Does LATANOPROST Cause Product physical consistency issue? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product physical consistency issue have been filed in association with LATANOPROST (IYUZEH). This represents 0.1% of all adverse event reports for LATANOPROST.
14
Reports of Product physical consistency issue with LATANOPROST
0.1%
of all LATANOPROST reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product physical consistency issue From LATANOPROST?
Of the 14 reports.
Is Product physical consistency issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROST. However, 14 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 physical consistency issue?
LEUPROLIDE (926)
CLASCOTERONE (317)
BUPRENORPHINE (242)
MINOXIDIL (171)
CHOLESTYRAMINE (141)
NAPROXEN (117)
TESTOSTERONE (113)
RUXOLITINIB (103)
DEVICE (85)
CLOBETASOL (76)
Which LATANOPROST Alternatives Have Lower Product physical consistency issue Risk?
LATANOPROST vs LATANOPROSTENE BUNOD
LATANOPROST vs LATANOPROST\NETARSUDIL
LATANOPROST vs LATANOPROST\TIMOLOL
LATANOPROST vs LATISSE
LATANOPROST vs LATUDA