Does INFLIXIMAB-AXXQ Cause Intercepted product administration error? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Intercepted product administration error have been filed in association with INFLIXIMAB-AXXQ. This represents 5.7% of all adverse event reports for INFLIXIMAB-AXXQ.
41
Reports of Intercepted product administration error with INFLIXIMAB-AXXQ
5.7%
of all INFLIXIMAB-AXXQ reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intercepted product administration error From INFLIXIMAB-AXXQ?
Of the 41 reports.
Is Intercepted product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INFLIXIMAB-AXXQ. However, 41 reports have been filed with the FAERS database.
What Other Side Effects Does INFLIXIMAB-AXXQ Cause?
Product storage error (144)
Off label use (137)
Circumstance or information capable of leading to medication error (99)
Drug ineffective (57)
Infusion related reaction (51)
Dyspnoea (45)
Rash (43)
Fatigue (38)
Pain (38)
Headache (35)
What Other Drugs Cause Intercepted product administration error?
EVOLOCUMAB (2,508)
DENOSUMAB (1,209)
ERENUMAB-AOOE (1,015)
ETANERCEPT (574)
DARBEPOETIN ALFA (385)
PEGFILGRASTIM (356)
LEUPROLIDE (307)
ERYTHROPOIETIN (301)
ROMOSOZUMAB-AQQG (115)
BENZYL ALCOHOL\ETANERCEPT (112)
Which INFLIXIMAB-AXXQ Alternatives Have Lower Intercepted product administration error Risk?
INFLIXIMAB-AXXQ vs INFLIXIMAB-DYYB
INFLIXIMAB-AXXQ vs INFLIXIMAB-QBTX
INFLIXIMAB-AXXQ vs INFLIXIMAB, RECOMBINANT
INFLIXIMAB-AXXQ vs INFLUENZA A VIRUS A/CALIFORNIA/7/2009 LIVE ANTIGEN\INFLUENZA A VIRUS A/TEXAS/50/2012 LIVE ANTIGEN\INFLUENZA B VIRUS B/BRISBANE/60/2008 LIVE ANTIGEN\INFLUENZA B VIRUS B/MASSACHUSETTS/2/2012 LIVE ANTIGEN
INFLIXIMAB-AXXQ vs INFLUENZA VIRUS VACCINE