Active Ingredient: Rufinamide
Rufinamide is indicated as adjunctive therapy in the treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 1 year of age and older.
For this indication, competent medicine agencies globally authorize below treatments:
Oral
400 - 3,200 mg
From 200 To 1,600 mg 2 time(s) per day every day
400 mg
Treatment should be initiated at a daily dose of 400 mg. According to clinical response and tolerability, the dose may be increased by 400 mg/day increments, as frequently as every other day, up to a maximum recommended dose as indicated in the table below.
Weight range | 30.0–50.0 kg | 50.1–70.0 kg | ≥70.1 kg |
Maximum recommended dose | 1,800 mg/day | 2,400 mg/day | 3,200 mg/day |
Doses of up to 4,000 mg/day (in the 30-50 kg range) or 4,800 mg/day (in the over 50 kg) have been studied in a limited number of patients.
Treatment should be initiated at a daily dose of 400 mg. According to clinical response and tolerability, the dose may be increased by 400 mg/day increments, as frequently as every other day, up to a maximum recommended dose as indicated in the table below.
Weight range | 30.0–50.0 kg | 50.1–70.0 kg | ≥70.1 kg |
Maximum recommended dose | 1,200 mg/day | 1,600 mg/day | 2,200 mg/day |
Rufinamide should be administered with food.
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