OXAPROZIN
Generic: OXAPROZIN
Dr. Reddy's Laboratories LimitedManufacturer
ORALRoute
OXAPROZINActive Substance
2001-01-31Original Approval
OXAPROZIN is FDA application ANDA075855, sponsored by DR REDDYS LABS 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
CHRONIC KIDNEY DISEASE
82 reports
2
DRUG INEFFECTIVE
68 reports
3
PAIN
68 reports
4
DRUG HYPERSENSITIVITY
61 reports
5
NAUSEA
60 reports
6
RENAL FAILURE
54 reports
7
ACUTE KIDNEY INJURY
51 reports
8
ARTHRALGIA
50 reports
9
DIZZINESS
48 reports
10
FATIGUE
42 reports