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Oxcarbazepine

    DEA Class;  Rx

    Common Brand Names; Trileptal, Oxtellar XR

    • Anticonvulsants, Other

    Oral anticonvulsant that is a keto-analog of carbamazepine (CBZ); does not require routine drug concentration monitoring
    Indicated for partial seizures in adults and pediatric patients 2 years and older; used off-label for neuropathic pain in adults
    Close monitoring for emerging or worsening suicidal thoughts/behavior or depression recommended

    Indicated for the treatment of partial seizures.

    For the treatment of trigeminal neuralgia.
    For the treatment of mania associated with bipolar disorder.

    Known hypersensitivity to oxcarbazepine or any of its components, or to eslicarbazepine acetate

    • Dizziness (30-50%)
    • Diplopia (30-50%)
    • Headache (26-30%)
    • Nausea/vomiting (26-30%)
    • Nystagmus (26-30%)
    • Somnolence (26-30%)
    • Ataxia (10-30%)
    • Abnormal gait (16-20%)
    • Tremor (16-20%)
    • Abdominal pain (11-15%)
    • Fatigue (11-15%)
    • Vertigo (11-15%)
    • Vision abnormalities (11-15%)
    • Dyspepsia (5-6%)
    • Rash (4%)
    • Insomnia (2-4%)
    • Abnormal thinking (<4%)
    • Hyponatremia (1-3%)
    • Muscle weakness (1-2%)
    • Hypotension (<2%)
    • Speech disorder (1%)
    • Asthenia
    • Angioedema
    • Anaphylaxis
    • Multiorgan immune hypersensitivity reaction
    • Hematic and lymphatic systems: Bone marrow depression, agranulocytosis, aplastic anemia, pancytopenia, neutropenia
    • Digestive system: Pancreatitis and/or lipase and/or amylase increased
    • Metabolism and nutrition disorders: Folic acid deficiency, hypothyroidism
    • Skin and appendages: Erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis
    • Skeletal: Fractures, decreased bone mineral, osteoporosis
    • Body as a whole: Multiorgan hypersensitivity disorders characterized by features such as rash, fever, lymphadenopathy, abnormal liver function tests, eosinophilia, and arthralgia
    • Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS)/Multi-Organ Hypersensitivity

    Hypersensitivity reactions may occur; if signs or symptoms of hypersensitivity develop, discontinue treatment immediately

    Antiepileptic drugs (AEDs) increase risk of suicidal thoughts or behavior in patients receiving therapy; monitor for emergence or worsening of depression, suicidal thoughts or behavior, and/or any unusual changes in mood or behavior

    Caution performing tasks that require mental alertness

    Potentially fatal skin reactions may occur (eg, Stevens-Johnson syndrome)

    Discontinue if dermatological reactions occur

    Significant hyponatremia and syndrome of inappropriate antidiuretic hormone secretion (SIADH) may develop (monitor especially in patients at risk of hyponatremia)

    Pancytopenia, agranulocytosis, and leukopenia reported rarely

    Hypothyroidism reported; monitor thyroid function, especially in children; discontinuation of therapy associated with return of normal thyroxine levels

    Patients carrying the HLA-B*1502 allele may be at increased risk for Stevens-Johnson syndrome and epidermal necrolysis

    Half-life of primary active metabolite is prolonged 3- to 4-fold and AUC is doubled in patients with CrCl <30 mL/min; adjust dose in these patients

    Exacerbation of or new onset of primary generalized seizures reported; risk of aggravation of primary generalized seizures is seen especially in children but may also occur in adults; discontinue therapy if it occurs

    Do not discontinue anticonvulsants abruptly; withdraw gradually because of risk of increased seizure frequency and status epilepticus; if withdrawal is needed because of serious adverse event, rapid discontinuation can be considered

    There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to AEDs, such as TRILEPTAL, during pregnancy. 

    Oxcarbazepine and its active metabolite (MHD) are excreted in human milk

    A milk-to-plasma concentration ratio of 0.5 was found for oxcarbazepine and MHD

    Adults

    2,400 mg/day PO.

    Geriatric

    2,400 mg/day PO.

    Adolescents

    17 years: 2,400 mg/day PO of immediate-release formulations; see individualized age and weight-dependent dosage recommendations for the extended-release tablets.
    13 to 16 years: See individualized age and weight-dependent dosage recommendations.

    Children

    6 to 12 years: See individualized age and weight-dependent dosage recommendations.
    4 to 5 years: See individualized age and weight-dependent dosage recommendations for immediate-release formulations; safety and efficacy of the extended-release tablets not established.
    2 to 3 years: 60 mg/kg/day PO (in 2 divided doses) of immediate-release formulations; safety and efficacy of the extended-release tablets not established.
    Less than 2 years: Safety and efficacy have not been established.

    Infants

    Safety and efficacy have not been established.

    Oxcarbazepine

    tablet, film-coated (Trileptal, generic)

    • 150mg
    • 300mg
    • 600mg

    tablet, extended-release (Oxtellar XR)

    • 150mg
    • 300mg
    • 600mg

    oral suspension (Trileptal, generic)

    • 300mg/5mL