NILOTINIB

Generic: NILOTINIB

Dr. Reddy's Laboratories IncManufacturer
ORALRoute
NILOTINIB HYDROCHLORIDE MONOHYDRATEActive Substance
2025-11-19Original Approval

NILOTINIB is FDA application ANDA218350, sponsored by DR REDDYS. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.

Top Reported Reactions

1
DRUG INTOLERANCE
412 reports
2
DRUG INEFFECTIVE
344 reports
3
DRUG RESISTANCE
340 reports
4
DIARRHOEA
329 reports
5
DYSPNOEA
328 reports
6
FATIGUE
316 reports
7
NAUSEA
298 reports
8
HEADACHE
297 reports
9
MYALGIA
279 reports
10
ARTHRALGIA
269 reports