Antidote:: MDAC, +/- haemodialysis
- structurally related to [[TCA overdose|TCAs]] and phenytoin ; similar pattern of toxicity
- [[Sodium channel blocker|Na-channel blocker]]
- [[Anticholinergic toxicity|antimuscarinic]] actions
**Risk assessment**
- peak plasma concentrations after 8-12 hours for toxic ingestions of immediate release formulations ; 24-96 hours of slow release formulations in massive OD
- small Vd 1L/kg
- therapeutic range 20-50 micromol/L
- moderate tox is 80-160 micromol/L
- profound ↓ GCS
- frequent dystoic reactions
- tachycardia
- severe tox > 180 micromol/L
- [[Seizures#Toxicological Seizures]]
- GCS 3
- hypotension and myocardial depression common
- QRS widening, [[Long QT|QTc]] prolongation, arrhythmias
- **children**
- toxicity at levels 30% lower than adults due to ↑ active metabolite production
- higher incidence of dystonia, choreoathetosis and seizures
- lower incidence of cardiotoxicity
| severity | dose ingested <br>mg/kg | concentration <br>umol/L (mg/L) |
| --------- | ----------------------- | ------------------------------- |
| mild/none | <20 | ≤ 85 ( ≤20) |
| moderate | 20-50 | 85-170 (20 - 40) |
| severe | >50 | >170 (>40) |
**Management**
- decontamination -- [[Decontamination#Dose for MDAC|MDAC]] in significant toxicity
- hypotension -- IVF
- [[HCO3 therapy|NaHCO3]] if:
- fluid-resistant
- QRS widening
- significant arrhythmias
- add adrenaline or noradrenaline if fluid resistant
- seizures -- benzos
- [[haemodialysis]]
- severe toxicity resistant to non-invasive therapy
- *haemofiltration* is method of choice in severe toxicity as it also removes protein bound drug
- *haemodialysis* effective in removing CVZ-E
- charcoal haemoperfusion decreases toxic levels by 20%, however this is the same as MDAC.
# Related Questions
## carbamazepine
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