Does LATANOPROSTENE BUNOD Cause Product quality issue? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Product quality issue have been filed in association with LATANOPROSTENE BUNOD (Vyzulta). This represents 5.3% of all adverse event reports for LATANOPROSTENE BUNOD.
29
Reports of Product quality issue with LATANOPROSTENE BUNOD
5.3%
of all LATANOPROSTENE BUNOD reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product quality issue From LATANOPROSTENE BUNOD?
Of the 29 reports.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROSTENE BUNOD. However, 29 reports have been filed with the FAERS database.
What Other Side Effects Does LATANOPROSTENE BUNOD Cause?
Eye irritation (64)
Eye pain (56)
Ocular hyperaemia (56)
Intraocular pressure increased (43)
Drug ineffective (31)
Vision blurred (28)
Death (27)
Headache (22)
Instillation site pain (21)
Eye pruritus (20)
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 LATANOPROSTENE BUNOD Alternatives Have Lower Product quality issue Risk?
LATANOPROSTENE BUNOD vs LATANOPROST\NETARSUDIL
LATANOPROSTENE BUNOD vs LATANOPROST\TIMOLOL
LATANOPROSTENE BUNOD vs LATISSE
LATANOPROSTENE BUNOD vs LATUDA
LATANOPROSTENE BUNOD vs LAZERTINIB