Monday, March 4, 2013

Lamotrigine Education Video

Lamotrigine



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Lamotrigine
Systematic (IUPAC) name
6-(2,3-dichlorophenyl)-1,2,4-triazine-3,5-diamine
Clinical data
Trade namesLamictal
AHFS/Drugs.commonograph
MedlinePlusa695007
Pregnancy cat.C (US)
Legal statusPOM (UK) -only (US)
RoutesOral
Pharmacokinetic data
Bioavailability98%
Protein binding55%
MetabolismHepatic (mostly UGT1A4-mediated)
Half-life24–34 hours (healthy adults)
ExcretionRenal
Identifiers
CAS number84057-84-1 YesY
ATC codeN03AX09
PubChemCID 3878
IUPHAR ligand2622
DrugBankDB00555
ChemSpider3741 YesY
UNIIU3H27498KS YesY
KEGGD00354 YesY
ChEBICHEBI:6367 N
ChEMBLCHEMBL741 YesY
Chemical data
FormulaC9H7Cl2N5
Mol. mass256.091 g/mol
N (what is this?) (verify)
Lamotrigine, marketed in the US and most of Europe as Lamictal (pron.: /ləˈmɪktəl/) by GlaxoSmithKline, is an anticonvulsant drug used in the treatment of epilepsy and bipolar disorder. It is also used off-label as an adjunct in treating depression.[1] For epilepsy, it is used to treat focal seizures, primary and secondary tonic-clonic seizures, and seizures associated with Lennox-Gastaut syndrome. Like many other anticonvulsant medications, Lamotrigine also seems to act as an effective mood stabilizer, and has been the first U.S. Food and Drug Administration (FDA)-approved drug for this purpose since lithium, a drug approved almost 30 years earlier. It is approved for the maintenance treatment of bipolar type I. Chemically unrelated to other anticonvulsants (due to lamotrigine's being a phenyltriazine), lamotrigine has many possible side-effects. Lamotrigine is generally accepted to be a member of the sodium channel blocking class of antiepileptic drugs,[2] but it could have additional actions inasmuch as it has a broader spectrum of action than other sodium channel antiepileptic drugs such as phenytoin and carbamazepine and is effective in the treatment of the depressed phase of bipolar disorder, whereas other sodium channel blocking antiepileptic drugs are not. In addition, lamotrigine shares few side-effects with other, unrelated anticonvulsants known to inhibit sodium channels, which further emphasizes its unique properties.[3] Lamotrigine is inactivated by hepatic glucuronidation.

 

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