Does CASIRIVIMAB\IMDEVIMAB Cause Product administration error? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Product administration error have been filed in association with CASIRIVIMAB\IMDEVIMAB. This represents 0.6% of all adverse event reports for CASIRIVIMAB\IMDEVIMAB.
25
Reports of Product administration error with CASIRIVIMAB\IMDEVIMAB
0.6%
of all CASIRIVIMAB\IMDEVIMAB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From CASIRIVIMAB\IMDEVIMAB?
Of the 25 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CASIRIVIMAB\IMDEVIMAB. However, 25 reports have been filed with the FAERS database.
What Other Side Effects Does CASIRIVIMAB\IMDEVIMAB Cause?
Infusion related reaction (875)
Dyspnoea (687)
Nausea (416)
Oxygen saturation decreased (390)
Dizziness (357)
Pyrexia (306)
Chest discomfort (294)
Chills (265)
Flushing (238)
Cough (235)
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 CASIRIVIMAB\IMDEVIMAB Alternatives Have Lower Product administration error Risk?
CASIRIVIMAB\IMDEVIMAB vs CASPOFUNGIN
CASIRIVIMAB\IMDEVIMAB vs CATEQUENTINIB
CASIRIVIMAB\IMDEVIMAB vs CC-4047
CASIRIVIMAB\IMDEVIMAB vs CEDAZURIDINE\DECITABINE
CASIRIVIMAB\IMDEVIMAB vs CEDIRANIB