Does OLOPATADINE Cause Product label issue? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product label issue have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 0.1% of all adverse event reports for OLOPATADINE.
6
Reports of Product label issue with OLOPATADINE
0.1%
of all OLOPATADINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product label issue From OLOPATADINE?
Of the 6 reports.
Is Product label issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 6 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 Product label issue?
RIVAROXABAN (379)
ACETAMINOPHEN (276)
GUSELKUMAB (177)
USTEKINUMAB (164)
DIMETHICONE\LOPERAMIDE (154)
CETIRIZINE (138)
IBUPROFEN (99)
GOLIMUMAB (76)
POLYETHYLENE GLYCOL 3350 (76)
FENTANYL (72)
Which OLOPATADINE Alternatives Have Lower Product label issue Risk?
OLOPATADINE vs OLUTASIDENIB
OLOPATADINE vs OMACETAXINE MEPESUCCINATE
OLOPATADINE vs OMADACYCLINE
OLOPATADINE vs OMALIZUMAB
OLOPATADINE vs OMAVELOXOLONE