DEXRAZOXANE
Generic: DEXRAZOXANE
Hikma Pharmaceuticals USA Inc.Manufacturer
INTRAVENOUSRoute
DEXRAZOXANE HYDROCHLORIDEActive Substance
2004-09-28Original Approval
DEXRAZOXANE is FDA application ANDA076068, sponsored by HIKMA. 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
FEBRILE NEUTROPENIA
141 reports
2
OFF LABEL USE
128 reports
3
NEUTROPENIA
104 reports
4
PRODUCT USE ISSUE
55 reports
5
PYREXIA
54 reports
6
MYELOSUPPRESSION
43 reports
7
NAUSEA
43 reports
8
WHITE BLOOD CELL COUNT DECREASED
39 reports
9
ANAEMIA
37 reports
10
VOMITING
37 reports