Does LATANOPROST Cause Product quality issue? 332 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 332 reports of Product quality issue have been filed in association with LATANOPROST (IYUZEH). This represents 2.2% of all adverse event reports for LATANOPROST.
332
Reports of Product quality issue with LATANOPROST
2.2%
of all LATANOPROST reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product quality issue From LATANOPROST?
Of the 332 reports, 7 (2.1%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROST. However, 332 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which LATANOPROST Alternatives Have Lower Product quality issue Risk?
LATANOPROST vs LATANOPROSTENE BUNOD
LATANOPROST vs LATANOPROST\NETARSUDIL
LATANOPROST vs LATANOPROST\TIMOLOL
LATANOPROST vs LATISSE
LATANOPROST vs LATUDA