Does NILOTINIB Cause Incorrect product administration duration? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Incorrect product administration duration have been filed in association with NILOTINIB (nilotinib). This represents 0.0% of all adverse event reports for NILOTINIB.
6
Reports of Incorrect product administration duration with NILOTINIB
0.0%
of all NILOTINIB reports
1
Deaths
3
Hospitalizations
How Dangerous Is Incorrect product administration duration From NILOTINIB?
Of the 6 reports, 1 (16.7%) resulted in death, 3 (50.0%) required hospitalization, and 2 (33.3%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NILOTINIB. However, 6 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which NILOTINIB Alternatives Have Lower Incorrect product administration duration Risk?
NILOTINIB vs NIMESULIDE
NILOTINIB vs NIMODIPINE
NILOTINIB vs NINTEDANIB
NILOTINIB vs NINTEDANIB ESYLATE
NILOTINIB vs NIRAPARIB