VALPROIC ACID
Generic: VALPROIC ACID
ANI PharmaceuticalsManufacturer
ORALRoute
VALPROIC ACIDActive Substance
1992-08-25Original Approval
VALPROIC ACID is FDA application ANDA073178, sponsored by ANI PHARMS. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Top Reported Reactions
1
DRUG INEFFECTIVE
3,768 reports
2
DRUG INTERACTION
3,527 reports
3
OFF LABEL USE
2,159 reports
4
TOXICITY TO VARIOUS AGENTS
1,994 reports
5
SEIZURE
1,940 reports
6
COMPLETED SUICIDE
1,305 reports
7
SOMNOLENCE
1,276 reports
8
DEPRESSION
1,226 reports
9
CONDITION AGGRAVATED
1,053 reports
10
OVERDOSE
948 reports