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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 Extra dose administered? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Extra dose administered 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 Extra dose administered with OLOPATADINE
0.1%
of all OLOPATADINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Extra dose administered From OLOPATADINE?

Of the 8 reports.

Is Extra dose administered 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 Extra dose administered?

TIRZEPATIDE (6,774) DULAGLUTIDE (3,047) LORATADINE (1,556) DUPILUMAB (1,422) FEXOFENADINE (1,413) NAPROXEN (908) POLYETHYLENE GLYCOL 3350 (589) ACETAMINOPHEN (552) DALFAMPRIDINE (519) FLUTICASONE\SALMETEROL (499)

Which OLOPATADINE Alternatives Have Lower Extra dose administered Risk?

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

Related Pages

OLOPATADINE Full Profile All Extra dose administered Reports All Drugs Causing Extra dose administered OLOPATADINE Demographics