DAUNORUBICIN HYDROCHLORIDE
Generic: DAUNORUBICIN HYDROCHLORIDE
Meitheal Pharmaceuticals Inc.Manufacturer
INTRAVENOUSRoute
DAUNORUBICIN HYDROCHLORIDEActive Substance
2000-01-24Original Approval
DAUNORUBICIN HYDROCHLORIDE is FDA application ANDA065035, sponsored by MEITHEAL. 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
194 reports
2
MYELOSUPPRESSION
161 reports
3
BACTERIAL INFECTION
154 reports
4
SECONDARY IMMUNODEFICIENCY
130 reports
5
PYREXIA
122 reports
6
CLOSTRIDIUM DIFFICILE COLITIS
110 reports
7
OFF LABEL USE
105 reports
8
PANCYTOPENIA
92 reports
9
FUNGAL INFECTION
87 reports
10
VIRAL INFECTION
86 reports