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

Levosimendan Accord

Active Ingredient:
Levosimendan
Origin:
EU

Levosimendan Accord (Levosimendan)

Levosimendan, the active ingredient in Levosimendan Accord, is a calcium sensitizer presented as an injectable solution for intravenous use. It treats acute decompensated heart failure in adult patients.
GNH India supplies Levosimendan Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

Levosimendan is used in the management of heart failure, particularly acute decompensated heart failure.

  • Acute decompensated heart failure: improves cardiac output and relieves symptoms of congestion.
  • Severe left ventricular dysfunction: provides inotropic support when conventional therapy is insufficient.
  • Post‑cardiac surgery low‑output syndrome: helps restore adequate systemic perfusion during the early postoperative period.

How It Works

  • Levosimendan increases cardiac contractility by binding to troponin C and sensitising it to calcium, thereby enhancing the force of myocardial contraction without raising intracellular calcium levels. Simultaneously, it opens ATP‑sensitive potassium channels in vascular smooth muscle, causing vasodilation and reducing both preload and afterload, which together improve cardiac performance.

Side Effects

Levosimendan may be associated with several adverse reactions.

Common Side Effects

  • Headache: mild to moderate intensity, often transient.
  • Hypotension: reduction in blood pressure, especially after rapid infusion.
  • Nausea or vomiting: gastrointestinal discomfort during or after administration.
  • Tachycardia: increased heart rate, usually dose‑related.
  • Dizziness: sensation of light‑headedness, often linked to blood pressure changes.

Serious or Rare Side Effects

  • Ventricular arrhythmias: potentially life‑threatening irregular heart rhythms.
  • Myocardial ischemia: chest pain due to reduced coronary blood flow.
  • Severe hypotension: marked drop in blood pressure requiring intervention.
  • Allergic reactions: rash, pruritus, or anaphylaxis in susceptible individuals.

Precautions & Warnings

Levosimendan should be used with careful clinical monitoring.

  • Blood pressure monitoring: observe for hypotension during infusion.
  • Cardiac rhythm surveillance: watch for arrhythmias, especially in patients with pre‑existing conduction disorders.
  • Renal function assessment: adjust therapy in severe renal impairment.
  • Hepatic impairment caution: consider reduced clearance in liver disease.
  • Contraindication in severe hypotension: avoid use when systolic pressure is markedly low.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Levosimendan can interact with several drug classes, requiring attention to dosing and monitoring.

Major Interactions (Avoid)

  • Concurrent vasodilators (e.g., nitroglycerin): may cause profound hypotension.
  • Strong CYP450 inhibitors (e.g., ketoconazole): can increase plasma concentrations.
  • Potassium‑channel blockers: additive effects on vascular tone.

Moderate Interactions (Monitor Closely)

  • Diuretics: may exacerbate electrolyte shifts and hypotension.
  • Beta‑blockers: may blunt the inotropic response.
  • ACE inhibitors or ARBs: combined effect on blood pressure needs observation.

Frequently Asked Questions

Levosimendan Accord 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 low cardiac output.

Levosimendan works by binding to troponin C, increasing the sensitivity of the heart muscle to calcium, which enhances contractile force without raising intracellular calcium. It also opens ATP‑sensitive potassium channels in vascular smooth muscle, causing vasodilation and lowering cardiac workload.

The dosing regimen for Levosimendan Accord is determined by the prescribing physician based on the patient’s clinical condition, weight, and response. The product is supplied as an injectable solution for intravenous infusion, and the exact dose and infusion rate are individualized.

The safety of Levosimendan Accord in pregnancy and lactation has not been established. 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 a qualified healthcare professional.

To order Levosimendan Accord, 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 without raising intracellular calcium, which may reduce the risk of arrhythmias. It also provides vasodilation through potassium‑channel activation, offering combined inotropic and afterload‑reducing effects that differ from agents such as dobutamine or milrinone.

Levosimendan Accord should be stored at 2‑8 °C in a refrigerator. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution to maintain stability.

Levosimendan Accord is given as an intravenous infusion. The initial loading dose is typically administered over a short period, followed by a continuous maintenance infusion. Administration details, including infusion rate and duration, are set by the treating physician.

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

Levosimendan Accord is contraindicated in patients with severe hypotension, uncontrolled ventricular arrhythmias, or known hypersensitivity to the drug or its excipients. Caution is also advised in individuals with significant renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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