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Licarbazepine

Antiseizure agent (active monohydroxy metabolite / dibenzazepine) · Epilepsy

START
Eslicarbazepine 400 mg PO once daily, titrate
TYPICAL MAX
1600 mg/day
STOP IF
Severe rash, symptomatic hyponatraemia, or hypersensitivity
WATCH
Serum sodium, skin, ECG (PR); HLA-B*1502 in at-risk ancestry
CDSCO approvedSchedule HATC N03AF
Dose laddermg/d
400start800usual1.6kmax/day
Renal dose adjustmenteGFR mL/min/1.73m²
FULLUsual titration30REDUCEReduce dose / extend titration90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1hONSET2.5hPEAK16h1dDURATION
ONSET
1h · absorption
PEAK
2.5h · Tmax
16h ·
DURATION
1d · once-daily
EXCRETION
Renal — glucuronide and unchanged
route + CYP
INTERACTIONS
none in our sources
PREGNANCY
Use only if clearly needed; antiseizure-drug fetal risk — specialist management.
FDA category + note

Mechanism

The active monohydroxy derivative (licarbazepine; eslicarbazepine is its S-enantiomer) blocks voltage-gated sodium channels, stabilising hyperexcited neuronal membranes and limiting repetitive firing — the principal active species of oxcarbazepine.

Indications

Focal (partial-onset) seizures (as active metabolite of oxcarbazepine / eslicarbazepine acetate)

Dosing

Adult
As eslicarbazepine acetate: 400 mg PO once daily, titrate to 800–1600 mg once daily. (As oxcarbazepine metabolite — dosing governed by parent drug.)
Pediatric
Eslicarbazepine ≥4 y: weight-based titration (specialist).
Renal adjustment
CrCl <30: reduce dose / extend titration (renally cleared metabolite).
Hepatic adjustment
Severe hepatic impairment: not recommended (limited data).
Geriatric
Lower doses; hyponatraemia risk.
Max dose
1600 mg/day (as eslicarbazepine acetate)

Pharmacokinetics

Onset
Seizure control over days of titration
Peak effect
~2–3 h (eslicarbazepine acetate Tmax to active species)
Duration
~24 h (once-daily)
Half-life
~13–20 h
Bioavailability
>90% (as eslicarbazepine acetate)
Protein binding
~30%
Metabolism
Minimal further metabolism; glucuronidation
Excretion
Renal (mainly as glucuronide and unchanged)

Contraindications

  • Hypersensitivity to oxcarbazepine/eslicarbazepine/carbamazepine
  • Second/third-degree AV block (eslicarbazepine)
  • Caution: hyponatraemia, HLA-B*1502 (SCAR risk)

Side effects

Common
DizzinessSomnolenceHeadacheDiplopiaNauseaHyponatraemia
Serious
  • Severe hyponatraemia
  • Serious skin reactions (SJS/TEN, DRESS)
  • Hypersensitivity multi-organ reaction
  • PR-interval prolongation

Pregnancy & lactation

Pregnancy

Use only if clearly needed; antiseizure-drug fetal risk — specialist management.

Lactation

Excreted in milk; monitor infant for sedation/poor feeding.

Drug interactions

Carbamazepine
Moderate
Database

Mutual metabolic effects

Monitor levels and tolerability

Source: Kimi deep-research + Cla

Cns Depressants
Moderate
Database

Additive CNS depression

Counsel; avoid alcohol

Source: Kimi deep-research + Cla

Combined Hormonal Contraceptives
Moderate
Database

Enzyme induction reduces efficacy

Use additional/non-hormonal contraception

Source: Kimi deep-research + Cla

Hyponatraemia Inducing Drugs
Moderate
Database

Additive hyponatraemia

Monitor sodium

Source: Kimi deep-research + Cla

Phenytoin
Moderate
Database

Increased phenytoin levels

Monitor phenytoin level

Source: Kimi deep-research + Cla

Related guidelines

Ask House about Licarbazepine

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: Katzung·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20