Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Divalproex sodium
Drug ID BADD_D00696
Description Valproic acid, or valproate, is an fatty acid derivative and anticonvulsant originally synthesized in 1881 by Beverly S. Burton.[A178051] It enjoyed use as a popular organic solvent in industry and pharmaceutical manufacturing for nearly a century. In 1963, a serendipitous discovery was made by George Carraz during his investigations into the anticonvulsant effects of khelline when he found that all of his samples, dissolved in valproic acid, exerted a similar degree of anticonvulsive activity. It first received approval on February 28, 1978 from the FDA under the trade name Depakene.[L6190] Since then, it has been investigated for neuroprotective, anti-manic, and anti-migraine effects. It is currently a compound of interest in the field of oncology for its anti-proliferative effects and is the subject of many clinical trials in a variety of cancer types.
Indications and Usage For treatment and management of seizure disorders, mania, and prophylactic treatment of migraine headache. In epileptics, valproic acid is used to control absence seizures, tonic-clonic seizures (grand mal), complex partial seizures, and the seizures associated with Lennox-Gastaut syndrome.
Marketing Status Prescription; Discontinued
ATC Code N03AG01
DrugBank ID DB00313
KEGG ID D00304
MeSH ID D014635
PubChem ID 23663956
TTD Drug ID D03LGY
NDC Product Code 55111-530; 70518-1749; 65862-959; 0904-6615; 55111-529; 68084-782; 63187-742; 65162-755; 71610-032; 68788-7183; 71335-1883; 50090-4409; 68084-776; 57237-047; 64679-724; 51079-766; 29300-138; 55154-5633; 0615-8326; 70518-2527; 50090-3616; 55111-534; 71610-031; 29300-380; 70518-0312; 50090-2795; 68084-313; 68001-472; 68001-473; 63629-4278; 51655-365; 70518-0282; 0615-8237; 55154-2336; 71335-0008; 70518-2036; 70518-2626; 67296-1677; 0615-8329; 66064-1001; 29300-381; 70518-2665; 23639-0001; 0074-6114; 57237-048; 68180-265; 55111-532; 0832-7124; 55700-938; 68071-4102; 68001-106; 0904-6861; 68382-134; 70518-3055; 70518-0463; 55154-4759; 65862-594; 62756-797; 0074-7325; 70518-1759; 65841-639; 68382-133; 68382-032; 50268-258; 70518-2357; 71610-157; 70518-1558; 0074-7402; 16714-485; 65841-637; 70518-3183; 0074-6214; 51079-767; 68382-033; 50090-3416; 55700-939; 70518-2513; 55111-533; 0832-7123; 71610-249; 70518-1897; 71610-289; 0074-6215; 48433-125; 71610-205; 48433-126; 71610-311; 68382-106; 65862-402; 68180-260; 70518-3364; 70518-2003; 0904-6363; 65862-975; 68788-7177; 55154-4679; 71610-201; 63187-743; 68001-474; 0904-6364; 65841-638; 70518-1138; 62756-798; 63629-4698; 65841-634; 17856-0262; 65862-595; 68788-8145; 55154-7640; 68108-0234; 16714-484; 68084-415; 27241-115; 68180-261; 50090-4187; 0378-0472; 0904-6860; 55111-531; 70518-1781; 65977-0114; 68382-031; 65841-635; 67296-1635; 0832-7122; 70518-1456; 49452-2542; 0615-8377; 55154-7145; 0074-7327; 50090-4861; 0074-7401; 60687-211; 17349-0011; 68001-105; 50090-5843; 64679-725; 55111-875; 58118-0040; 50090-5783; 70518-2510; 68925-0005; 68788-8085; 71610-030; 68180-267; 70518-1758; 65162-757; 70518-1556; 62756-796; 47621-006; 0615-8328; 0378-0473; 70600-016; 70518-0374; 43353-547; 17856-0109; 0074-3826; 70518-2674; 57237-106; 29300-140; 49169-1028; 65841-636; 0615-8327; 68180-266; 50090-4737; 61919-648; 29300-139; 50090-2007; 55154-3552; 0615-8376; 65862-403; 0615-8330; 0074-7126; 50090-5842; 68084-310; 0074-6212
Synonyms Valproic Acid | 2-Propylpentanoic Acid | 2 Propylpentanoic Acid | Divalproex | Depakene | Convulsofin | Depakote | Dipropyl Acetate | Divalproex Sodium | Semisodium Valproate | Vupral | Valproic Acid, Sodium Salt (2:1) | Propylisopropylacetic Acid | Ergenyl | Magnesium Valproate | Valproate | Valproate Sodium | Sodium Valproate | Calcium Valproate | Valproate Calcium | Depakine
Chemical Information
Molecular Formula C16H31NaO4
CAS Registry Number 76584-70-8
SMILES CCCC(CCC)C(=O)O.CCCC(CCC)C(=O)[O-].[Na+]
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Adverse drug reactionCytochrome P450 1A2P05177Not AvailableNot Available
HepatotoxicityCytochrome P450 2A6P11509T06455Not Available
HepatotoxicityCytochrome P450 2E1P05181Not AvailableNot Available
HepatotoxicityCytochrome P450 2C9P11712T19244Not Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal pain07.01.05.002--
Abnormal dreams19.02.03.001; 17.15.02.001--Not Available
Aggression19.05.01.001--Not Available
Agitation19.06.02.001; 17.02.05.012--
Agranulocytosis01.02.03.001--Not Available
Alanine aminotransferase increased13.03.01.003--
Alopecia23.02.02.001--
Amblyopia06.02.01.001--Not Available
Amenorrhoea21.01.02.001; 05.05.01.002--
Amnesia19.20.01.001; 17.03.02.001--
Anaemia01.03.02.001--
Anaemia macrocytic14.12.01.002; 01.03.02.002--Not Available
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Anxiety19.06.02.002--
Aplastic anaemia01.03.03.002--Not Available
Arrhythmia02.03.02.001--Not Available
Arthralgia15.01.02.001--
Aspartate aminotransferase increased13.03.01.006--
Asterixis17.01.06.001; 09.01.03.004--Not Available
Asthenia08.01.01.001--Not Available
Ataxia17.02.02.001; 08.01.02.004--
Back pain15.03.04.005--
Bleeding time prolonged13.01.02.002--Not Available
Blood bilirubin increased13.03.01.008--
Blood lactate dehydrogenase increased13.04.02.002--
Bone pain15.02.01.001--
Bradycardia02.03.02.002--Not Available
Breast enlargement21.05.04.001--Not Available
Bronchitis22.07.01.001; 11.01.09.001--
Carnitine decreased13.12.02.003--Not Available
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