CLEMASTINE FUMARATE
Generic: CLEMASTINE FUMARATE
Genus LifesciencesManufacturer
ORALRoute
CLEMASTINE FUMARATEActive Substance
1992-01-31Original Approval
CLEMASTINE FUMARATE is FDA application ANDA073283, sponsored by GENUS. 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
DYSPNOEA
108 reports
2
PYREXIA
103 reports
3
OFF LABEL USE
87 reports
4
NAUSEA
82 reports
5
ERYTHEMA
80 reports
6
DIARRHOEA
74 reports
7
RASH
68 reports
8
CONSTIPATION
67 reports
9
SEPSIS
64 reports
10
FATIGUE
62 reports