Does BROMFENAC Cause Product administration error? 8 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product administration error have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 0.7% of all adverse event reports for BROMFENAC.
8
Reports of Product administration error with BROMFENAC
0.7%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From BROMFENAC?
Of the 8 reports.
Is Product administration error 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which BROMFENAC Alternatives Have Lower Product administration error Risk?
BROMFENAC vs BROMHEXINE
BROMFENAC vs BROMOCRIPTINE
BROMFENAC vs BROTIZOLAM
BROMFENAC vs BUCILLAMINE
BROMFENAC vs BUDESONIDE