Does ROCURONIUM Cause Product administration error? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Product administration error have been filed in association with ROCURONIUM (ROCURONIUM BROMIDE). This represents 0.5% of all adverse event reports for ROCURONIUM.
30
Reports of Product administration error with ROCURONIUM
0.5%
of all ROCURONIUM reports
5
Deaths
12
Hospitalizations
How Dangerous Is Product administration error From ROCURONIUM?
Of the 30 reports, 5 (16.7%) resulted in death, 12 (40.0%) required hospitalization, and 14 (46.7%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROCURONIUM. However, 30 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which ROCURONIUM Alternatives Have Lower Product administration error Risk?
ROCURONIUM vs ROFECOXIB
ROCURONIUM vs ROFLUMILAST
ROCURONIUM vs ROLAPITANT
ROCURONIUM vs ROMIDEPSIN
ROCURONIUM vs ROMIPLOSTIM