There is only a single pharmacokinetic study known in children. That study shows that the elimination half-life in children is 2.5-6.7 hours (N = 13, ages 4 to 22 years). The therapeutic plasma concentration is 2-5 mg/l.
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No information is present at this moment.
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| Brugada syndrome |
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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.
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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
Conduction disorders, extension of the QTc interval, bradycardia, hypotension, gastrointestinal problems, hypersensitivity reaction (fever, vision disorders haematological abnormalities), tinnitus.
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
In class I G6PD deficiency, haemolytic reactions may possibly occur (Dutch Association for Paediatric Medicine (NVK) haematology workbook)
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Adjust the dosage under ECG monitoring; have the serum levels measured if necessary. Hypokalaemia should be corrected beforehand. Because of the risk of hypersensitivity reactions, a test dose is often given first.
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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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| Antiarrhythmics, class Ia | ||
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| C01BA02 | ||
| Antiarrhythmics, class Ic | ||
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| C01BC04 | ||
| C01BC03 | ||
| Antiarrhythmics, class III | ||
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| C01BD01 | ||
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