RABEPRAZOLE SODIUM
Generic: RABEPRAZOLE SODIUM
Aurobindo Pharma LimitedManufacturer
ORALRoute
RABEPRAZOLE SODIUMActive Substance
2017-02-17Original Approval
RABEPRAZOLE SODIUM is FDA application ANDA205761, sponsored by QUAGEN. 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
DRUG INEFFECTIVE
1,925 reports
2
OFF LABEL USE
1,867 reports
3
NAUSEA
1,584 reports
4
DIARRHOEA
1,367 reports
5
HEADACHE
1,356 reports
6
PAIN
1,340 reports
7
DYSPNOEA
1,323 reports
8
ARTHRALGIA
1,304 reports
9
FATIGUE
1,241 reports
10
MALAISE
1,192 reports