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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 Hypersensitivity? 269 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 269 reports of Hypersensitivity have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 3.1% of all adverse event reports for OLOPATADINE.

269
Reports of Hypersensitivity with OLOPATADINE
3.1%
of all OLOPATADINE reports
46
Deaths
67
Hospitalizations

How Dangerous Is Hypersensitivity From OLOPATADINE?

Of the 269 reports, 46 (17.1%) resulted in death, 67 (24.9%) required hospitalization.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 269 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) Ocular hyperaemia (260) Eye pain (228) Eye discharge (225) Eye swelling (143) Dry eye (132)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which OLOPATADINE Alternatives Have Lower Hypersensitivity Risk?

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

Related Pages

OLOPATADINE Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity OLOPATADINE Demographics