Does LATANOPROST Cause Product use issue? 237 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 237 reports of Product use issue have been filed in association with LATANOPROST (IYUZEH). This represents 1.5% of all adverse event reports for LATANOPROST.
237
Reports of Product use issue with LATANOPROST
1.5%
of all LATANOPROST reports
2
Deaths
12
Hospitalizations
How Dangerous Is Product use issue From LATANOPROST?
Of the 237 reports, 2 (0.8%) resulted in death, 12 (5.1%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROST. However, 237 reports have been filed with the FAERS database.
What Other Side Effects Does LATANOPROST Cause?
Treatment failure (5,781)
Drug ineffective (1,338)
Eye irritation (1,165)
Eye pain (668)
Hypersensitivity (668)
Ocular hyperaemia (587)
Intraocular pressure increased (579)
Vision blurred (564)
Cataract (546)
Visual impairment (382)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which LATANOPROST Alternatives Have Lower Product use issue Risk?
LATANOPROST vs LATANOPROSTENE BUNOD
LATANOPROST vs LATANOPROST\NETARSUDIL
LATANOPROST vs LATANOPROST\TIMOLOL
LATANOPROST vs LATISSE
LATANOPROST vs LATUDA