Does LATANOPROST Cause Product container issue? 158 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 158 reports of Product container issue have been filed in association with LATANOPROST (IYUZEH). This represents 1.0% of all adverse event reports for LATANOPROST.
158
Reports of Product container issue with LATANOPROST
1.0%
of all LATANOPROST reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product container issue From LATANOPROST?
Of the 158 reports, 4 (2.5%) required hospitalization.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROST. However, 158 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 container issue?
CYCLOSPORINE (910)
MINOXIDIL (556)
MOMETASONE FUROATE (450)
FORMOTEROL\MOMETASONE FUROATE (375)
LIFITEGRAST (244)
ALBUTEROL (192)
CARBOXYMETHYLCELLULOSE\GLYCERIN (123)
BRIMONIDINE (121)
ACETAMINOPHEN (118)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (102)
Which LATANOPROST Alternatives Have Lower Product container issue Risk?
LATANOPROST vs LATANOPROSTENE BUNOD
LATANOPROST vs LATANOPROST\NETARSUDIL
LATANOPROST vs LATANOPROST\TIMOLOL
LATANOPROST vs LATISSE
LATANOPROST vs LATUDA