There is no information about the pharmacokinetic parameters for mannitol in children.
No information is present at this moment.
No information is present at this moment.
| Improvement of hemodynamic stability during hemodialysis (HD) |
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| Reduction of intracranial or intraocular pressure, acute renal insufficiency |
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GFR ≥10 ml/min/1.73m2: Dose adjustment not required.
GFR <10 ml/min/1.73m2: A general recommendation on dose adjustment cannot be provided.
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
No information is present at this moment.
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
Mannitol may accumulate after several doses causing a reverse osmotic effect. The serum osmolality must remain below 320 mOsmol/kg due to the risk of acute renal failure. When administered rapidly there may possibly be a temporary increase in cerebral blood flow (CBF) and intracranial pressure. At low temperatures and particularly at higher concentrations, crystallization can occur; use a 5-micron filter. Monitor for abnormal electrolyte balance and for signs of pulmonary congestion and cardiac failure. Watch out for anuria.
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.
| Solutions affecting the electrolyte balance | ||
|---|---|---|
| B05BB01 | ||