Does LATANOPROSTENE BUNOD Cause Product use issue? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product use issue have been filed in association with LATANOPROSTENE BUNOD (Vyzulta). This represents 2.6% of all adverse event reports for LATANOPROSTENE BUNOD.
14
Reports of Product use issue with LATANOPROSTENE BUNOD
2.6%
of all LATANOPROSTENE BUNOD reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product use issue From LATANOPROSTENE BUNOD?
Of the 14 reports, 1 (7.1%) resulted in death, 1 (7.1%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROSTENE BUNOD. However, 14 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)
Product quality issue (29)
Vision blurred (28)
Death (27)
Headache (22)
Instillation site pain (21)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which LATANOPROSTENE BUNOD Alternatives Have Lower Product use issue Risk?
LATANOPROSTENE BUNOD vs LATANOPROST\NETARSUDIL
LATANOPROSTENE BUNOD vs LATANOPROST\TIMOLOL
LATANOPROSTENE BUNOD vs LATISSE
LATANOPROSTENE BUNOD vs LATUDA
LATANOPROSTENE BUNOD vs LAZERTINIB