Does RITUXIMAB Cause Product prescribing error? 215 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 215 reports of Product prescribing error have been filed in association with RITUXIMAB (Rituxan). This represents 0.1% of all adverse event reports for RITUXIMAB.
215
Reports of Product prescribing error with RITUXIMAB
0.1%
of all RITUXIMAB reports
8
Deaths
44
Hospitalizations
How Dangerous Is Product prescribing error From RITUXIMAB?
Of the 215 reports, 8 (3.7%) resulted in death, 44 (20.5%) required hospitalization, and 6 (2.8%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB. However, 215 reports have been filed with the FAERS database.
What Other Side Effects Does RITUXIMAB Cause?
Off label use (39,751)
Drug ineffective (32,186)
Rheumatoid arthritis (19,850)
Pain (16,675)
Fatigue (15,602)
Arthralgia (12,529)
Rash (12,102)
Drug intolerance (11,876)
Infusion related reaction (11,871)
Joint swelling (11,170)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which RITUXIMAB Alternatives Have Lower Product prescribing error Risk?
RITUXIMAB vs RITUXIMAB-ABBS
RITUXIMAB vs RITUXIMAB-ARRX
RITUXIMAB vs RITUXIMAB-PVVR
RITUXIMAB vs RIVAROXABAN
RITUXIMAB vs RIVASTIGMINE