Does OLOPATADINE Cause Product physical issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product physical issue have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 0.1% of all adverse event reports for OLOPATADINE.
7
Reports of Product physical issue with OLOPATADINE
0.1%
of all OLOPATADINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product physical issue From OLOPATADINE?
Of the 7 reports.
Is Product physical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 7 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 physical issue?
SUMATRIPTAN (2,349)
TIOTROPIUM (807)
ICOSAPENT ETHYL (666)
LISDEXAMFETAMINE DIMESYLATE (652)
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (387)
IBUPROFEN (337)
ESTRADIOL\LEVONORGESTREL (305)
ESTRADIOL (302)
RUXOLITINIB (302)
IXAZOMIB (298)
Which OLOPATADINE Alternatives Have Lower Product physical issue Risk?
OLOPATADINE vs OLUTASIDENIB
OLOPATADINE vs OMACETAXINE MEPESUCCINATE
OLOPATADINE vs OMADACYCLINE
OLOPATADINE vs OMALIZUMAB
OLOPATADINE vs OMAVELOXOLONE