Does NILOTINIB Cause Product dose omission? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Product dose omission have been filed in association with NILOTINIB (nilotinib). This represents 0.2% of all adverse event reports for NILOTINIB.
52
Reports of Product dose omission with NILOTINIB
0.2%
of all NILOTINIB reports
2
Deaths
7
Hospitalizations
How Dangerous Is Product dose omission From NILOTINIB?
Of the 52 reports, 2 (3.8%) resulted in death, 7 (13.5%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NILOTINIB. However, 52 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?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which NILOTINIB Alternatives Have Lower Product dose omission Risk?
NILOTINIB vs NIMESULIDE
NILOTINIB vs NIMODIPINE
NILOTINIB vs NINTEDANIB
NILOTINIB vs NINTEDANIB ESYLATE
NILOTINIB vs NIRAPARIB