Does LATANOPROSTENE BUNOD Cause Off label use? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Off label use have been filed in association with LATANOPROSTENE BUNOD (Vyzulta). This represents 1.3% of all adverse event reports for LATANOPROSTENE BUNOD.
7
Reports of Off label use with LATANOPROSTENE BUNOD
1.3%
of all LATANOPROSTENE BUNOD reports
1
Deaths
3
Hospitalizations
How Dangerous Is Off label use From LATANOPROSTENE BUNOD?
Of the 7 reports, 1 (14.3%) resulted in death, 3 (42.9%) required hospitalization.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROSTENE BUNOD. However, 7 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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which LATANOPROSTENE BUNOD Alternatives Have Lower Off label use Risk?
LATANOPROSTENE BUNOD vs LATANOPROST\NETARSUDIL
LATANOPROSTENE BUNOD vs LATANOPROST\TIMOLOL
LATANOPROSTENE BUNOD vs LATISSE
LATANOPROSTENE BUNOD vs LATUDA
LATANOPROSTENE BUNOD vs LAZERTINIB