Does COBIMETINIB Cause Intentional product use issue? 101 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 101 reports of Intentional product use issue have been filed in association with COBIMETINIB (Cotellic). This represents 2.5% of all adverse event reports for COBIMETINIB.
101
Reports of Intentional product use issue with COBIMETINIB
2.5%
of all COBIMETINIB reports
21
Deaths
13
Hospitalizations
How Dangerous Is Intentional product use issue From COBIMETINIB?
Of the 101 reports, 21 (20.8%) resulted in death, 13 (12.9%) required hospitalization, and 1 (1.0%) 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 COBIMETINIB. However, 101 reports have been filed with the FAERS database.
What Other Side Effects Does COBIMETINIB Cause?
Diarrhoea (412)
Off label use (411)
Rash (369)
Pyrexia (332)
Death (231)
Nausea (206)
Fatigue (198)
No adverse event (178)
Vomiting (168)
Acute kidney injury (133)
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 COBIMETINIB Alternatives Have Lower Intentional product use issue Risk?
COBIMETINIB vs COCAETHYLENE
COBIMETINIB vs COCAINE
COBIMETINIB vs COCOA BUTTER\PHENYLEPHRINE
COBIMETINIB vs COD LIVER OIL
COBIMETINIB vs CODEINE