Does BROMFENAC Cause Product packaging quantity issue? 72 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 72 reports of Product packaging quantity issue have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 6.1% of all adverse event reports for BROMFENAC.
72
Reports of Product packaging quantity issue with BROMFENAC
6.1%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product packaging quantity issue From BROMFENAC?
Of the 72 reports.
Is Product packaging quantity issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BROMFENAC. However, 72 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)
Drug ineffective (63)
Product dose omission issue (55)
Product use issue (39)
Product storage error (35)
Product quality issue (34)
What Other Drugs Cause Product packaging quantity issue?
LEUPROLIDE (523)
ALBUTEROL (431)
BUDESONIDE\FORMOTEROL (301)
FENTANYL (286)
BUPRENORPHINE (225)
CYCLOSPORINE (206)
ESTRADIOL (201)
BIMATOPROST (177)
RIVAROXABAN (174)
EXENATIDE (154)
Which BROMFENAC Alternatives Have Lower Product packaging quantity issue Risk?
BROMFENAC vs BROMHEXINE
BROMFENAC vs BROMOCRIPTINE
BROMFENAC vs BROTIZOLAM
BROMFENAC vs BUCILLAMINE
BROMFENAC vs BUDESONIDE