Active Ingredient: Piracetam
Treatment of cortical myoclonus, should be used in combination with other anti-myoclonic therapies.
For this indication, competent medicine agencies globally authorize below treatments:
Regimen A: Oral, between 7.2 grams piracetam and 20 grams piracetam, divided daily, 2 to 4 doses in total.
Regimen B: Intravenous, in total between 7.2 grams piracetam and 24 grams piracetam, daily.
Regimen C: Parenteral, in total between 7.2 grams piracetam and 24 grams piracetam, daily.
The daily dosage should begin at 7.2 g, increasing by 4.8 g every three or four days up to a maximum of 20 g/day, in two or three sub-doses.
Treatment with other anti-myoclonic medicinal products should be maintained at the same dosage. Depending on the clinical benefit obtained, the dosage of other such medicinal products should be reduced, if possible.
Once started, treatment with piracetam should be continued for as long as the original cerebral disease persists. In patients with an acute episode, spontaneous evolution may occur over time and an attempt should be made every 6 months to decrease or discontinue the medicinal treatment. This should be done by reducing the dose of piracetam by 1.2g every two days (every three or four days in the case of a Lance and Adams syndrome, in order to prevent the possibility of sudden relapse or withdrawal seizures).
When parenteral administration is needed (e.g. swallowing difficulties, unconsciousness) piracetam can be administered intravenously at the same recommended daily dose.
Adjustment of the dose is recommended in elderly patients with compromised renal function. For long term treatment in the elderly, regular evaluation of the creatinine clearance is required to allow dosage adaptation if needed.
Piracetam administered orally may be taken with or without food.
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