Levosimendan CAS:141505-33-1
Levosimendan is indicated for use in patients with acute decompensated heart failure when standard therapy alone is insufficient. It is administered through intravenous infusion and offers a unique pharmacological profile, combining positive inotropic effects without increasing myocardial oxygen consumption, as well as vasodilatory properties that reduce cardiac preload and afterload. The use of levosimendan is typically initiated in hospital settings under the close supervision of healthcare professionals experienced in managing heart failure. The medication is administered as a continuous intravenous infusion over a specified duration, with dosing adjustments made based on the patient's hemodynamic response. In addition to its inotropic effects, which enhance cardiac contractility, levosimendan also promotes vasodilation in both arterial and venous circulation. By reducing cardiac workload and improving overall cardiac efficiency, it can help alleviate symptoms such as dyspnea and edema in patients experiencing acute episodes of heart failure. Careful monitoring of vital signs, fluid balance, and renal function is essential during levosimendan therapy, as the medication may have an impact on systemic hemodynamics and renal perfusion. Healthcare providers should also evaluate electrolyte imbalances and other potential adverse effects that may arise during treatment. While generally well-tolerated, levosimendan may be associated with adverse effects, such as hypotension, arrhythmias, and headache. Patients receiving levosimendan should be informed about these potential side effects and monitored closely for their occurrence. Overall, the use of levosimendan represents a valuable option for managing acute decompensated heart failure, particularly in instances where conventional therapies may be inadequate. Through its combined inotropic and vasodilatory actions, levosimendan offers a targeted approach to addressing the hemodynamic challenges characteristic of acute heart failure, with the potential to improve clinical outcomes and relieve symptoms in affected individuals. Close collaboration between healthcare providers and patients is crucial in ensuring safe and effective use of levosimendan in the context of acute decompensated heart failure.
Composition | C14H12N6O |
Assay | 99% |
Appearance | white powder |
CAS No. | 141505-33-1 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |