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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 Mydriasis? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Mydriasis have been filed in association with BROMFENAC (BROMFENAC SODIUM). This represents 0.7% of all adverse event reports for BROMFENAC.

8
Reports of Mydriasis with BROMFENAC
0.7%
of all BROMFENAC reports
0
Deaths
1
Hospitalizations

How Dangerous Is Mydriasis From BROMFENAC?

Of the 8 reports, 1 (12.5%) required hospitalization.

Is Mydriasis 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 Mydriasis?

VENLAFAXINE (499) SERTRALINE (417) DIAZEPAM (400) QUETIAPINE (395) ACETAMINOPHEN (387) PREGABALIN (356) NAPHAZOLINE\PHENIRAMINE (353) TRAMADOL (338) ALPRAZOLAM (320) GLYCOPYRRONIUM (280)

Which BROMFENAC Alternatives Have Lower Mydriasis Risk?

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

Related Pages

BROMFENAC Full Profile All Mydriasis Reports All Drugs Causing Mydriasis BROMFENAC Demographics