After intravenous administration, the average half-life was 9 hours and the average clearance was 30 l/hour in children 7 to 19 years of age (average age: 12 years)
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No information is present at this moment.
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| Hypertension, prophylaxis for supraventricular tachycardia |
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| Myoclonic epilepsy (Dravet syndrome) |
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| Severe therapy-resistant supraventricular tachycardia |
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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
Hypotension, pulmonary oedema.
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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
Be aware of the possibility of congestive heart failure and combinations with beta-blockers. Can raise digoxin levels significantly. When administering intravenously, calcium gluconate should always be present as the antagonist.
There are cases known of severe (fatal) haemodynamic side effects in children aged < 1 year after intravenous administration of verapamil.
Intravenous administration to children should be done with intensive monitoring and (because of the high risk) it is only justifiable in the treatment of severe refractory supraventricular tachycardia.
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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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