FLUMAZENIL
Generic: FLUMAZENIL
Fresenius Kabi USAManufacturer
INTRAVENOUSRoute
FLUMAZENILActive Substance
2004-10-12Original Approval
FLUMAZENIL is FDA application ANDA076955, 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
INTENTIONAL OVERDOSE
106 reports
2
DRUG INEFFECTIVE
91 reports
3
TOXICITY TO VARIOUS AGENTS
90 reports
4
COMA
70 reports
5
OFF LABEL USE
70 reports
6
DEPRESSED LEVEL OF CONSCIOUSNESS
64 reports
7
INTENTIONAL PRODUCT MISUSE
61 reports
8
DRUG DEPENDENCE
57 reports
9
HYPOTENSION
55 reports
10
PRODUCT USE ISSUE
55 reports