IBUPROFEN AND FAMOTIDINE
Generic: IBUPROFEN AND FAMOTIDINE
Viona Pharmaceuticals IncManufacturer
ORALRoute
IBUPROFENActive Substance
2025-02-20Original Approval
IBUPROFEN AND FAMOTIDINE is FDA application ANDA218684, sponsored by ZYDUS LIFESCIENCES. 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
Top Reported Reactions
1
ARTHRALGIA
3 reports
2
PAIN
3 reports
3
ALOPECIA
2 reports
4
DRUG INEFFECTIVE
2 reports
5
RASH
2 reports
6
WHEEZING
2 reports
7
ABDOMINAL DISCOMFORT
1 reports
8
ABDOMINAL DISTENSION
1 reports
9
ANXIETY
1 reports
10
AVIAN INFLUENZA
1 reports