Does NERATINIB Cause Product prescribing error? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product prescribing error have been filed in association with NERATINIB. This represents 0.6% of all adverse event reports for NERATINIB.
13
Reports of Product prescribing error with NERATINIB
0.6%
of all NERATINIB reports
2
Deaths
3
Hospitalizations
How Dangerous Is Product prescribing error From NERATINIB?
Of the 13 reports, 2 (15.4%) resulted in death, 3 (23.1%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NERATINIB. However, 13 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which NERATINIB Alternatives Have Lower Product prescribing error Risk?
NERATINIB vs NETARSUDIL
NERATINIB vs NETUPITANT\PALONOSETRON
NERATINIB vs NEULASTA
NERATINIB vs NEUPOGEN
NERATINIB vs NEUPRO