GNH USA

Europe — EMA

Levosimendán Zentiva

GNH USA supplies Levosimendán Zentiva (Levosimendan), a calcium sensitizer for acute decompensated heart failure and cardiogenic shock.

Levosimendan

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What is Levosimendan?

Levosimendan, the active ingredient in Levosimendán Zentiva, is a calcium sensitizer presented as an intravenous solution for intravenous use. It is indicated for acute decompensated heart failure and cardiogenic shock in hospitalized patients, where it improves cardiac contractility and systemic perfusion.

GNH USA supplies Levosimendán Zentiva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and clinics worldwide.

What is Levosimendan used for?

Levosimendan is used in the management of severe cardiac conditions that require rapid improvement of contractility and vascular tone.

Acute decompensated heart failure: enhances cardiac output and relieves congestion. Cardiogenic shock: stabilises haemodynamics and supports organ perfusion.

What are the side effects of Levosimendan?

Levosimendan may be associated with a range of adverse reactions that vary in frequency and severity.

Common Side Effects: - Hypotension: reduction in blood pressure, especially after infusion start. - Headache: mild to moderate intensity. - Nausea: occasional gastrointestinal upset. - Flushing: transient warmth and reddening of skin. - Tachycardia: increased heart rate. - Arrhythmia: non‑sustained ventricular ectopy.

Serious or Rare Side Effects: - Severe hypotension: marked drop in blood pressure requiring intervention. - Ventricular arrhythmias: sustained tachyarrhythmias. - Myocardial ischaemia: chest pain or ECG changes. - Allergic reactions: rash, pruritus, or anaphylaxis. - Liver enzyme elevation: increased transaminases. - Electrolyte disturbances: significant shifts in potassium or magnesium.

What precautions apply to Levosimendan?

Levosimendan should be administered with careful clinical monitoring and awareness of specific safety considerations.

Monitor blood pressure: watch for hypotension during and after infusion. Assess renal function: adjust use in severe renal impairment. Evaluate electrolytes: correct potassium and magnesium abnormalities before administration. Use cautiously after recent myocardial infarction: risk of ischaemia may be increased. Avoid in severe baseline hypotension: may exacerbate low blood pressure. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Levosimendan interact with?

Levosimendan can interact with other cardiovascular agents, requiring attention to dosage and patient status.

Major Interactions (Avoid): - Concurrent vasodilators (e.g., nitroglycerin): may cause profound hypotension. - Strong CYP3A4 inhibitors (e.g., ketoconazole): increase plasma concentrations. - Other inotropes (e.g., dobutamine): risk of excessive cardiac stimulation.

Moderate Interactions (Monitor Closely): - Diuretics: may amplify electrolyte shifts. - ACE inhibitors or ARBs: additive blood‑pressure lowering effect. - Beta‑blockers: may blunt desired inotropic response. - Calcium‑channel blockers: potential for altered vascular tone. - Anti‑arrhythmic drugs: monitor rhythm changes.

Frequently asked questions

What conditions is Levosimendán Zentiva used for?+
Levosimendán Zentiva is indicated for the treatment of acute decompensated heart failure and cardiogenic shock in hospitalized patients. In these settings it helps improve cardiac contractility and systemic perfusion, supporting patients who are experiencing severe circulatory compromise.
How does levosimendan work in the body?+
Levosimendan sensitises cardiac troponin C to calcium, which enhances myocardial contractility without increasing intracellular calcium levels. At the same time it opens ATP‑sensitive potassium channels in vascular smooth muscle, causing arterial and venous dilation that lowers preload and afterload, thereby improving overall cardiac efficiency.
What is the usual dose of Levosimendán Zentiva?+
The dose of Levosimendán Zentiva is determined by the prescribing clinician based on the patient’s clinical status, weight, and response to therapy. The product is supplied as an intravenous solution that is administered under continuous medical supervision in a hospital or intensive‑care setting.
Is Levosimendán Zentiva safe during pregnancy or breastfeeding?+
The safety of levosimendan in pregnancy and lactation has not been established. It is classified as pregnancy category unknown, and the drug should only be used if the potential benefit justifies any potential risk to the fetus or infant. Breastfeeding mothers should consult their healthcare provider.
How do I order Levosimendán Zentiva from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain handling if needed), and the necessary import documentation.
How does Levosimendán Zentiva compare with other inotropes?+
Unlike traditional 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 combined inotropic and afterload‑reducing effect that some clinicians find advantageous in acute heart‑failure settings.
What are the storage and handling requirements for Levosimendán Zentiva?+
Levosimendán Zentiva must be stored refrigerated at 2‑8 °C. The solution should be kept in its original container, protected from light, and must not be frozen or shaken. If the product reaches room temperature, it should be used promptly and not re‑refrigerated.
How is Levosimendán Zentiva administered?+
The medication is supplied as an intravenous solution and is administered by a healthcare professional through a controlled infusion. The infusion rate and duration are set by the treating physician, who monitors haemodynamic parameters throughout the treatment.
What are the most serious risks associated with Levosimendán Zentiva?+
The most serious risks include severe hypotension, ventricular arrhythmias, myocardial ischaemia, and rare allergic reactions such as anaphylaxis. Continuous cardiac and blood‑pressure monitoring is essential during infusion to detect and manage these events promptly.
Who should not receive Levosimendán Zentiva?+
Levosimendán Zentiva should be avoided in patients with uncontrolled severe hypotension, known hypersensitivity to levosimendan or any excipients, and in those with recent acute myocardial infarction where the risk of ischaemia outweighs benefit. Clinical judgment is required for each individual case.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Levosimendan
Route
Intravenous Use
Manufacturer
Zentiva, K.S.
Origin
EU

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