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

Levossimendano Accord

Active Ingredient:
Levosimendan
Origin:
EU

Levossimendano Accord (Levosimendan)

Levosimendan, the active ingredient in Levossimendano Accord, is a calcium sensitizer and inotropic agent presented as an injection solution for intravenous use. It is indicated for the rapid management of acute decompensated heart failure and cardiogenic shock in hospitalized adult patients, improving cardiac output without markedly raising intracellular calcium levels.

GNH India supplies Levossimendano Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide, providing reliable access to this essential cardiovascular therapy.

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

  • Levosimendan is used in the management of acute heart failure syndromes where enhanced cardiac contractility is required.
  • Acute decompensated heart failure: improves hemodynamics and reduces symptoms of congestion.
  • Cardiogenic shock: supports systemic perfusion while lowering afterload.
  • Severe left ventricular dysfunction: provides temporary hemodynamic support during critical illness.

How It Works

  • Levosimendan binds to cardiac troponin C, increasing its sensitivity to calcium and thereby enhancing myocardial contractility without a rise in intracellular calcium concentration. Simultaneously, it activates ATP‑sensitive potassium channels in vascular smooth muscle, leading to vasodilation and reduced cardiac afterload, which together improve overall cardiac output.

Side Effects

Levosimendan may cause a range of adverse reactions that clinicians monitor during therapy.

Common Side Effects

  • Hypotension: drop in blood pressure, especially during loading dose.
  • Headache: mild to moderate intensity.
  • Nausea or vomiting: gastrointestinal discomfort.
  • Tachycardia: increased heart rate.

Serious or Rare Side Effects

  • Ventricular arrhythmias: potentially life‑threatening rhythm disturbances.
  • Myocardial ischaemia: chest pain or ECG changes indicating reduced blood flow.
  • Severe hypotension: profound blood pressure fall requiring intervention.
  • Allergic reactions: rash, bronchospasm, or anaphylaxis.

Precautions & Warnings

  • Before initiating Levossimendano Accord, clinicians should consider several safety measures.
  • Monitor blood pressure: watch for hypotension during infusion.
  • Observe cardiac rhythm: detect arrhythmias early.
  • Use cautiously in severe renal impairment: adjust monitoring as clearance may be affected.
  • Avoid in patients with known hypersensitivity to levosimendan or excipients.
  • Assess hepatic function: consider dose adjustment in severe liver disease.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levosimendan can interact with other medications, requiring careful assessment.

Major Interactions (Avoid)

  • Concurrent use with other potent vasodilators: risk of profound hypotension.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase levosimendan plasma levels.
  • Co‑administration with other calcium sensitizers or inotropes: additive cardiac effects.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may blunt therapeutic response.
  • Diuretics: can exacerbate electrolyte shifts and volume depletion.
  • Anticoagulants: hypotension may affect organ perfusion, influencing bleeding risk.

Frequently Asked Questions

Levossimendano Accord is an intravenous formulation of levosimendan indicated for the rapid treatment of acute decompensated heart failure and cardiogenic shock in hospitalized adults, helping to improve cardiac output and relieve symptoms.

Levosimendan sensitises cardiac troponin C to calcium, enhancing contractile force without raising intracellular calcium, and opens ATP‑sensitive potassium channels in vascular smooth muscle, producing vasodilation and reducing afterload.

The dosing regimen is determined by the prescribing clinician based on the patient’s clinical status, weight, and hemodynamic parameters; the product is supplied as an injectable solution for intravenous infusion under medical supervision.

Safety data are limited; levosimendan is generally avoided during pregnancy and lactation unless the potential benefit justifies the risk, and the decision should be made by a qualified healthcare professional.

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 necessary import documentation.

Unlike catecholamine inotropes, levosimendan increases contractility by calcium sensitisation rather than raising intracellular calcium, which may reduce the risk of arrhythmias; it also provides vasodilation through potassium‑channel activation, offering a distinct haemodynamic profile compared with drugs such as dobutamine or milrinone.

The product should be stored refrigerated at 2–8 °C, protected from light, and must not be frozen or shaken; keep the vial in its original packaging until use to maintain stability.

Levossimendano Accord is given as an intravenous infusion, typically initiated with a loading dose followed by a continuous maintenance infusion, administered by qualified medical personnel in a monitored clinical setting such as an intensive care unit or cardiac care unit.

Serious adverse events include severe hypotension, ventricular arrhythmias, myocardial ischaemia, and rare allergic reactions; patients should be closely monitored for blood pressure, cardiac rhythm and signs of ischemia throughout the infusion.

Contra‑indications include patients with known hypersensitivity to levosimendan or its excipients, those with severe hypotension unresponsive to treatment, and individuals with significant obstructive cardiac outflow lesions; use is also cautioned in severe hepatic or renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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