VECURONIUM BROMIDE
Generic: VECURONIUM BROMIDE
Sun Pharmaceutical IndustriesManufacturer
INTRAVENOUSRoute
VECURONIUM BROMIDEActive Substance
2009-06-17Original Approval
VECURONIUM BROMIDE is FDA application ANDA079001, sponsored by SUN PHARM. 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.
Recalls
Class I2019-01-03
Vecuronium Bromide for Injection 10 mg*, *1mg/mL when reconstituted to 10 mL Lyophilized, 10 x 10 mg vials, Rx only, ManPresence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide f
Class I2019-01-03
Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to 20 mL Lyophilized, 10 x 20 mg vials, Rx Only, ManuPresence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide f
Top Reported Reactions
1
RENAL FAILURE
134 reports
2
HYPOTENSION
124 reports
3
PAIN
122 reports
4
CARDIAC ARREST
109 reports
5
INJURY
105 reports
6
UNEVALUABLE EVENT
102 reports
7
ANXIETY
101 reports
8
RENAL IMPAIRMENT
95 reports
9
FEAR
94 reports
10
BRADYCARDIA
93 reports