There are only two studies in which the pharmacokinetics of levosimendan in children have been described. The study by Turanlahti et al. (single administration of 12 µg/kg in children aged 3 months – 7 yrs, n = 13) concludes that the pharmacokinetic profiles of levosimendan in adults and in children are comparable. The following values have been found:
| 3-6 months (n=5) | 6 months to 7 years (n=7) | |
|---|---|---|
| Cmax (ng/ml) | 56.9 | 59.4 |
| Cl (ml/min/kg) | 3.8 | 3.6 |
| Vd in the steady state (l/kg) | 0.43 | 0.35 |
| t½ (hours) | 2.3 | 1.6 |
The pharmacokinetics of the active metabolite were not investigated in the studies.
The study by Pellicer et al. states a Cmax for neonates averaging 16.5 ng/ml, a Tmax averaging 48 hours and a Cl/F averaging 0.67 l/h/kg.
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| In acute heart failure if the standard therapy is not sufficiently effective |
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No data is known about dosage adjustments for renal function disorders. In adults, an improvement in the renal function was seen on the one hand, but on the other caution is needed because of a possibly elevated exposure to active metabolites.
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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
The ECG, blood pressure, heart rate, cardiac output, filling pressure and urine production should be monitored during administration and for at least 3 days after discontinuing or in the case of hepatic or renal function disorders for at least 5 days or until the patient is stable. Any low serum potassium concentration should be corrected before administration and the potassium level should be monitored during administration. Severe hypovolaemia, ventricular tachycardia and paroxysmal tachycardia that is not the result of reperfusion or life-threatening arrhythmia should be corrected before administration.
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The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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| Adrenergic and dopaminergic agents | ||
|---|---|---|
| C01CA24 | ||
| C01CA07 | ||
| C01CA04 | ||
| C01CA26 | ||
| C01CA02 | ||
| C01CA17 | ||
| C01CA24 | ||
| C01CA03 | ||
| C01CA06 | ||
| Phosphodiesterase inhibitors | ||
|---|---|---|
| C01CE02 | ||
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