MOEXIPRIL HYDROCHLORIDE
Generic: MOEXIPRIL HYDROCHLORIDE
Chartwell RXManufacturer
ORALRoute
MOEXIPRIL HYDROCHLORIDEActive Substance
2006-11-30Original Approval
MOEXIPRIL HYDROCHLORIDE is FDA application ANDA077536, sponsored by CHARTWELL RX. 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
ASTHENIA
8 reports
2
DYSPNOEA
6 reports
3
NAUSEA
5 reports
4
BLOOD PRESSURE DECREASED
4 reports
5
CEREBROVASCULAR ACCIDENT
4 reports
6
COUGH
4 reports
7
DEHYDRATION
4 reports
8
DIARRHOEA
4 reports
9
DRUG INEFFECTIVE
4 reports
10
FLUSHING
4 reports