Does OLOPATADINE Cause Device defective? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device defective have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 0.1% of all adverse event reports for OLOPATADINE.
5
Reports of Device defective with OLOPATADINE
0.1%
of all OLOPATADINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device defective From OLOPATADINE?
Of the 5 reports.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 5 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which OLOPATADINE Alternatives Have Lower Device defective Risk?
OLOPATADINE vs OLUTASIDENIB
OLOPATADINE vs OMACETAXINE MEPESUCCINATE
OLOPATADINE vs OMADACYCLINE
OLOPATADINE vs OMALIZUMAB
OLOPATADINE vs OMAVELOXOLONE