Valproate

Valproate
INN: valproic acid
Names
Trade namesDepakote, Epilim, Convulex, others
Other namesValproic acid; Sodium valproate (sodium); Valproate semisodium (semisodium); 2-Propylvaleric acid
IUPAC name
  • 2-propylpentanoic acid
Clinical data
Pregnancy
category
  • AU: D
  • US: X (Contraindicated)- only for epilepsy or bipolar if other options are not possible[1]
    Routes of
    use    		By mouth, intravenous
    Defined daily dose1.5 g (by mouth) or
    1.5 g (parenteral) or
    1.5 g (rectal)[2]
    External links
    AHFS/Drugs.comMonograph
    MedlinePlusa682412
    Legal
    License data
    Legal status
    Pharmacokinetics
    BioavailabilityRapid absorption
    Protein binding80–90%[3]
    MetabolismLiver—glucuronide conjugation 30–50%, mitochondrial β-oxidation over 40%
    Elimination half-life9–16 hours[3]
    ExcretionUrine (30–50%)[3]
    Chemical and physical data
    FormulaC8H16O2
    Molar mass144.211 g·mol−1
    3D model (JSmol)
    SMILES
    • O=C(O)C(CCC)CCC
    InChI
    • InChI=1S/C8H16O2/c1-3-5-7(6-4-2)8(9)10/h7H,3-6H2,1-2H3,(H,9,10) checkY
    • Key:NIJJYAXOARWZEE-UHFFFAOYSA-N checkY

    Valproate (VPA) and its valproic acid, sodium valproate, and valproate semisodium forms are medications primarily used to treat epilepsy and bipolar disorder and prevent migraine headaches.[1] They are useful for the prevention of seizures in those with absence seizures, partial seizures, and generalized seizures.[1] They can be given intravenously or by mouth, and the tablet forms exist in both long- and short-acting formulations.[1]

    Common side effects of valproate include nausea, vomiting, sleepiness, and dry mouth.[1] Serious side effects can include liver failure, and regular monitoring of liver function tests is therefore recommended.[1] Other serious risks include pancreatitis and an increased suicide risk.[1] Valproate is known to cause serious abnormalities in babies if taken during pregnancy,[1][4] and as such it is not typically recommended for women of childbearing age who have migraines.[1]

    Valproate's precise mechanism of action is unclear.[1][5] Proposed mechanisms include affecting GABA levels, blocking voltage-gated sodium channels, and inhibiting histone deacetylases.[6][7] Valproic acid is a branched short-chain fatty acid (SCFA) made from valeric acid.[6]

    Valproate was first made in 1881 and came into medical use in 1962.[8] It is on the World Health Organization's List of Essential Medicines.[9] It is available as a generic medication.[1] The wholesale cost in the developing world is about US$0.40 per day as of 2015.[10] In the United States, the wholesale cost is roughly US$1.30 per day as of 2019.[11] It is marketed under the brand names Depakote, among others.[1] In 2017, it was the 126th most commonly prescribed medication in the United States, with more than five million prescriptions.[12][13]

    Terminology

    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.[14]

    Medical uses

    It is used primarily to treat epilepsy and bipolar disorder. It is also used to prevent migraine headaches.[15]

    Epilepsy

    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.[15][16] It has also been successfully given intravenously to treat status epilepticus.[17][18]

    Mental illness

    Bipolar disorder

    Valproate products are also used to treat manic or mixed episodes of bipolar disorder.[19][20]

    Schizophrenia

    A 2016 systematic review compared the efficacy of valproate as an add-on for people with schizophrenia:[21]

    There is limited evidence that adding valproate to antipsychotics may be effective for overall response and also for specific symptoms, especially in terms of excitement and aggression. Valproate was associated with a number of adverse events among which sedation and dizziness appeared more frequently than in the control groups.[21]

    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.[22][23][24]

    Migraines

    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.[25]

    Other

    The medication has been tested in the treatment of AIDS and cancer, owing to its histone-deacetylase-inhibiting effects.[26]

    Dosage

    The defined daily dose is 1.5 g (by mouth) or 1.5 g (parenteral) or 1.5 g (rectal)[2]

    For adults for seizures it is generally started at 300 mg twice per day.[27] This does is than increased by 200 mg every three days to 500 to 1000 mg twice per day.[27] The lower end of the dosing scale is generally used for bipolar.[27]

    For seizures, in children less than 20 kg, the dose is 10 mg/kg twice per day while the dose for children over 20 kg is 200 mg twice per day initially than increased to 10 to 15 mg per kg twice per day.[27]

    Side effects

    Valproate exacerbates methylmalonic aciduria. Note the periventricular white matter hyper intensities.
    See also: List of adverse effects of valproic acid and List of adverse effects of valproate semisodium

    Most common side effects include:[25]

    Serious adverse effects include:[25]

    Valproic acid has a black box warning for hepatotoxicity, pancreatitis, and fetal abnormalities.[25]

    There is evidence that valproic acid may cause premature growth plate ossification in children and adolescents, resulting in decreased height.[28][29][30][31] Valproic acid can also cause mydriasis, a dilation of the pupils.[32] There is evidence that shows valproic acid may increase the chance of polycystic ovary syndrome (PCOS) in women with epilepsy or bipolar disorder. Studies have shown this risk of PCOS is higher in women with epilepsy compared to those with bipolar disorder.[33] Weight gain is also possible.[34]

    Pregnancy

    Valproate causes birth defects;[35] exposure during pregnancy is associated with about three times as many major abnormalities as usual, mainly spina bifida with the risks being related to the strength of medication used and use of more than one drug.[36][37] More rarely, with several other defects, including a "valproate syndrome".[38] Characteristics of this valproate syndrome include facial features that tend to evolve with age, including a triangle-shaped forehead, tall forehead with bifrontal narrowing, epicanthic folds, medial deficiency of eyebrows, flat nasal bridge, broad nasal root, anteverted nares, shallow philtrum, long upper lip and thin vermillion borders, thick lower lip and small downturned mouth.[39] While developmental delay is usually associated with altered physical characteristics (dysmorphic features), this is not always the case.[40]

    Children of mothers taking valproate during pregnancy are at risk for lower IQs.[41][42][43] Maternal valproate use during pregnancy has been associated with a significantly higher probability of autism in the offspring.[44] A 2005 study found rates of autism among children exposed to sodium valproate before birth in the cohort studied were 8.9%.[45] The normal incidence for autism in the general population is estimated at less than one percent.[46] A 2009 study found that the 3-year-old children of pregnant women taking valproate had an IQ nine points lower than that of a well-matched control group. However, further research in older children and adults is needed.[47][48][49]

    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.[50][51]

    Women who intend to become pregnant should switch to a different medication if possible, or decrease their dose of valproate.[52] Women who become pregnant while taking valproate should be warned that it causes birth defects and cognitive impairment in the newborn, especially at high doses (although valproate is sometimes the only drug that can control seizures, and seizures in pregnancy could have even worse consequences). Studies have shown that taking folic acid can reduce the risk of congenital neural tube defects.[25] The use of valproate for migraine or bipolar disorder during pregnancy is contraindicated in the EU, and the medicines are not recommended for epilepsy during pregnancy unless there is no other effective treatment available.[53]

    Elderly

    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.[25]

    Contraindications

    Contraindications include:

    Interactions

    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.[54] It may also potentiate the CNS depressant effects of alcohol.[54] It should not be given in conjunction with other antiepileptics due to the potential for reduced clearance of other antiepileptics (including carbamazepine, lamotrigine, phenytoin and phenobarbitone) and itself.[54] It may also interact with:[25][54][56]

    • 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
    Form Lower limit Upper limit Unit
    Total (including
    protein bound)    		 50[57]125[57]µg/mL or mg/l
    350[58]700[58]μmol/L
    Free 6[57]22[57]µg/mL or mg/l
    35[58]70[58]μmol/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.[59] 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 (pKa of 4.9).[60]

    In severe intoxication, hemoperfusion or hemofiltration can be an effective means of hastening elimination of the drug from the body.[61][62] Supportive therapy should be given to all patients experiencing an overdose and urine output should be monitored.[25] Supplemental L-carnitine is indicated in patients having an acute overdose[63][64] and also prophylactically[63] in high risk patients. Acetyl-L-carnitine lowers hyperammonemia less markedly[65] than L-carnitine.

    Pharmacology

    Pharmacodynamics

    Although the mechanism of action of valproate is not fully understood,[54] traditionally, its anticonvulsant effect has been attributed to the blockade of voltage-gated sodium channels and increased brain levels of gamma-aminobutyric acid (GABA).[54] The GABAergic effect is also believed to contribute towards the anti-manic properties of valproate.[54] In animals, sodium valproate raises cerebral and cerebellar levels of the inhibitory synaptic neurotransmitter, GABA, possibly by inhibiting GABA degradative enzymes, such as GABA transaminase, succinate-semialdehyde dehydrogenase and by inhibiting the re-uptake of GABA by neuronal cells.[54]

    Prevention of neurotransmitter-induced hyperexcitability of nerve cells, via Kv7.2 channel and AKAP5, may also contribute to its mechanism.[66] Also, it has been shown to protect against a seizure-induced reduction in phosphatidylinositol (3,4,5)-trisphosphate (PIP3) as a potential therapeutic mechanism.[67]

    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.[68][69]

    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.[70] In addition, the drug has been identified as a potent aromatase inhibitor, and suppresses estrogen concentrations.[71] These actions are likely to be involved in the reproductive endocrine disturbances seen with valproic acid treatment.[70][71]

    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.[72][73] High rates of polycystic ovary syndrome and menstrual disorders have also been observed in women treated with valproic acid.[73]

    Metabolism

    The vast majority of valproate metabolism occurs in the liver.[74] In adult patients taking valproate alone, 30–50% of an administered dose is excreted in urine as a glucuronide conjugate.[74] The other major pathway in the metabolism of valproate is mitochondrial beta-oxidation, which typically accounts for over 40% of an administered dose.[74] Typically, less than 20% of an administered dose is eliminated by other oxidative mechanisms.[74] Less than 3% of an administered dose of valproate is excreted unchanged (i.e., as valproate) in urine.[74]

    Valproate is known to be metabolized by the Cytochrome P450 enzymes: CYP2A6, CYP2B6, CYP2C9, and CYP3A5.[74] It is also known to be metabolized by the UDP-glucuronosyltransferase enzymes: UGT1A3, UGT1A4, UGT1A6, UGT1A8, UGT1A9, UGT1A10, UGT2B7, and UGT2B15.[74] Some of the known metabolites of valproate by these enzymes and uncharacterized enzymes include: 2-ene-valproic acid, 3Z-ene-valproic acid, 3E-ene-valproic acid, 4-ene-valproic acid, valproic acid β-O-glucuronide, 3-oxovalproic acid, 3-hydroxyvalproic acid, 4-hydroxyvalproic acid, 5-hydroxyvalproic acid, and valproyl-CoA, among others.[74]

    Chemistry

    Valproic acid is a branched short-chain fatty acid and a derivative of valeric acid.[6]

    History

    Valproic acid was first synthesized in 1882 by Beverly S. Burton as an analogue of valeric acid, found naturally in valerian.[75] Valproic acid is a carboxylic acid, a clear liquid at room temperature. For many decades, its only use was in laboratories as a "metabolically inert" solvent for organic compounds. In 1962, the French researcher Pierre Eymard serendipitously discovered the anticonvulsant properties of valproic acid while using it as a vehicle for a number of other compounds that were being screened for antiseizure activity. He found it prevented pentylenetetrazol-induced convulsions in laboratory rats.[76] It was approved as an antiepileptic drug in 1967 in France and has become the most widely prescribed antiepileptic drug worldwide.[77] Valproic acid has also been used for migraine prophylaxis and bipolar disorder.[78]

    Society and culture

    Cost

    It is available as a generic medication.[1] The wholesale cost in the developing world is about US$0.40 per defined daily dose as of 2015.[10] In the United States, the National Average Drug Acquisition Cost is roughly US$1.30 per day for the short acting formulation as of 2019.[11] The price to a consumer in the United States for this amount is about $US2.30 per day as of 2019.[79] The long acting formulations are more expensive.[11] In the European Union, end-user costs are less than 0.60 EUR for an average daily dose in Germany.[80]

    • DivalproexSodium costs (US)
      DivalproexSodium costs (US)
    • DivalproexSodium prescriptions (US)
      DivalproexSodium prescriptions (US)

    Approval status

    Indications United States
    FDA-labelled indication?[3]    		 Australia
    TGA-labelled indication?[15]    		 United Kingdom
    MHRA-labelled indication?[81]    		 Literature support
    EpilepsyYesYesYesLimited (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).[82][83][84][85]
    Bipolar maniaYesYesYesLimited.[86]
    Bipolar depressionNoNoNoModerate.[87]
    Bipolar maintenanceNoNoNoLimited.[88]
    Migraine prophylaxisYesYes (accepted)NoLimited.
    Acute migraine managementNoNoNoOnly negative results.[89]
    SchizophreniaNoNoNoWeak evidence.[90]
    Agitation in dementiaNoNoNoWeak evidence. Not recommended for agitation in people with dementia.[91] Increased rate of adverse effects, including a risk of serious adverse effects.[91]
    Fragile X syndromeYes (orphan)NoNoLimited.[69]
    Familial adenomatous polyposisYes (orphan)NoNoLimited.
    Chronic pain & fibromyalgiaNoNoNoLimited.[92]
    Alcohol hallucinosisNoNoNoOne randomised double-blind placebo-controlled trial.[93]
    Intractable hiccupsNoNoNoLimited, five case reports support its efficacy, however.[94]
    Non-epileptic myoclonusNoNoNoLimited, three case reports support its efficacy, however.[95]
    Cluster headachesNoNoNoLimited, two case reports support its efficacy.[96]
    West syndromeNoNoNoA prospective clinical trial supported its efficacy in treating infantile spasms.[97]
    HIV infection eradicationNoNoNoDouble-blind placebo-controlled trials have been negative.[98][99][100]
    Myelodysplastic syndromeNoNoNoSeveral clinical trials have confirmed its efficacy as a monotherapy,[101] as an adjunct to tretinoin[101] and as an adjunct to hydralazine.[102]
    Acute myeloid leukaemiaNoNoNoTwo clinical trials have confirmed its efficacy in this indication as both a monotherapy and as an adjunct to tretinoin.[103][104][105]
    Cervical cancerNoNoNoOne clinical trial supports its use here.[106]
    Malignant melanomaNoNoNoOne phase II study has seemed to discount its efficacy.[107]
    Breast cancerNoNoNoA phase II study has supported its efficacy.[108]
    Impulse control disorderNoNoNoLimited.[109][110]

    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.[111][112]

    Formulations

    Sodium valproate
    Names
    Other namesvalproate sodium (USAN US)
    IUPAC name
    • sodium 2-propylpentanoate
    Legal
    License data
    Identifiers
    CAS Number
    • 1069-66-5 checkY
    PubChem CID
    DrugBank
    ChemSpider
    UNII
    KEGG
    ChEBI
    ChEMBL
    Chemical and physical data
    FormulaC8H15NaO2
    Molar mass166.196 g·mol−1
    3D model (JSmol)
    SMILES
    • CCCC(CCC)C(=O)[O-].[Na+]
    InChI
    • 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 checkY
    • Key:AEQFSUDEHCCHBT-UHFFFAOYSA-M checkY
    Valproate semisodium
    Names
    Trade namesDepakote, others
    Other namessemisodium valproate, divalproex sodium (USAN US)
    IUPAC name
    • sodium;2-propylpentanoate;2-propylpentanoic acid
    Legal
    License data
    Chemical and physical data
    FormulaC16H31NaO4
    Molar mass310.410 g·mol−1
    3D model (JSmol)
    SMILES
    • CCCC(CCC)C(=O)O.CCCC(CCC)C(=O)[O-].[Na+]
    InChI
    • InChI=1S/2C8H16O2.Na/c2*1-3-5-7(6-4-2)8(9)10;/h2*7H,3-6H2,1-2H3,(H,9,10);/q;;+1/p-1 checkY
    • Key:MSRILKIQRXUYCT-UHFFFAOYSA-M checkY

    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.[113]

    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)[114]
    • 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

    Portugal
    • 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.
    Australia
    • Epilim Crushable Tablets Sanofi[115]
    • Epilim Sugar Free Liquid Sanofi[115]
    • Epilim Syrup Sanofi[115]
    • Epilim Tablets Sanofi[115]
    • 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.[116]

    UK
    • 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[117]
    • Tablets – Epilim by Sanofi-synthelabo
    Malaysia
    • Tablets – Epilim by Sanofi-Aventis
    Romania
    • Companies are SANOFI-AVENTIS FRANCE, GEROT PHARMAZEUTIKA GMBH and DESITIN ARZNEIMITTEL GMBH
    • 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
    Canada
    • Intravenous injection – Epival or Epiject by Abbott Laboratories.
    • Syrup – Depakene by Abbott Laboratories its generic formulations include Apo-Valproic and ratio-Valproic.
    Japan
    • 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
    Europe

    In much of Europe, Dépakine and Depakine Chrono (tablets) are equivalent to Epilim and Epilim Chrono above.

    Taiwan
    • Tablets (white round tablet) – Depakine (Chinese: 帝拔癲; pinyin: di-ba-dian) by Sanofi Winthrop Industrie (France)
    Iran
    • Tablets – Epival 200 (enteric coated tablet) and Epival 500 (extended release tablet) by Iran Najo
    • Slow release tablets – Depakine Chrono by Sanofi Winthrop Industrie (France)
    Israel

    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
    • Valparin Chrono by Torrent Pharmaceuticals India
    • 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[25]
    • 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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    3. 1 2 3 4 "Depakene, Stavzor (valproic acid) dosing, indications, interactions, adverse effects, and more". Medscape Reference. WebMD. Archived from the original on 21 February 2014. Retrieved 13 February 2014.
    4. ↑ "Valproate banned without the pregnancy prevention programme". GOV.UK. Archived from the original on 24 April 2018. Retrieved 26 April 2018.
    5. ↑ Owens MJ, Nemeroff CB (2003). "Pharmacology of valproate". Psychopharmacol Bull. 37 Suppl 2: 17–24. PMID 14624230.
    6. 1 2 3 Ghodke-Puranik Y, Thorn CF, Lamba JK, Leeder JS, Song W, Birnbaum AK, Altman RB, Klein TE (April 2013). "Valproic acid pathway: pharmacokinetics and pharmacodynamics". Pharmacogenet. Genomics. 23 (4): 236–241. doi:10.1097/FPC.0b013e32835ea0b2. PMC 3696515. PMID 23407051.
    7. ↑ "Valproic acid". DrugBank. University of Alberta. 29 July 2017. Archived from the original on 31 July 2017. Retrieved 30 July 2017.
    8. ↑ Scott, D.F. (1993). The history of epileptic therapy : an account of how medication was developed (1. publ. ed.). Carnforth u.a.: Parthenon Publ. Group. p. 131. ISBN 9781850703914. Archived from the original on 2019-07-01. Retrieved 2017-09-17.
    9. ↑ World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
    10. 1 2 International Medical Products Price Guide (PDF) (2015 ed.). Management Sciences for Health. 2016. p. A-140. Archived from the original on 27 August 2021. Retrieved 23 February 2020.
    11. 1 2 3 "NADAC as of 2019-11-27 | Data.Medicaid.gov". Centers for Medicare and Medicaid Services. Archived from the original on 2020-07-11. Retrieved 25 November 2019.
    12. ↑ "The Top 300 of 2020". ClinCalc. Archived from the original on 18 March 2020. Retrieved 11 April 2020.
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