Brivaracetam

Brivaracetam

DEA Class;  Rx

Common Brand Names; Briviact

  • SV2A Ligands

2-pyrrolidine derivative and levetiracetam analog
Used for partial onset seizures in patients 1 month and older
Increased risk of suicidal ideation and behavior

Indicated for the treatment of partial seizures.

Hypersensitivity; bronchospasms and angioedema have occurred

Somnolence and sedation (16%)

Dizziness (12%)

Fatigue (9%)

Nausea and vomiting (5%)

Cerebellar coordination and balance disturbances (3%)

Irritability (3%)

Constipation (2%)

May cause psychiatric adverse reactions, including nonpsychotic and psychotic symptoms; advise patients and caregivers/families to be alert for these behavioral changes and report them to their physician immediately

Hypersensitivity reactions reported, including bronchospasm and angioedema; if a patient develops hypersensitivity reactions after treatment, the drug should be discontinued

If discontinued, withdraw drug gradually because of the risk of increased seizure frequency and status epilepticus; if withdrawal is needed because of a serious adverse event, consider rapid discontinuation

No adequate and well-controlled studies in pregnant women

Unknown if distributed in human breast milk

Adults

200 mg/day PO or IV.

Geriatric

200 mg/day PO or IV.

Adolescents

16 to 17 years: 200 mg/day PO or IV.
13 to 15 years weighing 50 kg or more: 200 mg/day PO or IV.
13 to 15 years weighing 20 to 49 kg: 4 mg/kg/day PO or IV.

Children

weighing 50 kg or more: 200 mg/day PO or IV.
weighing 20 to 49 kg: 4 mg/kg/day PO or IV.
weighing 11 to 19 kg: 5 mg/kg/day PO or IV.
weighing less than 11 kg: 6 mg/kg/day PO or IV.

Infants

weighing 11 to 19 kg: 5 mg/kg/day PO or IV.
weighing less than 11 kg: 6 mg/kg/day PO or IV.

Neonates

Safety and efficacy have not been established.

Brivaracetam

tablet: Schedule V

  • 10mg
  • 25mg
  • 50mg
  • 75mg
  • 100mg

oral solution: Schedule V

  • 10mg/mL

injection, solution: Schedule V

  • 50mg/5mL single-dose vial
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