TORSEMIDE
Generic: TORSEMIDE
Chartwell RXManufacturer
ORALRoute
TORSEMIDEActive Substance
2005-05-31Original Approval
TORSEMIDE is FDA application ANDA076894, sponsored by COREPHARMA. 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
3,494 reports
2
FATIGUE
2,186 reports
3
DIARRHOEA
2,061 reports
4
NAUSEA
2,031 reports
5
DIZZINESS
1,932 reports
6
ACUTE KIDNEY INJURY
1,789 reports
7
DEATH
1,719 reports
8
GENERAL PHYSICAL HEALTH DETERIORATION
1,649 reports
9
FALL
1,626 reports
10
OEDEMA PERIPHERAL
1,582 reports