CAPTOPRIL
Generic: CAPTOPRIL
Hikma Pharmaceuticals USA Inc.Manufacturer
ORALRoute
CAPTOPRILActive Substance
1996-02-13Original Approval
CAPTOPRIL is FDA application ANDA074505, sponsored by HIKMA INTL 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
DYSPNOEA
614 reports
2
DRUG INEFFECTIVE
601 reports
3
HYPERTENSION
536 reports
4
NAUSEA
508 reports
5
DIARRHOEA
470 reports
6
PAIN
455 reports
7
DIZZINESS
449 reports
8
ASTHENIA
425 reports
9
HEADACHE
401 reports
10
VOMITING
398 reports