Does OLOPATADINE Cause Ocular hyperaemia? 260 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 260 reports of Ocular hyperaemia have been filed in association with OLOPATADINE (PATADAY ONCE DAILY RELIEF). This represents 3.0% of all adverse event reports for OLOPATADINE.
260
Reports of Ocular hyperaemia with OLOPATADINE
3.0%
of all OLOPATADINE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Ocular hyperaemia From OLOPATADINE?
Of the 260 reports, 1 (0.4%) resulted in death, 2 (0.8%) required hospitalization.
Is Ocular hyperaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLOPATADINE. However, 260 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)
Eye pain (228)
Eye discharge (225)
Eye swelling (143)
Dry eye (132)
What Other Drugs Cause Ocular hyperaemia?
DUPILUMAB (6,938)
CYCLOSPORINE (1,508)
BIMATOPROST (1,447)
CENEGERMIN-BKBJ (1,226)
BRIMONIDINE (917)
ADALIMUMAB (714)
LATANOPROST (587)
DORZOLAMIDE\TIMOLOL (581)
LIFITEGRAST (570)
TRAVOPROST (478)
Which OLOPATADINE Alternatives Have Lower Ocular hyperaemia Risk?
OLOPATADINE vs OLUTASIDENIB
OLOPATADINE vs OMACETAXINE MEPESUCCINATE
OLOPATADINE vs OMADACYCLINE
OLOPATADINE vs OMALIZUMAB
OLOPATADINE vs OMAVELOXOLONE