Does BROMFENAC Cause Wrong technique in product usage process? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Wrong technique in product usage process have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 0.7% of all adverse event reports for BROMFENAC.
8
Reports of Wrong technique in product usage process with BROMFENAC
0.7%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From BROMFENAC?
Of the 8 reports.
Is Wrong technique in product usage process 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which BROMFENAC Alternatives Have Lower Wrong technique in product usage process Risk?
BROMFENAC vs BROMHEXINE
BROMFENAC vs BROMOCRIPTINE
BROMFENAC vs BROTIZOLAM
BROMFENAC vs BUCILLAMINE
BROMFENAC vs BUDESONIDE