Does OLOPATADINE Cause Condition aggravated? 116 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 116 reports of Condition aggravated have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 1.3% of all adverse event reports for OLOPATADINE.
116
Reports of Condition aggravated with OLOPATADINE
1.3%
of all OLOPATADINE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Condition aggravated From OLOPATADINE?
Of the 116 reports, 4 (3.4%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 116 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which OLOPATADINE Alternatives Have Lower Condition aggravated Risk?
OLOPATADINE vs OLUTASIDENIB
OLOPATADINE vs OMACETAXINE MEPESUCCINATE
OLOPATADINE vs OMADACYCLINE
OLOPATADINE vs OMALIZUMAB
OLOPATADINE vs OMAVELOXOLONE