BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Generic: BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
ANI PharmaceuticalsManufacturer
ORALRoute
BENAZEPRIL HYDROCHLORIDEActive Substance
2004-02-11Original Approval
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE is FDA application ANDA076342, sponsored by ANI 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
DIARRHOEA
13 reports
2
DIZZINESS
11 reports
3
NAUSEA
10 reports
4
DRUG INEFFECTIVE
9 reports
5
FATIGUE
9 reports
6
PAIN
9 reports
7
DYSPNOEA
8 reports
8
OFF LABEL USE
8 reports
9
ASTHENIA
7 reports
10
CEREBROVASCULAR ACCIDENT
7 reports