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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 NEPAFENAC Cause Product administration error? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Product administration error have been filed in association with NEPAFENAC (ILEVRO). This represents 1.3% of all adverse event reports for NEPAFENAC.

23
Reports of Product administration error with NEPAFENAC
1.3%
of all NEPAFENAC reports
0
Deaths
8
Hospitalizations

How Dangerous Is Product administration error From NEPAFENAC?

Of the 23 reports, 8 (34.8%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NEPAFENAC. However, 23 reports have been filed with the FAERS database.

What Other Side Effects Does NEPAFENAC Cause?

Eye pain (393) Drug ineffective (270) Treatment failure (208) Vision blurred (133) Eye irritation (67) Visual impairment (66) Product quality issue (57) Liquid product physical issue (55) Off label use (43) Cystoid macular oedema (42)

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 NEPAFENAC Alternatives Have Lower Product administration error Risk?

NEPAFENAC vs NERATINIB NEPAFENAC vs NETARSUDIL NEPAFENAC vs NETUPITANT\PALONOSETRON NEPAFENAC vs NEULASTA NEPAFENAC vs NEUPOGEN

Related Pages

NEPAFENAC Full Profile All Product administration error Reports All Drugs Causing Product administration error NEPAFENAC Demographics