DUTASTERIDE
Generic: DUTASTERIDE
Banyan Pharma LLCManufacturer
ORALRoute
DUTASTERIDEActive Substance
2015-11-20Original Approval
DUTASTERIDE is FDA application ANDA204705, sponsored by PHARMOBEDIENT. 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
DYSPNOEA
803 reports
2
FATIGUE
627 reports
3
DIARRHOEA
558 reports
4
OFF LABEL USE
525 reports
5
ASTHENIA
510 reports
6
DIZZINESS
500 reports
7
FALL
477 reports
8
MALAISE
437 reports
9
CONDITION AGGRAVATED
434 reports
10
ASTHMA
422 reports