IBUPROFEN
Generic: IBUPROFEN, IBUPROFEN CAPSULE, LIQUID FILLED, IBUPROFEN CAPSULE
DOLGENCORP INCManufacturer
ORALRoute
IBUPROFENActive Substance
2009-03-24Original Approval
IBUPROFEN is FDA application ANDA078682, sponsored by BIONPHARMA. 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
15,701 reports
2
PAIN
15,069 reports
3
FATIGUE
14,487 reports
4
NAUSEA
13,515 reports
5
HEADACHE
12,096 reports
6
ARTHRALGIA
10,926 reports
7
DYSPNOEA
10,544 reports
8
VOMITING
9,991 reports
9
DIARRHOEA
9,708 reports
10
RASH
9,036 reports