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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 Treatment failure? 4,685 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 4,685 reports of Treatment failure have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 53.3% of all adverse event reports for OLOPATADINE.

4,685
Reports of Treatment failure with OLOPATADINE
53.3%
of all OLOPATADINE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Treatment failure From OLOPATADINE?

Of the 4,685 reports, 1 (0.0%) required hospitalization.

Is Treatment failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 4,685 reports have been filed with the FAERS database.

What Other Side Effects Does OLOPATADINE Cause?

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) Dry eye (132)

What Other Drugs Cause Treatment failure?

METHOTREXATE (14,672) ETANERCEPT (11,893) ADALIMUMAB (9,990) ABATACEPT (9,301) RITUXIMAB (9,217) TOCILIZUMAB (9,097) HYDROXYCHLOROQUINE (8,786) LEFLUNOMIDE (8,686) INFLIXIMAB (8,535) SULFASALAZINE (7,423)

Which OLOPATADINE Alternatives Have Lower Treatment failure Risk?

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

Related Pages

OLOPATADINE Full Profile All Treatment failure Reports All Drugs Causing Treatment failure OLOPATADINE Demographics