FOMEPIZOLE
Generic: FOMEPIZOLE
Mylan Institutional LLCManufacturer
INTRAVENOUSRoute
FOMEPIZOLEActive Substance
2008-03-03Original Approval
FOMEPIZOLE is FDA application ANDA078639, sponsored by MYLAN INSTITUTIONAL. 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
DRUG INEFFECTIVE
69 reports
2
TOXICITY TO VARIOUS AGENTS
50 reports
3
OVERDOSE
37 reports
4
OFF LABEL USE
33 reports
5
METABOLIC ACIDOSIS
23 reports
6
HYPOTENSION
18 reports
7
INTENTIONAL OVERDOSE
18 reports
8
HEPATOTOXICITY
17 reports
9
ACUTE KIDNEY INJURY
16 reports
10
BRAIN OEDEMA
16 reports