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  2. Lamotrigine - Wikipedia

    en.wikipedia.org/wiki/Lamotrigine

    Lamotrigine is metabolized predominantly by glucuronic acid conjugation. Its major metabolite is an inactive 2-n-glucuronide conjugate. [82] Lamotrigine has fewer drug interactions than many anticonvulsant drugs, although pharmacokinetic interactions with carbamazepine, phenytoin and other hepatic enzyme-inducing medications may shorten half ...

  3. Felbamate - Wikipedia

    en.wikipedia.org/wiki/Felbamate

    Felbamate interacts with several other AEDs, including phenytoin, valproate, and carbamazepine; dosage adjustments may be necessary to avoid adverse effects. Concomitant administration of felbamate and carbamazepine decreases blood levels of both drugs, while increasing the level of carbamazepine-10,11 epoxide , the active metabolite of ...

  4. Valproate - Wikipedia

    en.wikipedia.org/wiki/Valproate

    Valproate (valproic acid, VPA, sodium valproate, and valproate semisodium forms) are medications primarily used to treat epilepsy and bipolar disorder and prevent migraine headaches. [7] They are useful for the prevention of seizures in those with absence seizures , partial seizures , and generalized seizures . [ 7 ]

  5. Sodium channel blocker - Wikipedia

    en.wikipedia.org/wiki/Sodium_channel_blocker

    Calcium has been shown to block sodium channels [2] which explains the effects of hypercalcemia and hypocalcemia.; Lamotrigine is known to block sodium channels but it is not known whether it is extracellular or intracellular.

  6. Ethosuximide - Wikipedia

    en.wikipedia.org/wiki/Ethosuximide

    Ethosuximide, sold under the brand name Zarontin among others, is a medication used to treat absence seizures. [4] It may be used by itself or with other antiseizure medications such as valproic acid. [4]

  7. Lacosamide - Wikipedia

    en.wikipedia.org/wiki/Lacosamide

    The dose-response curve for lacosamide is linear and proportional for oral doses of up to 800 mg and intravenous doses of up to 300 mg. [32] Lacosamide has low potential for drug-drug interactions, and no pharmacokinetic interactions have been found to occur with other (AEDs) that act on sodium channels. [33]

  8. Oxcarbazepine - Wikipedia

    en.wikipedia.org/wiki/Oxcarbazepine

    Oxcarbazepine, licarbazepine and many other common drugs influence each other through interaction with the cytochrome P450 family of enzymes. This leads to a cluster of dozens of common drugs interacting with one another to varying degrees, some of which are especially noteworthy.

  9. Histone deacetylase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Histone_deacetylase_inhibitor

    The tail suspension test (TST) and the forced swimming test (FST) measure the level of defeat in rodents— usually after treatment with chronic stress— which mirrors symptoms of human depression. Alongside tests for levels of HDAC mRNA, acetylation and gene expression these behavioral tests are compared to controls to determine whether or ...