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Oxcarbazepine !

A relative of carbamazepine for focal seizures. Its active metabolite blocks sodium channels; low blood sodium is its typical problem.

Updated 2026-11-01

The figure shows carbamazepine, a close relative that occupies the same site, bound to human Nav1.7 (SCN9A); no structure with oxcarbazepine or its metabolite is available.

Target in 3D: Voltage-gated sodium channel (Nav). PDB structure 8S9C (RCSB PDB, public domain). View the structure at RCSB PDB

Mechanism of action

Oxcarbazepine is quickly reduced to its 10-monohydroxy metabolite (MHD), which does most of the work. Both block voltage-gated sodium channels, stabilizing hyperexcited membranes, inhibiting repetitive firing and reducing the spread of synaptic impulses.

  1. Reduced to the active metabolite MHD
  2. MHD blocks voltage-gated sodium channels
  3. Repetitive neuronal firing is inhibited
  4. Focal seizures do not spread

Pharmacokinetics

Absorption
Absorbed by mouth
Metabolism
Rapidly reduced in the liver to the active metabolite MHD; strong CYP3A4 or UGT inducers lower its levels
Elimination
Mainly kidneys; MHD half-life lengthens in severe kidney disease
Half-life
About 2 hours for oxcarbazepine and about 9 hours for MHD

Indications

Adverse effects

Common

  • Dizziness and sleepiness
  • Double vision and abnormal vision
  • Nausea and vomiting
  • Unsteadiness, tremor and abnormal gait
  • Fatigue and headache

Contraindications

  • Hypersensitivity to oxcarbazepine or to eslicarbazepine acetate

Key interactions

Hormonal contraceptives
Less contraceptive effect
Strong CYP3A4 or UGT inducers (carbamazepine, phenytoin, phenobarbital)
Lower MHD levels
Other drugs that lower sodium, such as those causing inappropriate ADH secretion
More hyponatraemia

What is monitored

  • Serum sodium, especially in the first months and with other sodium-lowering drugs
  • HLA-B*1502 in people with ancestry from at-risk Asian populations
  • Skin and signs of hypersensitivity
  • Mood and suicidal thoughts

Administration and safety

  • Given by mouth as tablets or suspension
  • Immediate- and extended-release forms are not interchangeable without care
  • Withdrawn gradually: stopping suddenly can trigger seizures

Nursing care

  • Ask about previous reactions to carbamazepine
  • Watch for headache, confusion, nausea or more seizures that may signal low sodium
  • Teach to report rash or fever
  • Remind that hormonal contraception may fail

Pregnancy and breastfeeding

MHD levels may fall gradually during pregnancy and recover after delivery, so seizure control is followed closely.

Test yourself

Think of the answer, then tap the question to see it.

What is the active form of oxcarbazepine?

Its 10-monohydroxy metabolite (MHD), which blocks voltage-gated sodium channels and has a longer half-life than the parent drug.

Which electrolyte must be checked during oxcarbazepine treatment?

Sodium: clinically significant hyponatraemia can develop.

Can a patient who had a hypersensitivity reaction to carbamazepine safely switch to oxcarbazepine?

Not without caution: cross-hypersensitivity occurs, and oxcarbazepine is stopped at once if signs appear.

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Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.

Sources: Oxcarbazepine: MedlinePlus Drug Information (MedlinePlus (U.S. National Library of Medicine), 2024); DailyMed - OXCARBAZEPINE tablet, film coated (DailyMed (U.S. National Library of Medicine), 2026); ATCDDD - ATC/DDD Index (WHO Collaborating Centre for Drug Statistics Methodology, 2026).

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Representative model, for educational purposes only.