Sodium valproate

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Main article: Valproic acid
Sodium valproate
Systematic (IUPAC) name
sodium 2-propylpentanoate
Identifiers
CAS number 1069-66-5
ATC code N03AG01
PubChem 14047
Chemical data
Formula C8H15NaO2 
Mol. mass 166.20 g/mol
Pharmacokinetic data
Bioavailability  ?
Protein binding 90–95%
Metabolism 75% by CYP enzymes
Half life 9–18 hours
Excretion 20% excreted as glucuronide
Therapeutic considerations
Pregnancy cat.

D(AU) D(US)

Legal status

POM(UK) -only(US)

Routes Oral, i.v.

Sodium valproate (INN) or valproate sodium (USAN) is the sodium salt of valproic acid and is an anticonvulsant used in the treatment of epilepsy and bipolar disorder, as well as other psychiatric conditions requiring the administration of a mood stabilizer. The intravenous formulations are used when oral administration is not possible.

Contents

[edit] Formulations

Trade names are in bold, followed by the manufacturer.

[edit] U.S.

[edit] UK and Australia

  • Tablets – Orlept by Wockhardt and Epilim by Sanofi-Aventis.
  • Oral solution – Orlept Sugar Free by Wockhardt and Epilim by Sanofi-Aventis.
  • Syrup – Epilim by Sanofi-Aventis.
  • Intravenous injection – Epilim Intravenous by Sanofi-Aventis.
  • Extended release tablets – Epilim Chrono by Sanofi-Aventis. A combination of sodium valproate and valproic acid in a 2.3:1 ratio.
  • Enteric-coated tablets – Epilim EC200 by Sanofi-synthélabo. A 200 mg sodium valproate enteric-coated tablet.

[edit] Germany, Switzerland, Norway

  • Tablets – Orfiril by Desitin Pharmaceuticals
  • Intravenous injection – Orfiril IV by Desitin Pharmaceuticals

[edit] South Africa

  • Syrup – Convulex by Byk Madaus
  • Tablets – Epilim by sanofi~synthelabo

[edit] Canada

[edit] Japan

  • Tablets – Depakene by Kyowa Hakko Kogyo.
  • Extended release tablets – Depakene-R by Kyowa Hakko Kogyo and Selenica-R by Kowa.
  • Syrup – Depakene by Kyowa Hakko Kogyo.

[edit] Others

In much of Europe, Depakine and Depakine Chrono are equivalent to Epilim and Epilim Chrono above.

[edit] Safety in pregnancy

All antiepilepic medications have been shown to be associated with higher risks of fetal abnormalities (mostly for spina bifida) since at least 1983 with the risks being related to the strength of medication used and use of more than one drug.[1][2] Valproate has also been recognised as sometimes causing a specific facial changes ("facial phenotype") termed "fetal valproate syndrome".[3] Sodium valproate has been associated with the rare condition Paroxysmal tonic upgaze of childhood from childhood exposure(Epileptic Disord. 2007 Sep;9(3):332-6) and also fetal exposure (This condition resolved after discontinuing valproate therapy. Ouvrier-Billson syndrome (J Child Neurol. 1988 Jul;3(3):177-80) is the name used for this condition, to honor the discoverer.

Whilst developmental delay is usually associated with altered physical characterists (dysmorphic features), this may occur on its own.[4]

A 2005 study found rates of autism among children exposed to sodium valproate before birth in the cohort studied were 8.9%.[5] The normal incidence for autism in the general population is estimated at less than one percent.[6] It has been suggested that Valproate may best be avoided in women with localisation epilepsy, where there are more effective and less risky alternatives such as carbamazepine.[4]

A class action is currently underway in the United Kingdom regarding the claim that the drug used in pregnancy caused a range of problems in children, including autism, learning and social difficulties, ADHD, spinal stenosis, facial abnormalities, vision defects, dyslexia, dyspraxia, delayed speech and motor development.[7][unreliable source?]

[edit] See also

[edit] References

  1. ^ Koch S, Göpfert-Geyer I, Jäger-Roman E, et al (February 1983). "[Anti-epileptic agents during pregnancy. A prospective study on the course of pregnancy, malformations and child development]" (in German). Dtsch. Med. Wochenschr. 108 (7): 250–7. PMID 6402356. 
  2. ^ Moore SJ, Turnpenny P, Quinn A, et al (July 2000). "A clinical study of 57 children with fetal anticonvulsant syndromes". J. Med. Genet. 37 (7): 489–97. PMID 10882750. 
  3. ^ DiLiberti JH, Farndon PA, Dennis NR, Curry CJ (November 1984). "The fetal valproate syndrome". Am. J. Med. Genet. 19 (3): 473–81. doi:10.1002/ajmg.1320190308. PMID 6439041. 
  4. ^ a b Adab N, Kini U, Vinten J, et al (November 2004). "The longer term outcome of children born to mothers with epilepsy". J. Neurol. Neurosurg. Psychiatr. 75 (11): 1575–83. doi:10.1136/jnnp.2003.029132. PMID 15491979. “This argues that the fetal valproate syndrome constitutes a real clinical entity that includes developmental delay and cognitive impairments, but that some children might exhibit some developmental delay without marked dysmorphism.” 
  5. ^ Rasalam AD, Hailey H, Williams JH, et al (August 2005). "Characteristics of fetal anticonvulsant syndrome associated autistic disorder". Dev Med Child Neurol 47 (8): 551–5. PMID 16108456. 
  6. ^ http://www.autism-society.org/site/PageServer?pagename=about_home
  7. ^ http://www.irwinmitchell.com/PressOffice/PressReleases/epilepsy-drug-claims.htm

[edit] External links

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