Does BROMFENAC Cause Product use issue? 39 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Product use issue have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 3.3% of all adverse event reports for BROMFENAC.
39
Reports of Product use issue with BROMFENAC
3.3%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product use issue From BROMFENAC?
Of the 39 reports.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BROMFENAC. However, 39 reports have been filed with the FAERS database.
What Other Side Effects Does BROMFENAC Cause?
Treatment failure (152)
Eye irritation (118)
Off label use (115)
Eye pain (94)
Vision blurred (79)
Product packaging quantity issue (72)
Drug ineffective (63)
Product dose omission issue (55)
Product storage error (35)
Product quality issue (34)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which BROMFENAC Alternatives Have Lower Product use issue Risk?
BROMFENAC vs BROMHEXINE
BROMFENAC vs BROMOCRIPTINE
BROMFENAC vs BROTIZOLAM
BROMFENAC vs BUCILLAMINE
BROMFENAC vs BUDESONIDE