Does LATANOPROST Cause Product formulation issue? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Product formulation issue have been filed in association with LATANOPROST (IYUZEH). This represents 0.2% of all adverse event reports for LATANOPROST.
24
Reports of Product formulation issue with LATANOPROST
0.2%
of all LATANOPROST reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product formulation issue From LATANOPROST?
Of the 24 reports, 5 (20.8%) required hospitalization.
Is Product formulation issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROST. However, 24 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 formulation issue?
MINOXIDIL (1,369)
LEVOTHYROXINE (740)
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (174)
OMEPRAZOLE (99)
METHYLPHENIDATE (78)
OXYCODONE (73)
ACETAMINOPHEN\HYDROCODONE (62)
ACETAMINOPHEN\OXYCODONE (61)
ACETAMINOPHEN (59)
BUPROPION (59)
Which LATANOPROST Alternatives Have Lower Product formulation issue Risk?
LATANOPROST vs LATANOPROSTENE BUNOD
LATANOPROST vs LATANOPROST\NETARSUDIL
LATANOPROST vs LATANOPROST\TIMOLOL
LATANOPROST vs LATISSE
LATANOPROST vs LATUDA