Does OLOPATADINE Cause Product administration error? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product administration error have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 0.2% of all adverse event reports for OLOPATADINE.
13
Reports of Product administration error with OLOPATADINE
0.2%
of all OLOPATADINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From OLOPATADINE?
Of the 13 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 13 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which OLOPATADINE Alternatives Have Lower Product administration error Risk?
OLOPATADINE vs OLUTASIDENIB
OLOPATADINE vs OMACETAXINE MEPESUCCINATE
OLOPATADINE vs OMADACYCLINE
OLOPATADINE vs OMALIZUMAB
OLOPATADINE vs OMAVELOXOLONE