NAPROXEN SODIUM 220MG
Generic: NAPROXEN SODIUM 220MG, NAPROXEN SODIUM, NAPROXEN, NAPROXEN SODIUM, COATED TABLETS, NAPROXEN SODIUM TABLET, COATED, NAPROXEN SODIUM 220 MG
Allegiant HealthManufacturer
ORALRoute
NAPROXEN SODIUMActive Substance
2011-03-16Original Approval
NAPROXEN SODIUM 220MG is FDA application ANDA090545, sponsored by MARKSANS PHARMA. 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
2,935 reports
2
FATIGUE
2,689 reports
3
OFF LABEL USE
2,568 reports
4
PAIN
2,538 reports
5
RASH
2,331 reports
6
ARTHRALGIA
2,262 reports
7
DIARRHOEA
2,261 reports
8
VOMITING
2,205 reports
9
CONDITION AGGRAVATED
2,154 reports
10
JOINT SWELLING
2,134 reports