Product image of Levossimendano Kabi (Levosimendan) supplied by GNH India

Levossimendano Kabi

Active Ingredient:
Levosimendan
Origin:
EU

Levossimendano Kabi (Levosimendan)

Levosimendan, the active ingredient in Levossimendano Kabi, is a calcium sensitizer presented as an injectable solution for intravenous use. It is used to improve cardiac performance in adults with acute decompensated heart failure.
GNH India supplies Levossimendano Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Fresenius Kabi Pharma Portugal, Lda.

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Indications & Clinical Uses

Levosimendan is employed in the management of heart failure syndromes where enhanced contractility is required.

  • Acute decompensated heart failure: increases cardiac output and relieves pulmonary congestion.
  • Severe chronic heart failure (when standard therapy is insufficient): provides additional inotropic support.
  • Heart failure with reduced ejection fraction: helps maintain systemic perfusion during acute decompensation.

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‑sensitive potassium channels in vascular smooth muscle, causing arterial and venous dilation, which reduces cardiac preload and afterload, improving overall cardiac efficiency.

Side Effects

Levosimendan may be associated with a range of adverse reactions.

Common Side Effects

  • Hypotension: mild to moderate blood pressure drop.
  • Headache: transient cranial discomfort.
  • Nausea: occasional upset stomach.
  • Dizziness: feeling light‑headed.
  • Vomiting: occasional emesis.
  • Tachycardia: increased heart rate.

Serious or Rare Side Effects

  • Arrhythmias: potentially life‑threatening rhythm disturbances.
  • Myocardial ischemia: reduced heart muscle blood flow.
  • Severe hypotension: marked blood pressure fall requiring intervention.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Pulmonary edema: fluid accumulation in lungs.
  • Liver enzyme elevation: abnormal hepatic function tests.

Precautions & Warnings

Levosimendan should be used with careful clinical monitoring.

  • Hemodynamic monitoring: continuous blood pressure and ECG assessment.
  • Concomitant vasodilators: avoid excessive hypotension when combined.
  • Pre‑existing arrhythmias: assess risk before initiation.
  • Severe renal or hepatic impairment: dose adjustment may be required.
  • Pregnancy and lactation: safety not established; use only if benefits outweigh risks.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Levosimendan may interact with several drug classes.

Major Interactions (Avoid)

  • Strong vasodilators (e.g., nitroglycerin): risk of profound hypotension.
  • Potassium channel blockers: additive vasodilatory effect.
  • Anti‑arrhythmic agents (e.g., amiodarone): potential for arrhythmia exacerbation.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may blunt desired inotropic response.
  • Diuretics: monitor electrolyte balance and blood pressure.
  • ACE inhibitors/ARBs: watch for additive blood pressure effects.

Frequently Asked Questions

Levossimendano Kabi contains levosimendan, an intravenous calcium sensitizer indicated for the treatment of acute decompensated heart failure in hospitalized adults, where rapid improvement of cardiac output is needed.

Levosimendan enhances the sensitivity of cardiac troponin C to calcium, which strengthens heart muscle contraction without increasing intracellular calcium. It also opens ATP‑sensitive potassium channels in blood vessels, causing vasodilation and reducing the workload on the heart.

The dosing regimen for Levossimendano Kabi is determined by the prescribing clinician based on the patient’s clinical condition, weight, and response. Specific dose and infusion rates are individualized and should follow the prescriber’s instructions.

Safety data for levosimendan in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any 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 (including cold‑chain if needed), and import documentation.

Unlike traditional catecholamine inotropes, levosimendan increases contractility by sensitizing troponin C to calcium and provides vasodilation through potassium‑channel activation, which may result in fewer arrhythmias and less increase in myocardial oxygen consumption.

Levossimendano Kabi should be stored at ambient temperature, below 25 °C, in its original packaging, protected from moisture and direct light. Do not freeze or expose to extreme temperatures.

The product is given intravenously, typically as a loading infusion followed by a continuous maintenance infusion, under close hemodynamic monitoring in a hospital setting. Administration details are defined by the treating physician.

Serious risks include severe hypotension, life‑threatening arrhythmias, myocardial ischemia, and allergic reactions such as anaphylaxis. Patients should be monitored continuously for these events during and after infusion.

Patients with known hypersensitivity to levosimendan or any excipients, those with uncontrolled severe hypotension, recent myocardial infarction, or significant ventricular arrhythmias should not receive the drug unless a specialist determines that benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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