Does BROMFENAC Cause Incorrect drug administration duration? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Incorrect drug administration duration have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 0.7% of all adverse event reports for BROMFENAC.
8
Reports of Incorrect drug administration duration with BROMFENAC
0.7%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect drug administration duration From BROMFENAC?
Of the 8 reports.
Is Incorrect drug administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BROMFENAC. However, 8 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 Incorrect drug administration duration?
ETONOGESTREL (1,796)
POLYETHYLENE GLYCOL 3350 (1,722)
NAPROXEN (1,272)
DOCOSANOL (803)
ETHINYL ESTRADIOL\ETONOGESTREL (740)
NICOTINE (561)
RANITIDINE (504)
GUAIFENESIN (490)
INSULIN LISPRO (367)
ACETAMINOPHEN (340)
Which BROMFENAC Alternatives Have Lower Incorrect drug administration duration Risk?
BROMFENAC vs BROMHEXINE
BROMFENAC vs BROMOCRIPTINE
BROMFENAC vs BROTIZOLAM
BROMFENAC vs BUCILLAMINE
BROMFENAC vs BUDESONIDE