Rufinamide (rufinamide)

Anticonvulsants Oral Suspension, Oral (Final Dose Form); Oral Tablet

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Rufinamide is a triazole-derivative anticonvulsant.

Rufinamide, a triazole derivative, is an anticonvulsant agent that is structurally unrelated to other currently available anticonvulsants. Although the precise mechanism(s) of anticonvulsant action of rufinamide is unknown, results of in vitro studies suggest that the principal mechanism is modulation of sodium channel activity and, in particular, prolongation of the inactive state of the channel. Rufinamide does not appear to substantially interact with monoaminergic, cholinergic, histaminergic, glycine, gamma-aminobutyric acid (GABA), or glutamate receptors or systems.

Rufinamide is extensively metabolized but has no active metabolites; the primary form of biotransformation is via carboxylesterase-mediated hydrolysis of the carboxylamide group to the acid derivative CGP 47292. Cytochrome P-450 (CYP) isoenzymes and glutathione do not appear to be involved in the drug's metabolism. At clinically relevant concentrations, rufinamide demonstrates little or no inhibition of most CYP isoenzymes; however, the drug is a weak inhibitor of CYP2E1 and a weak inducer of CYP3A4.

Following administration of a radiolabeled dose, less than 2% of the dose was recovered in the urine as unchanged drug. The majority of rufinamide (85% of a radiolabeled dose) is eliminated renally. Rufinamide exhibits a low degree of protein binding (34%), principally to albumin (27%), and has a mean elimination half-life of approximately 6-10 hours.

USES: Rufinamide is used to treat seizures associated with Lennox-Gastaut syndrome (LGS).

Generic name: rufinamide
Pronunciation: (roo-FIN-a-mide)
Drug class: Anticonvulsants
Therapeutic class: Central Nervous System Agents

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Rufinamide:

  • Lennox-Gastaut Epilepsy

Also known as: Epilepsy Of Lennox Gastaut Syndrome.

Dosing

For the adjunctive management of seizures associated with Lennox-Gastaut syndrome in children and adolescents 1 to less than 17 years of age, rufinamide therapy should be initiated at a dosage of approximately 10 mg/kg daily administered in 2 equally divided doses. Dosage should be increased in increments of approximately 10 mg/kg every other day up to a maximum dosage of 45 mg/kg (not to exceed 3.2 g) daily, administered in 2 equally divided doses. The manufacturer states that the efficacy of dosages lower than the target dosage has not been established.

For the adjunctive management of seizures associated with Lennox-Gastaut syndrome in adults 17 years of age and older, rufinamide therapy should be initiated at a dosage of 400-800 mg daily administered in 2 equally divided doses. Dosage should be increased in increments of 400-800 mg every other day until a maximum daily dosage of 3.2 g, administered in 2 equally divided doses, is reached. The manufacturer states that the efficacy of dosages lower than 3.2 g daily has not been established.

The target dosage was achieved in 88% of rufinamide-treated patients with Lennox-Gastaut syndrome in the principal efficacy study; the majority of these patients reached the target dosage within 7 days, with the remaining patients achieving the target dosage within 14 days.

Valproic acid may increase plasma concentrations of rufinamide by up to 70% during concurrent use. Patients who are stabilized on rufinamide therapy should initiate valproic acid therapy at a low dosage; dosage of valproic acid should then be titrated to a clinically effective dosage. Patients already receiving valproic acid therapy should begin rufinamide therapy at a dosage lower than 10 mg/kg daily (in children) or a dosage lower than 400 mg daily (in adults).

Drug interactions

In vitro and in vivo studies have demonstrated that rufinamide is unlikely to be involved in clinically important pharmacokinetic interactions.

Contraindications

Patients with familial short QT syndrome. (See Shortening of QT Interval under Cautions: Warnings/Precautions.)

Adverse reactions

Adverse effects occurring in 3% or more of pediatric patients and more frequently than with placebo in controlled studies in which rufinamide was administered in conjunction with other anticonvulsants include somnolence, headache, fatigue, dizziness, influenza, nasopharyngitis, nausea, vomiting, constipation, stomach pain, decreased appetite, decreased weight, cough, sinusitis, bronchitis, pneumonia, otitis media, rash, pruritus, ataxia, diplopia, aggression, hyperactivity, and disturbance in attention.

Adverse effects occurring in 3% or more of adults and more frequently than with placebo in controlled studies in which rufinamide was administered in conjunction with other anticonvulsants include headache, dizziness, fatigue, somnolence, diplopia, tremor, nystagmus, blurred vision, nausea, vomiting, stomach pain, constipation, dyspepsia, ataxia, anxiety, back pain, gait disturbance, and vertigo.

Precautions

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ICD codes

CodeTypeDescription
Lennox-gastaut epilepsy
G40.81ICD10CMLennox-gastaut syndrome
G40.812ICD10CMLennox-gastaut syndrome, not intractable, without status epilepticus
G40.814ICD10CMLennox-gastaut syndrome, intractable, without status epilepticus

ICD code information from First Databank (FDB).

Formulary status

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Last reviewed · Source: First Databank (FDB) drug data