Does ROCURONIUM Cause Type i hypersensitivity? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Type i hypersensitivity have been filed in association with ROCURONIUM (ROCURONIUM BROMIDE). This represents 0.5% of all adverse event reports for ROCURONIUM.
31
Reports of Type i hypersensitivity with ROCURONIUM
0.5%
of all ROCURONIUM reports
0
Deaths
16
Hospitalizations
How Dangerous Is Type i hypersensitivity From ROCURONIUM?
Of the 31 reports, 16 (51.6%) required hospitalization, and 14 (45.2%) were considered life-threatening.
Is Type i hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROCURONIUM. However, 31 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 Type i hypersensitivity?
OXALIPLATIN (266)
AMOXICILLIN (260)
LEVOFLOXACIN (180)
ACETAMINOPHEN (129)
CARBOPLATIN (125)
DICLOFENAC (111)
PANTOPRAZOLE (110)
PACLITAXEL (107)
IBUPROFEN (103)
OMEPRAZOLE (98)
Which ROCURONIUM Alternatives Have Lower Type i hypersensitivity Risk?
ROCURONIUM vs ROFECOXIB
ROCURONIUM vs ROFLUMILAST
ROCURONIUM vs ROLAPITANT
ROCURONIUM vs ROMIDEPSIN
ROCURONIUM vs ROMIPLOSTIM