MESNA

Generic: MESNA

Fresenius Kabi USAManufacturer
INTRAVENOUSRoute
MESNAActive Substance
2001-04-26Original Approval

MESNA is FDA application ANDA075811, 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
FEBRILE NEUTROPENIA
1,274 reports
2
PYREXIA
681 reports
3
OFF LABEL USE
647 reports
4
NEUTROPENIA
574 reports
5
THROMBOCYTOPENIA
396 reports
6
ANAEMIA
390 reports
7
VOMITING
378 reports
8
PANCYTOPENIA
365 reports
9
NAUSEA
363 reports
10
SEPSIS
358 reports