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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