Does BROMFENAC Cause Poor quality product administered? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Poor quality product administered have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 2.1% of all adverse event reports for BROMFENAC.
25
Reports of Poor quality product administered with BROMFENAC
2.1%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Poor quality product administered From BROMFENAC?
Of the 25 reports.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BROMFENAC. However, 25 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 Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
SOMATROPIN (234)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
Which BROMFENAC Alternatives Have Lower Poor quality product administered Risk?
BROMFENAC vs BROMHEXINE
BROMFENAC vs BROMOCRIPTINE
BROMFENAC vs BROTIZOLAM
BROMFENAC vs BUCILLAMINE
BROMFENAC vs BUDESONIDE