FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Generic: FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Aurobindo Pharma LimitedManufacturer
ORALRoute
FOSINOPRIL SODIUMActive Substance
2009-07-09Original Approval
FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE is FDA application ANDA079245, sponsored by AUROBINDO PHARMA. 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
FATIGUE
244 reports
2
DIARRHOEA
239 reports
3
DYSPNOEA
213 reports
4
NAUSEA
209 reports
5
DRUG INEFFECTIVE
186 reports
6
DIZZINESS
182 reports
7
ACUTE KIDNEY INJURY
179 reports
8
ASTHENIA
170 reports
9
RENAL FAILURE
164 reports
10
HYPOTENSION
145 reports