There is no information available about the pharmacokinetics of this drug in children.
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No information is present at this moment.
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No information is present at this moment.
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| Treatment of uncomplicated urinary tract infections |
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| Prophylaxis of recurrent urinary tract infections |
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| Short-term prophylaxis in procedures on the urinary tract (catheterization or diagnostics) |
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Adjustment in renal impairment as specified:
Accumulation in blood and tissue can cause peripheral neuropathy. Paraesthesia (with tingling or a numb sensation) and weakness have been reported, mostly a few days after starting the treatment. In that case, stop the treatment. Sometimes this leads to peripheral polyneuropathy, usually within 2 months. It can be irreversible and even fatal. Nitrofurantoin is concentrated in the urine, causing bactericidal concentrations there. In creatinine clearances of less than 50 ml/min, this bactericidal concentration becomes smaller and at clearances of less than 30 ml/min, no bactericidal concentration occurs in urine, with therapeutic failure as a result.
Contraindicated
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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
Gastrointestinal side effects occur most often. Side effects may occur less commonly in children than in adults. This may be due to the lower dosages and the lack of comorbidity/co-medication. Paraesthesia. Peripheral neuropathy, which can be severe or irreversible, can also occur (usually within 2 months). This can be life-threatening. The treatment should then be discontinued immediately.
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
Do not use in neonates (< 1 month) because of the immature erythrocyte-enzyme systems.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
A macrocrystalline formulation is preferred. The macrocrystalline form (=MC) has a slower dissolving and absorption rate than the microcrystalline form and therefore gives fewer stomach pains.
Stop the treatment immediately if peripheral neuropathy occurs (mostly within 2 months).
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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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| Glycopeptide antibacterials | ||
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| J01XA01 | ||
| Polymyxins | ||
|---|---|---|
| J01XB01 | ||
| Other antibacterials | ||
|---|---|---|
| J01XX08 | ||
| J01XX01 | ||
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