Does ROCURONIUM Cause Wrong product administered? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Wrong product administered have been filed in association with ROCURONIUM (ROCURONIUM BROMIDE). This represents 0.4% of all adverse event reports for ROCURONIUM.
28
Reports of Wrong product administered with ROCURONIUM
0.4%
of all ROCURONIUM reports
4
Deaths
6
Hospitalizations
How Dangerous Is Wrong product administered From ROCURONIUM?
Of the 28 reports, 4 (14.3%) resulted in death, 6 (21.4%) required hospitalization, and 8 (28.6%) 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 ROCURONIUM. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does ROCURONIUM Cause?
Anaphylactic reaction (971)
Anaphylactic shock (897)
Drug ineffective (818)
Hypotension (636)
Cardiac arrest (388)
Tachycardia (262)
Bronchospasm (252)
Urticaria (240)
Rash (237)
Bradycardia (231)
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 ROCURONIUM Alternatives Have Lower Wrong product administered Risk?
ROCURONIUM vs ROFECOXIB
ROCURONIUM vs ROFLUMILAST
ROCURONIUM vs ROLAPITANT
ROCURONIUM vs ROMIDEPSIN
ROCURONIUM vs ROMIPLOSTIM