HELIUM
Generic: HELIUM
NexAirManufacturer
RESPIRATORY (INHALATION)Route
HELIUMActive Substance
2016-02-20Original Approval
HELIUM is FDA application NDA209033, sponsored by NEXAIR LLC. 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
COMPLETED SUICIDE
23 reports
2
ASPHYXIA
6 reports
3
OVERDOSE
6 reports
4
TOXICITY TO VARIOUS AGENTS
5 reports
5
GENERALISED TONIC-CLONIC SEIZURE
4 reports
6
SEDATION
4 reports
7
DRUG INEFFECTIVE
3 reports
8
DRUG LEVEL INCREASED
3 reports
9
MYALGIA
3 reports
10
OFF LABEL USE
3 reports