ROCURONIUM BROMIDE

Generic: ROCURONIUM BROMIDE

Shandong New Time Pharmaceutical Co.Manufacturer
INTRAVENOUSRoute
ROCURONIUM BROMIDEActive Substance
2024-07-12Original Approval

ROCURONIUM BROMIDE is FDA application ANDA215684, sponsored by SHANDONG. 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 II2024-02-07
Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx only, Mfg: Auromedics Pharma L

cGMP Deviations: Products were stored outside the drug label specifications.

Top Reported Reactions

1
ANAPHYLACTIC SHOCK
655 reports
2
DRUG INEFFECTIVE
654 reports
3
ANAPHYLACTIC REACTION
594 reports
4
HYPOTENSION
506 reports
5
CARDIAC ARREST
346 reports
6
TACHYCARDIA
214 reports
7
BRONCHOSPASM
208 reports
8
BRADYCARDIA
195 reports
9
RASH
180 reports
10
DRUG INTERACTION
164 reports