ACID REDUCER

Generic: FAMOTIDINE

Publix Super Markets IncManufacturer
ORALRoute
FAMOTIDINEActive Substance
2006-09-25Original Approval

ACID REDUCER is FDA application ANDA077351, sponsored by PERRIGO R AND D. 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.

Recalls

Class II2021-10-05
Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium), 24 Hour, 14-count capsules pe

CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the

Top Reported Reactions

1
NAUSEA
34,434 reports
2
DIARRHOEA
34,260 reports
3
FATIGUE
33,191 reports
4
DYSPNOEA
29,090 reports
5
DRUG INEFFECTIVE
27,362 reports
6
HEADACHE
26,015 reports
7
OFF LABEL USE
25,705 reports
8
VOMITING
23,963 reports
9
PAIN
23,285 reports
10
DIZZINESS
21,838 reports