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Indications

BEERS REMS

Equetro only:

Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Exercise Extreme Caution in:

Adv. Reactions/Side Effects

CV: HF, edema, heart block, hypertension, hypotension, syncope.

Derm: DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS (DRESS), nail shedding, photosensitivity, rash, STEVENS-JOHNSON SYNDROME, TOXIC EPIDERMAL NECROLYSIS, urticaria.

EENT: blurred vision, corneal opacities, nystagmus.

Endo: SIADH.

F and E: hyponatremia.

GI: ↑ liver enzymes, HEPATOTOXICITY, PANCREATITIS.

GU: hesitancy, urinary retention.

Hemat: AGRANULOCYTOSIS, APLASTIC ANEMIA, eosinophilia, leukopenia, lymphadenopathy, THROMBOCYTOPENIA.

Metab: weight gain.

Neuro: ataxia, drowsiness, fatigue, psychosis, sedation, SUICIDAL THOUGHTS, vertigo.

Resp: pneumonitis.

Misc: chills, fever.

Interactions

Drug-Drug:

Drug-Food:

Availability

(Generic available)

Route/Dosage

see Calculator

When converting from immediate-release to extended-release formulation, administer same total daily dose (in 2 divided doses).

Seizures

Trigeminal Neuralgia

Acute Manic or Mixed Episodes Associated with Bipolar I Disorder

US Brand Names

Carbatrol, Epitol, Equetro, TEGretol, TEGretol XR

Action

Therapeutic Effects:

Classifications

Therapeutic Classification: anticonvulsants

Pharmacokinetics

Absorption: Absorption is slow but complete. Suspension produces earlier, higher peak, and lower trough levels.

Distribution: Widely distributed. Crosses the blood-brain barrier. Crosses the placenta rapidly and enters breast milk in high concentrations.

Protein Binding: Carbamazepine: 75–90%; epoxide: 50%.

Metabolism/Excretion: Extensively metabolized in the liver by the CYP3A4 isoenzyme to active epoxide metabolite; epoxide metabolite has anticonvulsant and antineuralgic activity.

Half-life: Carbamazepine: single dose—25–65 hr, chronic dosing—Children: 8–14 hr; Adults: 12–17 hr; epoxide: 34±9 hr.

Canadian Brand Names

TEGretol CR

Time/Action Profile

(anticonvulsant activity)

ROUTEONSETPEAKDURATION
POup to 1 mo†4–5 hr‡6–12 hr
PO-ERup to 1 mo†2–3–12 hr‡12 hr

†Onset of antineuralgic activity is 8–72 hr.

‡Listed for tablets; peak level occurs 1.5 hr after a chronic dose of suspension.

Patient/Family Teaching

Pronunciation

kar-ba-MAZ-e-peen audio

Code

NDC Code*