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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BROMFENAC Cause Product physical consistency issue? 20 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Product physical consistency issue have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 1.7% of all adverse event reports for BROMFENAC.

20
Reports of Product physical consistency issue with BROMFENAC
1.7%
of all BROMFENAC reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product physical consistency issue From BROMFENAC?

Of the 20 reports.

Is Product physical consistency issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BROMFENAC. However, 20 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 physical consistency issue?

LEUPROLIDE (926) CLASCOTERONE (317) BUPRENORPHINE (242) MINOXIDIL (171) CHOLESTYRAMINE (141) NAPROXEN (117) TESTOSTERONE (113) RUXOLITINIB (103) DEVICE (85) CLOBETASOL (76)

Which BROMFENAC Alternatives Have Lower Product physical consistency issue Risk?

BROMFENAC vs BROMHEXINE BROMFENAC vs BROMOCRIPTINE BROMFENAC vs BROTIZOLAM BROMFENAC vs BUCILLAMINE BROMFENAC vs BUDESONIDE

Related Pages

BROMFENAC Full Profile All Product physical consistency issue Reports All Drugs Causing Product physical consistency issue BROMFENAC Demographics