FERRIPROX
Generic: DEFERIPRONE
Chiesi USAManufacturer
ORALRoute
DEFERIPRONEActive Substance
2011-10-14Original Approval
FERRIPROX is FDA application NDA021825, sponsored by CHIESI. 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
OFF LABEL USE
1,007 reports
2
DEATH
234 reports
3
SICKLE CELL ANAEMIA WITH CRISIS
191 reports
4
AGRANULOCYTOSIS
158 reports
5
NAUSEA
158 reports
6
FATIGUE
138 reports
7
ILL-DEFINED DISORDER
135 reports
8
VOMITING
125 reports
9
NEUTROPENIA
122 reports
10
PYREXIA
120 reports