IBUPROFEN
Generic: IBUPROFEN, IBUPROFEN 200MG
Harris TeeterManufacturer
ORALRoute
IBUPROFENActive Substance
2016-10-07Original Approval
IBUPROFEN is FDA application ANDA202312, sponsored by GRANULES. 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
15,706 reports
2
PAIN
15,062 reports
3
FATIGUE
14,482 reports
4
NAUSEA
13,513 reports
5
HEADACHE
12,097 reports
6
ARTHRALGIA
10,921 reports
7
DYSPNOEA
10,535 reports
8
VOMITING
9,981 reports
9
DIARRHOEA
9,708 reports
10
RASH
9,038 reports