Does RITUXIMAB Cause Unevaluable event? 303 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 303 reports of Unevaluable event have been filed in association with RITUXIMAB (Rituxan). This represents 0.2% of all adverse event reports for RITUXIMAB.
303
Reports of Unevaluable event with RITUXIMAB
0.2%
of all RITUXIMAB reports
30
Deaths
114
Hospitalizations
How Dangerous Is Unevaluable event From RITUXIMAB?
Of the 303 reports, 30 (9.9%) resulted in death, 114 (37.6%) required hospitalization, and 13 (4.3%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB. However, 303 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which RITUXIMAB Alternatives Have Lower Unevaluable event Risk?
RITUXIMAB vs RITUXIMAB-ABBS
RITUXIMAB vs RITUXIMAB-ARRX
RITUXIMAB vs RITUXIMAB-PVVR
RITUXIMAB vs RIVAROXABAN
RITUXIMAB vs RIVASTIGMINE