Classes
DEA Class; Rx
Common Brand Names; Trileptal, Oxtellar XR
- Anticonvulsants, Other
Description
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
Indications
Indicated for the treatment of partial seizures.
Contraindications
Known hypersensitivity to oxcarbazepine or any of its components, or to eslicarbazepine acetate
Adverse Effects
- 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
Warnings
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
Pregnancy and Lactation
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
Maximum Dosage
2,400 mg/day PO.
2,400 mg/day PO.
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.
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.
Safety and efficacy have not been established.
How supplied
Oxcarbazepine
tablet, film-coated (Trileptal, generic)
- 150mg
- 300mg
- 600mg
tablet, extended-release (Oxtellar XR)
- 150mg
- 300mg
- 600mg
oral suspension (Trileptal, generic)
- 300mg/5mL