Does LATANOPROST Cause Product storage error? 149 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 149 reports of Product storage error have been filed in association with LATANOPROST (IYUZEH). This represents 1.0% of all adverse event reports for LATANOPROST.
149
Reports of Product storage error with LATANOPROST
1.0%
of all LATANOPROST reports
1
Deaths
5
Hospitalizations
How Dangerous Is Product storage error From LATANOPROST?
Of the 149 reports, 1 (0.7%) resulted in death, 5 (3.4%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROST. However, 149 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which LATANOPROST Alternatives Have Lower Product storage error Risk?
LATANOPROST vs LATANOPROSTENE BUNOD
LATANOPROST vs LATANOPROST\NETARSUDIL
LATANOPROST vs LATANOPROST\TIMOLOL
LATANOPROST vs LATISSE
LATANOPROST vs LATUDA