Europe — EMA
Levosimendan Stada
GNH USA supplies Levosimendan Stada (Levosimendan), a calcium sensitizer for acute decompensated heart failure. Request a quote for global supply.
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What is Levosimendan?
Levosimendan, the active ingredient in Levosimendan Stada, is a calcium sensitizer presented as an intravenous formulation for intravenous use. It is employed in the management of acute decompensated heart failure to improve cardiac contractility without increasing intracellular calcium levels. GNH USA supplies Levosimendan Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.
What is Levosimendan used for?
Levosimendan is indicated for acute decompensated heart failure, where it helps restore adequate cardiac output and relieve symptoms of congestion.
Acute decompensated heart failure: improves myocardial contractility and reduces systemic vascular resistance, supporting hemodynamic stability.
What are the side effects of Levosimendan?
Levosimendan may be associated with several adverse reactions that clinicians monitor during therapy.
Common Side Effects: - Hypotension: reduction in blood pressure, especially with rapid infusion. - Headache: mild to moderate intensity. - Nausea or vomiting: gastrointestinal discomfort. - Tachycardia: increased heart rate. - Dizziness or light‑headedness. - Flushing: warmth and reddening of skin.
Serious or Rare Side Effects: - Arrhythmias: ventricular or atrial ectopic beats. - Myocardial ischemia: chest pain due to reduced coronary perfusion. - Severe hypotension: may require vasopressor support. - Pulmonary edema: worsening fluid accumulation in lungs. - Allergic reactions: rash, pruritus, or anaphylaxis. - Liver enzyme elevation: transient increase in hepatic transaminases.
What precautions apply to Levosimendan?
When using Levosimendan, several safety considerations should be observed.
Hemodynamic monitoring: continuous blood pressure and cardiac rhythm assessment is essential. Renal impairment: dose adjustment may be required in severe dysfunction. Electrolyte balance: correct hypokalemia or hypomagnesemia before infusion. Concomitant vasodilators: avoid simultaneous high‑dose nitrates to prevent profound hypotension. Pregnancy and lactation: use only if the potential benefit justifies the potential risk. 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 medicines, influencing its safety and efficacy.
Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma concentrations. - Concurrent potent vasodilators (e.g., high‑dose nitrates, hydralazine): risk of severe hypotension. - Phosphodiesterase‑5 inhibitors (e.g., sildenafil): additive vasodilatory effect.
Moderate Interactions (Monitor Closely): - CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic levels. - Beta‑blockers: may blunt the positive inotropic response. - Diuretics: monitor electrolytes and volume status closely.
Frequently asked questions
What is Levosimendan Stada used for?+
How does levosimendan work?+
What is the usual dose of Levosimendan Stada?+
Is Levosimendan Stada safe during pregnancy or breastfeeding?+
How do I order Levosimendan Stada from GNH USA?+
How does Levosimendan compare with other inotropic agents?+
What are the storage and handling requirements for Levosimendan Stada?+
How is Levosimendan Stada administered?+
What are the most serious risks associated with Levosimendan Stada?+
Who should not receive Levosimendan Stada?+
Product details
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