Does BROMFENAC Cause Extra dose administered? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Extra dose administered have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 1.5% of all adverse event reports for BROMFENAC.
18
Reports of Extra dose administered with BROMFENAC
1.5%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Extra dose administered From BROMFENAC?
Of the 18 reports.
Is Extra dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BROMFENAC. However, 18 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 storage error (35)
What Other Drugs Cause Extra dose administered?
TIRZEPATIDE (6,774)
DULAGLUTIDE (3,047)
LORATADINE (1,556)
DUPILUMAB (1,422)
FEXOFENADINE (1,413)
NAPROXEN (908)
POLYETHYLENE GLYCOL 3350 (589)
ACETAMINOPHEN (552)
DALFAMPRIDINE (519)
FLUTICASONE\SALMETEROL (499)
Which BROMFENAC Alternatives Have Lower Extra dose administered Risk?
BROMFENAC vs BROMHEXINE
BROMFENAC vs BROMOCRIPTINE
BROMFENAC vs BROTIZOLAM
BROMFENAC vs BUCILLAMINE
BROMFENAC vs BUDESONIDE