Does BROMFENAC Cause Product dose omission issue? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Product dose omission issue have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 4.6% of all adverse event reports for BROMFENAC.
55
Reports of Product dose omission issue with BROMFENAC
4.6%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission issue From BROMFENAC?
Of the 55 reports.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BROMFENAC. However, 55 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 use issue (39)
Product storage error (35)
Product quality issue (34)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which BROMFENAC Alternatives Have Lower Product dose omission issue Risk?
BROMFENAC vs BROMHEXINE
BROMFENAC vs BROMOCRIPTINE
BROMFENAC vs BROTIZOLAM
BROMFENAC vs BUCILLAMINE
BROMFENAC vs BUDESONIDE