Does BROMFENAC Cause Product storage error? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Product storage error have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 3.0% of all adverse event reports for BROMFENAC.
35
Reports of Product storage error with BROMFENAC
3.0%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product storage error From BROMFENAC?
Of the 35 reports.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BROMFENAC. However, 35 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 use issue (39)
Product quality issue (34)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which BROMFENAC Alternatives Have Lower Product storage error Risk?
BROMFENAC vs BROMHEXINE
BROMFENAC vs BROMOCRIPTINE
BROMFENAC vs BROTIZOLAM
BROMFENAC vs BUCILLAMINE
BROMFENAC vs BUDESONIDE