TEGRETOL-XR
What it isExtended-release sodium-channel-blocking antiepileptic; seizures and trigeminal neuralgia.
Why this oneBID dosing with flatter peaks than IR reduces peak-related dizziness and diplopia; shell may appear in stool, and Carbatrol ER capsules are the sprinklable sibling.
What limits itSerious HLA-associated rash and marrow failure are boxed risks; autoinduction, drug interactions, and hyponatremia complicate use.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Epilepsy (partial/complex, generalized tonic-clonic, mixed seizures) | >12 yr and adults | 200 mg BID (400 mg/day) | Increase 200 mg/day weekly; maintenance usually 800–1200 mg/day | 1000 mg/day (12–15 yr); 1200 mg/day (>15 yr); 1600 mg/day (adults, rare) |
| Epilepsy | Children 6–12 yr | 100 mg BID (200 mg/day) | Increase 100 mg/day weekly; maintenance usually 400–800 mg/day | 1000 mg/day |
| Epilepsy | Children <6 yr | 10–20 mg/kg/day divided BID–TID (tablet/suspension) | Increase weekly; maintenance usually <35 mg/kg/day | 35 mg/kg/day |
| Trigeminal neuralgia | Adults | 100 mg BID (200 mg/day) | Increase up to 200 mg/day; maintenance 400–800 mg/day | 1200 mg/day |
Titration Increase at weekly intervals (epilepsy); trigeminal neuralgia by up to 200 mg/day.
Renal Prescribe only after critical benefit-to-risk appraisal in patients with renal damage.
Hepatic Prescribe only after critical benefit-to-risk appraisal in hepatic damage; hepatic effects up to hepatic failure reported.
Pregnancy Can cause fetal harm (spina bifida, craniofacial/cardiovascular defects, developmental delay).
Lactation Undefined.
⚠ BOXED WARNINGS

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