DULOXETINE HYDROCHLORIDE
Generic: DULOXETINE HYDROCHLORIDE
Macleods Pharmaceuticals LimitedManufacturer
ORALRoute
DULOXETINE HYDROCHLORIDEActive Substance
2017-03-23Original Approval
DULOXETINE HYDROCHLORIDE is FDA application ANDA204815, sponsored by MACLEODS 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
5,434 reports
2
NAUSEA
5,136 reports
3
FATIGUE
5,059 reports
4
OFF LABEL USE
4,390 reports
5
PAIN
3,915 reports
6
HEADACHE
3,912 reports
7
DIARRHOEA
3,507 reports
8
DIZZINESS
3,218 reports
9
FALL
2,948 reports
10
VOMITING
2,624 reports