Felbamate ' s chemical structure
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Felbamate

Felbamate (marketed as Felbamol by MedPointe) is an anticonvulsant drug used in the treatment of epilepsy. It is used to treat partial seizures (with and without generalization) in adults and partial and generalized seizures associated with Lennox-Gastaut syndrome in children. However, an increased risk of potentially fatal aplastic anemia and/or liver failure limit the drugs usage to severe refractory epilepsy. more...

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Mechanism of Action

As with most anticonvulsants, the precise mechanism is unknown. It has a weak inhibitory effect on GABA receptor binding sites.

Approval History

U.S.

  • August 1993. Felbamate was approved for partial seizures with and without secondary generalization in adults and for Lennox-Gastaut Syndrome, a serious form of childhood epilepsy. Over the following year 150,000 people were started on felbamate therapy and a third of these became established.
  • August 1st 1994. It was urgently withdrawn after 10 cases of aplastic anemia. A "Dear Doctor" letter was sent to 240,000 physicians.
  • September 27th 1994. Felbamate had a limited redemption in another "Dear Doctor" letter sent to 260,000 physicians. It was recommended that the drug remain available only for patients with severe epilepsy for whom the benefits outweigh the risks, and that changes be made to the product's labelling to reflect the newly recognized risk . This redemption came with an additional warning since there had been 10 cases acute liver failure (4 of which were fatal). At this point, 10,000 to 12,000 people remained on the drug.

U.K.

  • The drug is only available on a limited named-patient basis.

Indications & Usage

  • Adults: Monotherapy or adjunctive therapy in the treatment of partial seizures, with and without generalization.
  • Children: Adjunctive therapy in the treatment of partial and generalized seizures associated with Lennox-Gastaut syndrome.

Dosing

Felbamate is available in tablets (400 mg and 600 mg) and as a peach-coloured oral suspension (600 mg/5 mL).

  • Adults (> 14 years): begin with 1,200 mg daily given every 6 to 8 hours
  • Children (2 > 14 years): 15 to 45 mg per kg per day given every 6 to 8 hours

Side Effects

Adverse reactions include decreased appetite, vomiting, insomnia, nausea, dizziness, somnolence, and headache. Many patients report increased alertness with the drug. Two rare but very serious effects include aplastic anemia and hepatic (liver) failure. The risk of aplastic anemia is between 1:3,600 and 1:5,000, of which 30% of cases are fatal. The risk of hepatic failure is between 1:24,000 to 1:34,000.

Drug Interactions

Felbamate interacts with other AEDs, the dose of which may be reduced in order to avoid adverse effects.

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Newer Medications for Pediatric Epilepsy
From American Family Physician, 5/1/00 by Grace Brooke Huffman

Up to one quarter of children diagnosed with epilepsy are refractory to treatment with traditional antiepileptic drugs (AEDs). Once appropriate classification of the seizure disorder has been accomplished, an AED should be selected based on efficacy, side effect profile and pharmacokinetic characteristics. Unfortunately, there is a lack of controlled trials on the use of AEDs in children, and most agents have been labeled by the U.S. Food and Drug Administration (FDA) for use in adults only. Pellock reviews the current understanding of management of pediatric epilepsy with newer AEDs.

In 1993, felbamate was labeled for adjunctive treatment of partial and generalized seizures in children with Lennox-Gastaut syndrome. There were numerous reports of hepatotoxicity and aplastic anemia in adults, but there have been no reports of aplastic anemia in children younger than 13 years. Felbamate is therefore a treatment option in children whose seizures are not controlled with traditional AEDs. It proved to be highly beneficial in a study of children older than 10 years, who had a more than 50 percent reduction in the frequency of seizures while taking felbamate. Major side effects include aplastic anemia (possibly at a rate of one case per 8,000), anorexia, somnolence, nausea and vomiting, and gait abnormalities. An initial adjunctive dosage is 15 to 45 mg per kg per day, but much higher dosages may be needed. The author recommends that this drug be taken only in consultation with a pediatric neurologist.

Gabapentin is labeled by the FDA for adjunctive treatment of partial and secondarily generalized seizures in adults. It can be titrated quickly and easily, and its adverse effects (e.g., behavioral changes and aggression) are mild. Gabapentin's efficacy in children seems to be dosage-dependent. Initial dosage recommendations are 10 to 20 mg per kg per day, increasing to 30 mg per kg per day. Some children may need dosages as high as 60 to 100 mg per kg per day. One study showed particularly good response in mentally retarded children who had resistant partial epilepsy.

Lamotrigine is given to children in dosages ranging from 1 to 15 mg per kg per day. Careful dosing attention is needed because adverse effects are much more common at higher dosages. Serious rashes have been reported in up to 12 percent of patients, often in children who are also taking valproate and whose dosage is titrated rapidly. The rash may progress to Stevens-Johnson syndrome or toxic epidermal necrolysis. Lamotrigine seems to be especially useful in children with Lennox-Gastaut syndrome, generalized epilepsy syndromes and refractory partial epilepsy.

Tiagabine is labeled for adjunctive treatment of partial seizures. Although higher dosages (up to 56 mg per day) seem to be most effective, dosing starts in children at 0.1 mg per kg per day. As with most newer AEDs, data in children are limited, but this medication seems to be effective in children with partial seizures. Tiagabine selectively inhibits the uptake of g-aminobutyric acid and, as such, might be useful in the treatment of infantile spasms. Further studies are needed. Side effects include headache, dizziness and somnolence. Topiramate may be useful as adjunctive and monotherapy in children with refractory partial seizures. The initial dosage is 1 mg per kg per day, with titration up to 6 mg per kg per day. Major side effects include somnolence, dizziness, psychomotor slowing, paresthesias and confusion. Some adult patients have also developed nephrolithiasis and weight loss.

One investigational medication, vigabatrin, has been shown to be quite effective in a number of pediatric epilepsies, especially infantile spasms. It has also been used successfully in children with Lennox-Gastaut syndrome but may exacerbate myoclonic seizures.

The author concludes that first-line treatment of pediatric epilepsy should still involve the use of conventional AEDs. However, the newer AEDs offer more options, especially in children with refractory seizures. The accompanying table summarizes treatment guidelines for new antiepileptic drugs.

Pellock JM. Managing pediatric epilepsy syndromes with new antiepileptic drugs. Pediatrics November 1999; 104:1106-16.

COPYRIGHT 2000 American Academy of Family Physicians
COPYRIGHT 2000 Gale Group

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