Does RITUXIMAB-ARRX Cause Intercepted product administration error? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Intercepted product administration error have been filed in association with RITUXIMAB-ARRX. This represents 14.7% of all adverse event reports for RITUXIMAB-ARRX.
51
Reports of Intercepted product administration error with RITUXIMAB-ARRX
14.7%
of all RITUXIMAB-ARRX reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intercepted product administration error From RITUXIMAB-ARRX?
Of the 51 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 RITUXIMAB-ARRX. However, 51 reports have been filed with the FAERS database.
What Other Side Effects Does RITUXIMAB-ARRX Cause?
Product storage error (165)
Circumstance or information capable of leading to medication error (116)
Off label use (56)
Accidental exposure to product (17)
Intercepted product preparation error (16)
Fatigue (14)
Infusion related reaction (14)
Drug ineffective (12)
Dyspnoea (12)
Malaise (12)
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 RITUXIMAB-ARRX Alternatives Have Lower Intercepted product administration error Risk?
RITUXIMAB-ARRX vs RITUXIMAB-PVVR
RITUXIMAB-ARRX vs RIVAROXABAN
RITUXIMAB-ARRX vs RIVASTIGMINE
RITUXIMAB-ARRX vs RIVOTRIL
RITUXIMAB-ARRX vs RIZATRIPTAN