Does VEMURAFENIB Cause Intentional product use issue? 251 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 251 reports of Intentional product use issue have been filed in association with VEMURAFENIB (ZELBORAF). This represents 2.9% of all adverse event reports for VEMURAFENIB.
251
Reports of Intentional product use issue with VEMURAFENIB
2.9%
of all VEMURAFENIB reports
42
Deaths
38
Hospitalizations
How Dangerous Is Intentional product use issue From VEMURAFENIB?
Of the 251 reports, 42 (16.7%) resulted in death, 38 (15.1%) required hospitalization, and 2 (0.8%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VEMURAFENIB. However, 251 reports have been filed with the FAERS database.
What Other Side Effects Does VEMURAFENIB Cause?
Rash (1,202)
Arthralgia (783)
Off label use (782)
Fatigue (773)
Diarrhoea (655)
Nausea (601)
Pyrexia (569)
Death (505)
Alopecia (445)
Decreased appetite (383)
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 VEMURAFENIB Alternatives Have Lower Intentional product use issue Risk?
VEMURAFENIB vs VENETOCLAX
VEMURAFENIB vs VENLAFAXINE
VEMURAFENIB vs VENTAVIS
VEMURAFENIB vs VENTOLIN
VEMURAFENIB vs VENTOLIN HFA