ETOMIDATE
Generic: ETOMIDATE INJECTION
Fosun Pharma USA IncManufacturer
INTRAVENOUSRoute
ETOMIDATEActive Substance
2017-04-18Original Approval
ETOMIDATE is FDA application ANDA209058, sponsored by GLAND. 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
RENAL FAILURE
215 reports
2
PAIN
181 reports
3
INJURY
167 reports
4
DRUG INEFFECTIVE
166 reports
5
ANXIETY
160 reports
6
HYPOTENSION
151 reports
7
UNEVALUABLE EVENT
150 reports
8
CARDIAC ARREST
143 reports
9
FEAR
136 reports
10
EMOTIONAL DISTRESS
127 reports