Does NILOTINIB Cause Product dose omission issue? 219 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 219 reports of Product dose omission issue have been filed in association with NILOTINIB (nilotinib). This represents 1.0% of all adverse event reports for NILOTINIB.
219
Reports of Product dose omission issue with NILOTINIB
1.0%
of all NILOTINIB reports
6
Deaths
40
Hospitalizations
How Dangerous Is Product dose omission issue From NILOTINIB?
Of the 219 reports, 6 (2.7%) resulted in death, 40 (18.3%) required hospitalization, and 4 (1.8%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NILOTINIB. However, 219 reports have been filed with the FAERS database.
What Other Side Effects Does NILOTINIB Cause?
Death (2,667)
Fatigue (1,679)
Rash (1,250)
Nausea (1,180)
Headache (1,177)
Pain (1,169)
Dyspnoea (1,070)
Diarrhoea (998)
Drug ineffective (992)
Malaise (961)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which NILOTINIB Alternatives Have Lower Product dose omission issue Risk?
NILOTINIB vs NIMESULIDE
NILOTINIB vs NIMODIPINE
NILOTINIB vs NINTEDANIB
NILOTINIB vs NINTEDANIB ESYLATE
NILOTINIB vs NIRAPARIB