SUGAMMADEX
Generic: SUGAMMADEX SODIUM, SUGAMMADEX
Solupharm Pharmazeutische Erzeugnisse GmbHManufacturer
INTRAVENOUSRoute
SUGAMMADEX SODIUMActive Substance
2026-07-28Original Approval
SUGAMMADEX is FDA application ANDA215260, sponsored by TAMARANG. 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
ANAPHYLACTIC REACTION
156 reports
2
DRUG INEFFECTIVE
86 reports
3
BRADYCARDIA
80 reports
4
HYPOTENSION
75 reports
5
DRUG INTERACTION
69 reports
6
ANAPHYLACTIC SHOCK
68 reports
7
CARDIAC ARREST
62 reports
8
BRONCHOSPASM
53 reports
9
RECURRENCE OF NEUROMUSCULAR BLOCKADE
40 reports
10
TACHYCARDIA
37 reports