Does VERTEPORFIN Cause Intentional product use issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Intentional product use issue have been filed in association with VERTEPORFIN (Visudyne). This represents 1.2% of all adverse event reports for VERTEPORFIN.
9
Reports of Intentional product use issue with VERTEPORFIN
1.2%
of all VERTEPORFIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional product use issue From VERTEPORFIN?
Of the 9 reports.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VERTEPORFIN. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does VERTEPORFIN Cause?
Visual acuity reduced (173)
Off label use (129)
Polypoidal choroidal vasculopathy (128)
Disease progression (115)
Age-related macular degeneration (90)
Retinal haemorrhage (70)
Product use in unapproved indication (57)
Choroidal neovascularisation (47)
Retinal detachment (42)
Subretinal fluid (42)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which VERTEPORFIN Alternatives Have Lower Intentional product use issue Risk?
VERTEPORFIN vs VESICARE
VERTEPORFIN vs VFEND
VERTEPORFIN vs VIAGRA
VERTEPORFIN vs VIBEGRON
VERTEPORFIN vs VICODIN