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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 OLOPATADINE Cause Hepatic function abnormal? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Hepatic function abnormal have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 0.1% of all adverse event reports for OLOPATADINE.

8
Reports of Hepatic function abnormal with OLOPATADINE
0.1%
of all OLOPATADINE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Hepatic function abnormal From OLOPATADINE?

Of the 8 reports, 5 (62.5%) required hospitalization, and 1 (12.5%) were considered life-threatening.

Is Hepatic function abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does OLOPATADINE Cause?

Treatment failure (4,685) Drug ineffective (1,600) Eye irritation (554) Vision blurred (368) Eye pruritus (317) Hypersensitivity (269) Ocular hyperaemia (260) Eye pain (228) Eye discharge (225) Eye swelling (143)

What Other Drugs Cause Hepatic function abnormal?

NIVOLUMAB (1,131) PEMBROLIZUMAB (1,079) METHOTREXATE (1,054) CABOZANTINIB S-MALATE (912) CYCLOPHOSPHAMIDE (824) BEVACIZUMAB (769) PACLITAXEL (603) LENVATINIB (528) ATORVASTATIN (520) CYCLOSPORINE (508)

Which OLOPATADINE Alternatives Have Lower Hepatic function abnormal Risk?

OLOPATADINE vs OLUTASIDENIB OLOPATADINE vs OMACETAXINE MEPESUCCINATE OLOPATADINE vs OMADACYCLINE OLOPATADINE vs OMALIZUMAB OLOPATADINE vs OMAVELOXOLONE

Related Pages

OLOPATADINE Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal OLOPATADINE Demographics