IFOSFAMIDE
Generic: IFOSFAMIDE
Fresenius Kabi USAManufacturer
INTRAVENOUSRoute
IFOSFAMIDEActive Substance
2002-05-28Original Approval
IFOSFAMIDE is FDA application ANDA076078, sponsored by FRESENIUS KABI USA. 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
2,758 reports
2
FEBRILE NEUTROPENIA
2,703 reports
3
DISEASE PROGRESSION
2,061 reports
4
NEUTROPENIA
1,884 reports
5
DRUG INEFFECTIVE
1,592 reports
6
THROMBOCYTOPENIA
1,540 reports
7
ANAEMIA
1,255 reports
8
PYREXIA
998 reports
9
PRODUCT USE IN UNAPPROVED INDICATION
891 reports
10
SEPSIS
809 reports