Does OLOPATADINE Cause Off label use? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Off label use have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 0.7% of all adverse event reports for OLOPATADINE.
59
Reports of Off label use with OLOPATADINE
0.7%
of all OLOPATADINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Off label use From OLOPATADINE?
Of the 59 reports, 1 (1.7%) required hospitalization.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 59 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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which OLOPATADINE Alternatives Have Lower Off label use Risk?
OLOPATADINE vs OLUTASIDENIB
OLOPATADINE vs OMACETAXINE MEPESUCCINATE
OLOPATADINE vs OMADACYCLINE
OLOPATADINE vs OMALIZUMAB
OLOPATADINE vs OMAVELOXOLONE