Does VECURONIUM Cause Wrong product administered? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Wrong product administered have been filed in association with VECURONIUM (Vecuronium Bromide). This represents 2.9% of all adverse event reports for VECURONIUM.
18
Reports of Wrong product administered with VECURONIUM
2.9%
of all VECURONIUM reports
6
Deaths
3
Hospitalizations
How Dangerous Is Wrong product administered From VECURONIUM?
Of the 18 reports, 6 (33.3%) resulted in death, 3 (16.7%) required hospitalization, and 5 (27.8%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VECURONIUM. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does VECURONIUM Cause?
Anaphylactic reaction (65)
Drug ineffective (44)
Cardiac arrest (41)
Hypotension (41)
Foetal exposure during pregnancy (28)
Neuromuscular block prolonged (25)
Rhabdomyolysis (24)
Paralysis (21)
Blood creatine phosphokinase increased (19)
Feeding intolerance (19)
What Other Drugs Cause Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which VECURONIUM Alternatives Have Lower Wrong product administered Risk?
VECURONIUM vs VEDOLIZUMAB
VECURONIUM vs VELAGLUCERASE ALFA
VECURONIUM vs VELCADE
VECURONIUM vs VELETRI
VECURONIUM vs VELIPARIB