Does NERATINIB Cause Intentional product use issue? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Intentional product use issue have been filed in association with NERATINIB. This represents 1.4% of all adverse event reports for NERATINIB.
29
Reports of Intentional product use issue with NERATINIB
1.4%
of all NERATINIB reports
8
Deaths
19
Hospitalizations
How Dangerous Is Intentional product use issue From NERATINIB?
Of the 29 reports, 8 (27.6%) resulted in death, 19 (65.5%) required hospitalization, and 1 (3.4%) 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 NERATINIB. However, 29 reports have been filed with the FAERS database.
What Other Side Effects Does NERATINIB Cause?
Diarrhoea (1,193)
Nausea (527)
Fatigue (446)
Off label use (383)
Vomiting (297)
Constipation (267)
Decreased appetite (245)
Death (181)
Disease progression (142)
Weight decreased (132)
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 NERATINIB Alternatives Have Lower Intentional product use issue Risk?
NERATINIB vs NETARSUDIL
NERATINIB vs NETUPITANT\PALONOSETRON
NERATINIB vs NEULASTA
NERATINIB vs NEUPOGEN
NERATINIB vs NEUPRO