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Valproate ( VPA ), and its valproic acid, sodium valproate, and valproate semisodium forms, are medications primarily used to treat epilepsy and bipolar disorder and to prevent migraine headaches.
Common side effects include nausea, vomiting, sleepiness, and a dry mouth.
It is unclear exactly how valproate works.
Valproate was first made in 1881 and came into medical use in 1962.
1 Terminology
2 Medical uses
2.1 Epilepsy
2.2 Mental illness
2.2.1 Bipolar disorder
2.2.2 Schizophrenia
2.2.3 Dopamine dysregulation syndrome
2.3 Migraines
2.4 Other
3 Adverse effects
3.1 Other possible side effects
3.2 Pregnancy
3.3 Elderly
3.4 Contraindications
3.5 Interactions
3.6 Overdose and toxicity
4 Pharmacology
4.1 Pharmacodynamics
4.1.1 Endocrine actions
4.2 Pharmacokinetics
4.2.1 Metabolism
5 Chemistry
6 History
7 Society and culture
7.1 Cost
7.2 Approval status
7.3 Off-label uses
7.4 Formulations
7.4.1 Brand names of valproic acid
7.4.2 Brand names of sodium valproate Portugal United States Australia New Zealand UK UK only Germany, Switzerland, Norway, Finland, Sweden South Africa Malaysia Romania Canada Japan Europe Taiwan Iran Israel India, Russia and CIS countries
7.4.3 Brand names of valproate semisodium
8 References
9 Further reading
10 External links
Valproic acid (VPA) is an organic weak acid. The conjugate base is valproate. The sodium salt of the acid is sodium valproate and a coordination complex of the two is known as valproate semisodium.
Medical uses
It is used primarily to treat epilepsy and bipolar disorder. It is also used to prevent migraine headaches.
Valproate has a broad spectrum of anticonvulsant activity, although it is primarily used as a first-line treatment for tonic-clonic seizures, absence seizures and myoclonic seizures and as a second-line treatment for partial seizures and infantile spasms.
Mental illness
Bipolar disorder
Valproate products are also used to treat manic or mixed episodes of bipolar disorder.
A 2016 systematic review compared the efficacy of valproate as an add-on for people with schizophrenia :
There is limited evidence that the augmentation of antipsychotics with valproate may be effective for overall response and also for specific symptoms, especially in terms of excitement and aggression. Evidence was entirely based on open randomized controlled trials. Valproate was associated with a number of adverse events among which sedation and dizziness appeared significantly more frequently than in the control groups.
Findings in words
Findings in numbers
Quality of evidence
Global outcome
Clinically significant response
When added to antipsychotic drugs valproate probably increases the chance of improvement. Data are based on moderate quality evidence.
RR 1.31 (1.16 to 1.47)
Leaving the study early for any reason
Valproate in combination with antipsychotics may slightly reduces the chance of leaving the study early, but the difference between the two treatments is not clear. Data supporting this finding are based on moderate quality evidence.
RR 0.76 (0.47 to 1.24)
Use of additional medication for sedation
The combination of valproate and antipsychotic drugs may increase the chance of being given additional sedating medication, but, at present it is not possible to be confident about the difference between the two treatments and data supporting this finding are very limited.
RR 3.65 (0.11 to 122.31)
Very low
Mental state
Average score ( PANSS total, high = poor)
On average, people receiving the valproate combination scored lower (better) than people treated with antipsychotics in combination with placebo or antipsychotic drugs alone. There was a clear difference between the groups, but, the meaning of this in day-to-day care is unclear.
MD 5.85 lower (7.8 lower to 3.91 lower)
Adverse events
Abnormal liver function (blood test changes)*
Adding valproate to antipsychotic drug treatment does not clearly cause liver problems. Data supporting this finding are based on moderate quality evidence.
RR 1.26 (0.72 to 2.22)
Adding valproate to antipsychotic drugs probably causes little or no increase to the chance of feeling sick, but the difference between the two treatments is not clear. Data supporting this finding are based on moderate quality evidence.
RR 1.22 (0.80 to 1.86)
Missing outcomes and notes
Quality of life outcomes were not reported in the included studies. *Increase in alanine transaminase/gamma-glutamyl transpeptidase
Dopamine dysregulation syndrome
Based upon five case reports, valproic acid may have efficacy in controlling the symptoms of the dopamine dysregulation syndrome that arise from the treatment of Parkinson’s disease with levodopa.
Valproate is also used to prevent migraine headaches. Because this medication can be potentially harmful to the fetus, valproate should be considered for those able to become pregnant only after the risks have been discussed.
The medication has been tested in the treatment of AIDS and cancer, owing to its histone deacetylase-inhibiting effects.
Adverse effects
See also: List of adverse effects of valproic acid and List of adverse effects of valproate semisodium
Most common adverse effects include:
Nausea (22%)
Drowsiness (19%)
Dizziness (12%)
Vomiting (12%)
Weakness (10%)
Serious adverse effects include:
Low blood platelets
Suicidal behavior and thoughts
Low body temperature
Valproic acid has a black box warning for hepatotoxicity, pancreatitis, and fetal abnormalities.
Other possible side effects
There is evidence that valproic acid may cause premature growth plate ossification in children and adolescents, resulting in decreased height.
Valproate causes birth defects;
Children of mothers taking valproate during pregnancy are at risk for lower IQs.
Sodium valproate has been associated with the rare condition paroxysmal tonic upgaze of childhood, also known as Ouvrier–Billson syndrome, from childhood or fetal exposure. This condition resolved after discontinuing valproate therapy.
Women who intend to become pregnant should switch to a different medication if possible, or decrease their dose of valproate.
Valproate in elderly people with dementia caused increased sleepiness. More people stopped the medication for this reason. Additional side effects of weight loss and decreased food intake was also associated in one half of people who become sleepy.
Contraindications include:
Pre-existing acute or chronic liver dysfunction or family history of severe liver inflammation (hepatitis), particularly medicine related.
Known hypersensitivity to valproate or any of the ingredients used in the preparation
Urea cycle disorders
Hepatic porphyria
Mitochondrial disease
Valproate inhibits CYP2C9, glucuronyl transferase, and epoxide hydrolase and is highly protein bound and hence may interact with drugs that are substrates for any of these enzymes or are highly protein bound themselves.
Aspirin : may increase valproate concentrations. May also interfere with valproate’s metabolism.
Benzodiazepines : may cause CNS depression and there are possible pharmacokinetic interactions.
Carbapenem antibiotics: reduces valproate levels, potentially leading to seizures.
Cimetidine : inhibits valproate’s metabolism in the liver, leading to increased valproate concentrations.
Erythromycin : inhibits valproate’s metabolism in the liver, leading to increased valproate concentrations.
Ethosuximide : may increase ethosuximide concentrations and lead to toxicity.
Felbamate : may increase plasma concentrations of valproate.
Mefloquine : may increase valproate metabolism combined with the direct epileptogenic effects of mefloquine.
Oral contraceptives : may reduce plasma concentrations of valproate.
Primidone : may accelerate metabolism of valproate, leading to a decline of serum levels and potential breakthrough seizure.
Rifampin : increases the clearance of valproate, leading to decreased valproate concentrations
Warfarin : may increase warfarin concentration and prolong bleeding time.
Zidovudine : may increase zidovudine serum concentration and lead to toxicity.
Overdose and toxicity
Therapeutic range of valproic acid
Lower limit
Upper limit
Total (including protein bound )
µg/mL or mg/l
µg/mL or mg/l
Excessive amounts of valproic acid can result in sleepiness, tremor, stupor, respiratory depression, coma, metabolic acidosis, and death. In general, serum or plasma valproic acid concentrations are in a range of 20–100 mg/l during controlled therapy, but may reach 150–1500 mg/l following acute poisoning. Monitoring of the serum level is often accomplished using commercial immunoassay techniques, although some laboratories employ gas or liquid chromatography.
In contrast to other antiepileptic drugs, at present there is little favorable evidence for salivary therapeutic drug monitoring. Salivary levels of valproic acid correlate poorly with serum levels, partly due to valproate’s weak acid property (p K a of 4.9).
In severe intoxication, hemoperfusion or hemofiltration can be an effective means of hastening elimination of the drug from the body. than L -carnitine.
Although the mechanism of action of valproate is not fully understood,
Prevention of neurotransmitter-induced hyperexcitability of nerve cells, via Kv7.2 channel and AKAP5, may also contribute to its mechanism.
It also has histone deacetylase-inhibiting effects. The inhibition of histone deacetylase, by promoting more transcriptionally active chromatin structures, likely presents the epigenetic mechanism for regulation of many of the neuroprotective effects attributed to valproic acid. Intermediate molecules mediating these effects include VEGF, BDNF, and GDNF.
Endocrine actions
Valproic acid has been found to be an antagonist of the androgen and progesterone receptors, and hence as a nonsteroidal antiandrogen and antiprogestogen, at concentrations much lower than therapeutic serum levels.
Valproic acid has been found to directly stimulate androgen biosynthesis in the gonads via inhibition of histone deacetylases and has been associated with hyperandrogenism in women and increased 4-androstenedione levels in men.
This section needs expansion. You can help by adding to it. (August 2017)
The vast majority of valproate metabolism occurs in the liver.
Valproate is known to be metabolized by the Cytochrome P450 enzymes : CYP2A6, CYP2B6, CYP2C9, and CYP3A5.
Valproic acid is a branched short-chain fatty acid and a derivative of valeric acid.
Valproic acid was first synthesized in 1882 by Beverly S. Burton as an analogue of valeric acid, found naturally in valerian.
Society and culture
It is available as a generic medication.
Approval status
FDA -labelled indication?
TGA -labelled indication?
MHRA -labelled indication?
Literature support
Limited (depends on the seizure type; it can help with certain kinds of seizures: drug-resistant epilepsy, partial and absence seizures, can be used against glioblastoma and other tumors both to improve survival and treat seizures, and against tonic-clonic seizures and status epilepticus).
Bipolar mania
Bipolar depression
Bipolar maintenance
Migraine prophylaxis
Yes (accepted)
Acute migraine management
Only negative results.
Weak evidence.
Agitation in dementia
Weak evidence. Not recommended for agitation in people with dementia.
Fragile X syndrome
Yes (orphan)
Familial adenomatous polyposis
Yes (orphan)
Chronic pain & fibromyalgia
Alcohol hallucinosis
One randomised double-blind placebo-controlled trial.
Intractable hiccups
Limited, five case reports support its efficacy, however.
Non-epileptic myoclonus
Limited, three case reports support its efficacy, however.
Cluster headaches
Limited, two case reports support its efficacy.
West syndrome
A prospective clinical trial supported its efficacy in treating infantile spasms.
HIV infection eradication
Double-blind placebo-controlled trials have been negative.
Myelodysplastic syndrome
Several clinical trials have confirmed its efficacy as a monotherapy,
Acute myeloid leukaemia
Two clinical trials have confirmed its efficacy in this indication as both a monotherapy and as an adjunct to tretinoin.
Cervical cancer
One clinical trial supports its use here.
Malignant melanoma
One phase II study has seemed to discount its efficacy.
Breast cancer
A phase II study has supported its efficacy.
Impulse control disorder
Off-label uses
In 2012, pharmaceutical company Abbott paid $1.6 billion in fines to federal and state governments for illegal promotion of off-label uses for Depakote, including the sedation of elderly nursing home residents.
Sodium valproate Identifiers
IUPAC name
sodium 2-propylpentanoate
CAS Number 1069-66-5   Y ChemSpider 13428   Y UNII 5VOM6GYJ0D KEGG D00710   Y ChEBI CHEBI:9925   Y ChEMBL ChEMBL433   Y ECHA InfoCard 100.002.525 Chemical and physical data Formula C 8 H 15 Na O 2 Molar mass 166.20 g·mol −1 3D model ( JSmol ) Interactive image
InChI=1S/C8H16O2.Na/c1-3-5-7(6-4-2)8(9)10;/h7H,3-6H2,1-2H3,(H,9,10);/q;+1/p-1   Y Key:AEQFSUDEHCCHBT-UHFFFAOYSA-M   Y
Valproate exists in two main molecular variants: sodium valproate and valproic acid without sodium (often implied by simply valproate ). A mixture between these two is termed semisodium valproate. It is unclear whether there is any difference in efficacy between these variants, except from the fact that about 10% more of sodium valproate is needed than valproic acid without sodium to compensate for the sodium itself.
Brand names of valproic acid
Branded products include:
Absenor ( Orion Corporation Finland)
Convulex ( G.L. Pharma GmbH Austria)
Depakene ( Abbott Laboratories in US and Canada)
Depakine ( Sanofi Aventis France)
Depakine ( Sanofi Synthelabo Romania)
Depalept ( Sanofi Aventis Israel)
Deprakine ( Sanofi Aventis Finland)
Encorate ( Sun Pharmaceuticals India)
Epival ( Abbott Laboratories US and Canada)
Epilim ( Sanofi Synthelabo Australia and South Africa)
Stavzor ( Noven Pharmaceuticals Inc. )
Valcote ( Abbott Laboratories Argentina)
Valpakine ( Sanofi Aventis Brazil)
Orfiril ( Desitin Arzneimittel GmbH Norway)
Brand names of sodium valproate
Tablets – Diplexil-R by Bial.
United States
Intravenous injection – Depacon by Abbott Laboratories.
Syrup – Depakene by Abbott Laboratories. (Note Depakene capsules are valproic acid).
Depakote tablets are a mixture of sodium valproate and valproic acid.
Tablets – Eliaxim by Bial.
Epilim Crushable Tablets Sanofi
Epilim Sugar Free Liquid Sanofi
Epilim Syrup Sanofi
Epilim Tablets Sanofi
Sodium Valproate Sandoz Tablets Sanofi
Valpro Tablets Alphapharm
Valproate Winthrop Tablets Sanofi
Valprease tablets Sigma
New Zealand
Epilim by Sanofi-Aventis
All the above formulations are Pharmac -subsidised.
Depakote Tablets (as in USA)
Tablets – Orlept by Wockhardt and Epilim by Sanofi
Oral solution – Orlept Sugar Free by Wockhardt and Epilim by Sanofi
Syrup – Epilim by Sanofi-Aventis
Intravenous injection – Epilim Intravenous by Sanofi
Extended release tablets – Epilim Chrono by Sanofi is a combination of sodium valproate and valproic acid in a 2.3:1 ratio.
Enteric-coated tablets – Epilim EC200 by Sanofi is a 200-mg sodium valproate enteric-coated tablet.
UK only
Capsules – Episenta prolonged release by Beacon
Sachets – Episenta prolonged release by Beacon
Intravenous solution for injection – Episenta solution for injection by Beacon
Germany, Switzerland, Norway, Finland, Sweden
Tablets – Orfiril by Desitin Pharmaceuticals
Intravenous injection – Orfiril IV by Desitin Pharmaceuticals
South Africa
Syrup – Convulex by Byk Madaus
Tablets – Epilim by Sanofi-synthelabo
Tablets – Epilim by Sanofi-Aventis
Types are Syrup, Extended release mini tablets, Gastric resistant coated tablets, Gastric resistant soft capsules, Extended release capsules, Extended release tablets and Extended release coated tablets
Intravenous injection – Epival or Epiject by Abbott Laboratories.
Syrup – Depakene by Abbott Laboratories its generic formulations include Apo-Valproic and ratio-Valproic.
Tablets – Depakene by Kyowa Hakko Kirin
Extended release tablets – Depakene-R by Kyowa Hakko Kogyo and Selenica-R by Kowa
Syrup – Depakene by Kyowa Hakko Kogyo
In much of Europe, Dépakine and Depakine Chrono (tablets) are equivalent to Epilim and Epilim Chrono above.
Tablets (white round tablet) – Depakine ( Chinese : 帝拔癲 ; pinyin : di-ba-dian ) by Sanofi Winthrop Industrie (France)
Tablets –Epival 200 (enteric coated tablet) and Epival 500 (extended release tablet) by Iran Najo
Depalept and Depalept Chrono (extended release tablets) are equivalent to Epilim and Epilim Chrono above. Manufactured and distributed by Sanofi-Aventis.
India, Russia and CIS countries
Valprol CR by Intas Pharmaceutical (India)
Encorate Chrono by Sun Pharmaceutical (India)
Serven Chrono by Leeven APL Biotech (India)
Brand names of valproate semisodium
Brazil – Depakote by Abbott Laboratories and Torval CR by Torrent do Brasil
Canada – Epival by Abbott Laboratories
Mexico – Epival and Epival ER (extended release) by Abbott Laboratories
United Kingdom – Depakote (for psychiatric conditions) and Epilim (for epilepsy) by Sanofi-Aventis and generics
United States – Depakote and Depakote ER (extended release) by Abbott Laboratories and generics
India – Valance and Valance OD by Abbott Healthcare Pvt Ltd, Divalid ER by Linux laboratories Pvt Ltd, Valex ER by Sigmund Promedica, Dicorate by Sun Pharma
Germany – Ergenyl Chrono by Sanofi-Aventis and generics
Chile – Valcote and Valcote ER by Abbott Laboratories
France and other European countries — Depakote
Peru – Divalprax by AC Farma Laboratories
China – Diprate OD

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