PALONOSETRON
Generic: PALONOSETRON
Fresenius Kabi USAManufacturer
INTRAVENOUSRoute
PALONOSETRON HYDROCHLORIDEActive Substance
2018-09-19Original Approval
PALONOSETRON is FDA application ANDA206802, 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
NAUSEA
597 reports
2
DIARRHOEA
366 reports
3
VOMITING
356 reports
4
FEBRILE NEUTROPENIA
338 reports
5
FATIGUE
337 reports
6
OFF LABEL USE
334 reports
7
NEUTROPENIA
323 reports
8
ANAEMIA
312 reports
9
PYREXIA
283 reports
10
ALOPECIA
278 reports