DEFERASIROX
Generic: DEFERASIROX
Sun Pharmaceutical IndustriesManufacturer
ORALRoute
DEFERASIROXActive Substance
2019-11-20Original Approval
DEFERASIROX is FDA application ANDA209782, sponsored by SUN PHARM. 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.
Recalls
Top Reported Reactions
1
SICKLE CELL ANAEMIA WITH CRISIS
356 reports
2
DEATH
184 reports
3
PYREXIA
181 reports
4
DIARRHOEA
169 reports
5
OFF LABEL USE
158 reports
6
DRUG INEFFECTIVE
139 reports
7
VOMITING
129 reports
8
NAUSEA
123 reports
9
THERAPY INTERRUPTED
119 reports
10
HAEMOGLOBIN DECREASED
111 reports