IBUPROFEN MINIS
Generic: IBUPROFEN
Aurohealth LLCManufacturer
ORALRoute
IBUPROFENActive Substance
2023-09-14Original Approval
IBUPROFEN MINIS is FDA application ANDA215777, sponsored by AUROBINDO PHARMA LTD. 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
15,703 reports
2
PAIN
15,060 reports
3
FATIGUE
14,475 reports
4
NAUSEA
13,506 reports
5
HEADACHE
12,086 reports
6
ARTHRALGIA
10,919 reports
7
DYSPNOEA
10,527 reports
8
VOMITING
9,974 reports
9
DIARRHOEA
9,701 reports
10
RASH
9,031 reports