Does RITUXIMAB-ARRX Cause Intercepted product preparation error? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Intercepted product preparation error have been filed in association with RITUXIMAB-ARRX. This represents 4.6% of all adverse event reports for RITUXIMAB-ARRX.
16
Reports of Intercepted product preparation error with RITUXIMAB-ARRX
4.6%
of all RITUXIMAB-ARRX reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intercepted product preparation error From RITUXIMAB-ARRX?
Of the 16 reports.
Is Intercepted product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-ARRX. However, 16 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)
Intercepted product administration error (51)
Accidental exposure to product (17)
Fatigue (14)
Infusion related reaction (14)
Drug ineffective (12)
Dyspnoea (12)
Malaise (12)
What Other Drugs Cause Intercepted product preparation error?
LEUPROLIDE (8,621)
PEGFILGRASTIM (1,514)
DEVICE (1,033)
CARFILZOMIB (367)
BLINATUMOMAB (110)
BEVACIZUMAB-AWWB (54)
ROMIPLOSTIM (48)
TRASTUZUMAB-ANNS (42)
AFLIBERCEPT (39)
TOCILIZUMAB (26)
Which RITUXIMAB-ARRX Alternatives Have Lower Intercepted product preparation error Risk?
RITUXIMAB-ARRX vs RITUXIMAB-PVVR
RITUXIMAB-ARRX vs RIVAROXABAN
RITUXIMAB-ARRX vs RIVASTIGMINE
RITUXIMAB-ARRX vs RIVOTRIL
RITUXIMAB-ARRX vs RIZATRIPTAN