- Levetiracetam
Chembox new
ImageFileL1 = levetiracetam.png
ImageSizeL1 = 110px
ImageFileR1 = Levetiracetam3d.png
ImageSizeR1 = 110px
ImageFile2 = levetiracetam.gif
ImageSize2 = 121px
IUPACName = (2S)-2-(2-oxopyrrolidin-1-yl)butanamide
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Section1 = Chembox Identifiers
PubChem = 441341
CASNo = 102767-28-2
ATCCode_prefix = N03
ATCCode_suffix = AX14
SMILES = CC [C@@H] (C(=O)N)N1CCCC1=O
Section2 = Chembox Properties
Formula = | C=8 | H=14 | N=2 | O=2
MolarMass = 170.209 g/mol
Appearance = Fine white crystalline powder
Density =
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Section5 = Chembox Pharmacology
AdminRoutes = Oral, Intravenous
Bioavail = ~100%
Metabolism =
HalfLife = 6 - 8 hr
ProteinBound =
Excretion = Urinary
Legal_status =
Legal_US = POM
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PregCat_US = CLevetiracetam (INN) (pronEng|lɛvɨtɪˈræsɨtæm) is an
anticonvulsant medication used to treatepilepsy . It is "S"-enantiomer ofetiracetam , structurally similar to the prototypicalnootropic drugpiracetam . Along with other anticonvulsants likegabapentin , it is also sometimes used to treat neuropathic pain. Levetiracetam is marketed under the trade name Keppra. Keppra is manufactured by UCB Pharmaceuticals Inc.Levetiracetam has recently been approved in the United Kingdom as a
monotherapy treatment for epilepsy. It is also used in veterinary medicine for similar purposes.Mechanism
Levetiracetam binds to a synaptic vesicle protein, SV2A.cite journal | last=Lynch | first=BA | coauthors= Lambeng N, Nocka K | title=The synaptic vesicle protein SV2A is the binding site for the antiepileptic drug levetiracetam | journal=Proceedings of the National Academy of Sciences of the United States of America | volume=101 | issue=26 | pages=9861–9866 | publisher=The National Academy of Sciences | date=June 2004 | url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=15210974 | pmid=15210974 | doi=10.1073/pnas.0308208101 | accessdate=2008-07-21 ] This is believed to impede nerve conduction across synapses.cite journal | last=Rogawski | first=MA | title=Diverse mechanisms of antiepileptic drugs in the development pipeline | journal=Epilepsy Research | volume=69 | issue=3 | pages=273–294 | publisher=National Institutes of Health | date=June 2006 | url=http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=16621450 | pmid=16621450 | doi=10.1016/j.eplepsyres.2006.02.004 | accessdate=2008-07-21 ]
Side effects
Side effects include:
hair loss ;pins and needles sensation in the extremities; psychiatric symptoms ranging fromirritability to depression; and other common side effects likeheadache andnausea . Recent literature [http://www.aesnet.org/Visitors/AnnualMeeting/Abstracts/dsp_Abstract.cfm?id=3367] (and paper 2.163 in [http://www.blackwell-synergy.com/doi/abs/10.1111/j.1528-1167.2005.460801_16.x] ) suggests that the addition ofpyridoxine (vitamin B6) may curtail some of the psychiatric symptoms.Levetiracetam is generally well tolerated but may cause sleepiness, weakness, dizziness, and infection. In children, the most common side effects are sleepiness, accidental injury, hostility, irritability, and weakness. [http://www.keppra.com/pc/home/default.asp]
References
* [http://www.fda.gov/cder/foi/label/1999/21035lbl.pdf Keppra (levetiracetam) Final Printed Label] New and Generic Drug Approvals. 29 Dec 1999. Center for Drug Evaluation and Research, U.S. Food and Drug Administration. Accessed 31 August 2005.
*External links
* [http://www.keppra.com/ Keppra UCB] (manufacturer's website)
* [http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a699059.html NIH MedLine drug information]ee also
*
Racetams
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