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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does NERATINIB Cause Product use issue? 60 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 60 reports of Product use issue have been filed in association with NERATINIB. This represents 2.9% of all adverse event reports for NERATINIB.

60
Reports of Product use issue with NERATINIB
2.9%
of all NERATINIB reports
24
Deaths
23
Hospitalizations

How Dangerous Is Product use issue From NERATINIB?

Of the 60 reports, 24 (40.0%) resulted in death, 23 (38.3%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NERATINIB. However, 60 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 Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which NERATINIB Alternatives Have Lower Product use issue Risk?

NERATINIB vs NETARSUDIL NERATINIB vs NETUPITANT\PALONOSETRON NERATINIB vs NEULASTA NERATINIB vs NEUPOGEN NERATINIB vs NEUPRO

Related Pages

NERATINIB Full Profile All Product use issue Reports All Drugs Causing Product use issue NERATINIB Demographics