Oxcarbazepine: Difference between revisions
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==Special Populations== | ==Special Populations== | ||
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: | *[[Drug Ratings in Pregnancy|Pregnancy Rating]]: C | ||
*[[Lactation risk categories|Lactation risk]]: | *[[Lactation risk categories|Lactation risk]]: safety unknown | ||
===Renal Dosing=== | ===Renal Dosing=== | ||
*Adult: CrCl <30: start 150 mg bid; HD/PD: no supplement; Info: titrate dose slowly until response | *Adult: CrCl <30: start 150 mg bid; HD/PD: no supplement; Info: titrate dose slowly until response | ||
*Pediatric: | *Pediatric: CrCl <30: decr. start dose 50%, max start dose 300 mg/24h; HD/PD: no supplement; Info: titrate dose slowly until response | ||
===Hepatic Dosing=== | ===Hepatic Dosing=== | ||
*Adult: mild-mod impairment: no adjustment; severe impairment: not defined | *Adult: mild-mod impairment: no adjustment; severe impairment: not defined | ||
*Pediatric: | *Pediatric: mild-mod impairment: no adjustment; severe impairment: not defined | ||
==Contraindications== | ==Contraindications== | ||
Revision as of 23:42, 10 February 2016
Administration
- Type: anti epileptic
- Dosage Forms: 150,300,600; 300/5 mL
- Routes of Administration: PO
- Common Trade Names: Trileptal
Adult Dosing
Partial seizures
- adjunct tx: Dose: 600 mg PO bid; Start: 300 mg PO bid, incr. by up to 600 mg/day qwk; Max: 2400 mg/day;
- conversion to monotherapy: Dose: 1200 mg PO bid; Start: 300 mg PO bid, incr. by up to 600 mg/day qwk; Max: 2400 mg/day; D/C concomitant anticonvulsants over 3-6wk; taper dose gradually to D/C
- initial monotherapy: Dose: 600 mg PO bid; Start: 300 mg PO bid, incr. by 300 mg/day q3 days; Max: 2400 mg/day
Trigeminal neuralgia
- 450-1200 mg PO bid
- Start: 300 mg PO bid, may incr. by 600 mg/day qwk
Bipolar disorder
- 600-1200 mg PO bid
- Start: 300 mg PO bid, incr. by 300 mg/day q3 days or by 600 mg/day qwk
Pediatric Dosing
Partial seizures
adjunct therapy
- 2-3 yo
- Dose: 60 mg/kg/day PO divided bid; Start: 8-10 mg/kg/day PO divided bid up to 600 mg/day, incr. dose over 2-4wk; Max: 60 mg/kg/day
- may start 16-20 mg/kg/day PO divided bid in pts <20 kg
- 4-16 yo, 20-29 kg
- Dose: 600 mg PO bid; Start: 8-10 mg/kg/day PO divided bid up to 600 mg/day, incr. to target dose over 2wk
- 4-16 yo, >39 kg
- Dose: 900 mg PO bid; Start: 8-10 mg/kg/day PO divided bid up to 600 mg/day, incr. to target dose over 2wk
monotherapy
- 4-16 yo, 20-24 kg
- Dose: 300-450 mg PO bid; Start: 8-10 mg/kg/day PO divided bid, incr. by 5 mg/kg/day q3 days if initial monotherapy or by up to 10 mg/kg/day qwk if conversion to monotherapy
- D/C concomitant anticonvulsants over 3-6wk
- 4-16 yo, 25-34 kg
- Dose: 450-600 mg PO bid; Start: 8-10 mg/kg/day PO divided bid, incr. by 5 mg/kg/day q3 days if initial monotherapy or by up to 10 mg/kg/day qwk if conversion to monotherapy
- D/C concomitant anticonvulsants over 3-6wk
- 4-16 yo, 35-44 kg
- Dose: 450-750 mg PO bid; Start: 8-10 mg/kg/day PO divided bid, incr. by 5 mg/kg/day q3 days if initial monotherapy or by up to 10 mg/kg/day qwk if conversion to monotherapy
- D/C concomitant anticonvulsants over 3-6wk
- 4-16 yo, 45-49 kg
- Dose: 600-750 mg PO bid; Start: 8-10 mg/kg/day PO divided bid, incr. by 5 mg/kg/day q3 days if initial monotherapy or by up to 10 mg/kg/day qwk if conversion to monotherapy
- D/C concomitant anticonvulsants over 3-6wk
- 4-16 yo, 50-59 kg
- Dose: 600-900 mg PO bid; Start: 8-10 mg/kg/day PO divided bid, incr. by 5 mg/kg/day q3 days if initial monotherapy or by up to 10 mg/kg/day qwk if conversion to monotherapy
- D/C concomitant anticonvulsants over 3-6wk
- 4-16 yo, 60-69 kg
- Dose: 600-1050 mg PO bid; Start: 8-10 mg/kg/day PO divided bid, incr. by 5 mg/kg/day q3 days if initial monotherapy or by up to 10 mg/kg/day qwk if conversion to monotherapy
- D/C concomitant anticonvulsants over 3-6wk
- 4-16 yo, >70 kg
- Dose: 750-1050 mg PO bid; Start: 8-10 mg/kg/day PO divided bid, incr. by 5 mg/kg/day q3 days if initial monotherapy or by up to 10 mg/kg/day qwk if conversion to monotherapy
- D/C concomitant anticonvulsants over 3-6wk
Special Populations
- Pregnancy Rating: C
- Lactation risk: safety unknown
Renal Dosing
- Adult: CrCl <30: start 150 mg bid; HD/PD: no supplement; Info: titrate dose slowly until response
- Pediatric: CrCl <30: decr. start dose 50%, max start dose 300 mg/24h; HD/PD: no supplement; Info: titrate dose slowly until response
Hepatic Dosing
- Adult: mild-mod impairment: no adjustment; severe impairment: not defined
- Pediatric: mild-mod impairment: no adjustment; severe impairment: not defined
Contraindications
- Allergy to class/drug
Adverse Reactions
Serious
Common
Pharmacology
- Half-life:
- Metabolism:
- Excretion:
