for the treatment of acute decompensated heart failure in adult patients. It is administered intravenously to improve cardiac contractility and reduce symptoms associated with sudden worsening of heart function.

Levosimendan works by sensitizing cardiac troponin C to calcium, which enhances the strength of heart muscle contraction without increasing intracellular calcium. It also opens ATP‑sensitive potassium channels in vascular smooth muscle, causing vasodilation and lowering cardiac after‑load.

The dosing regimen for Levosimendan Altan is determined by the prescribing physician based on the patient’s clinical condition, weight, and response to therapy. Healthcare professionals set the infusion rate and duration according to approved guidelines.

Safety data for Levosimendan in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

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 inotropes that increase intracellular calcium, Levosimendan enhances contractility by calcium sensitization and adds vasodilatory effects through potassium‑channel activation. This dual action can improve cardiac output while potentially causing less arrhythmogenic risk compared with agents such as dobutamine.

Levosimendan Altan should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen. The solution should be kept in its original container until use and handled with aseptic technique to maintain sterility.

Levosimendan Altan is given as an intravenous infusion, typically initiated with a loading dose followed by a continuous maintenance infusion. Administration is performed in a monitored clinical setting where vital signs can be observed continuously.

The most serious risks include severe hypotension, ventricular arrhythmias, and myocardial ischemia. Patients should be closely monitored for blood pressure drops, rhythm changes, and signs of chest pain during and after the infusion.

Levosimendan is contraindicated in patients with known hypersensitivity to the drug, uncontrolled severe hypotension, or those receiving other potent vasodilators that could cause dangerous blood pressure reductions. Clinicians should evaluate each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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