ESCITALOPRAM OXALATE
Generic: ESCITALOPRAM
Amneal Pharmaceuticals LLCManufacturer
ORALRoute
ESCITALOPRAM OXALATEActive Substance
2012-03-14Original Approval
ESCITALOPRAM OXALATE is FDA application ANDA202227, sponsored by AMNEAL 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
4,822 reports
2
FATIGUE
4,607 reports
3
NAUSEA
4,375 reports
4
OFF LABEL USE
3,899 reports
5
HEADACHE
3,746 reports
6
DIARRHOEA
3,735 reports
7
DRUG INTERACTION
3,118 reports
8
DIZZINESS
3,098 reports
9
FALL
3,061 reports
10
ANXIETY
2,977 reports