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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 Off label use? 115 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 115 reports of Off label use have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 9.7% of all adverse event reports for BROMFENAC.

115
Reports of Off label use with BROMFENAC
9.7%
of all BROMFENAC reports
0
Deaths
1
Hospitalizations

How Dangerous Is Off label use From BROMFENAC?

Of the 115 reports, 1 (0.9%) required hospitalization.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BROMFENAC. However, 115 reports have been filed with the FAERS database.

What Other Side Effects Does BROMFENAC Cause?

Treatment failure (152) Eye irritation (118) 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) Product quality issue (34)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Which BROMFENAC Alternatives Have Lower Off label use Risk?

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

Related Pages

BROMFENAC Full Profile All Off label use Reports All Drugs Causing Off label use BROMFENAC Demographics