Does RITUXIMAB Cause Condition aggravated? 8,627 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8,627 reports of Condition aggravated have been filed in association with RITUXIMAB (Rituxan). This represents 4.8% of all adverse event reports for RITUXIMAB.
8,627
Reports of Condition aggravated with RITUXIMAB
4.8%
of all RITUXIMAB reports
2,088
Deaths
3,654
Hospitalizations
How Dangerous Is Condition aggravated From RITUXIMAB?
Of the 8,627 reports, 2,088 (24.2%) resulted in death, 3,654 (42.4%) required hospitalization, and 2,116 (24.5%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB. However, 8,627 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
TOCILIZUMAB (8,471)
Which RITUXIMAB Alternatives Have Lower Condition aggravated Risk?
RITUXIMAB vs RITUXIMAB-ABBS
RITUXIMAB vs RITUXIMAB-ARRX
RITUXIMAB vs RITUXIMAB-PVVR
RITUXIMAB vs RIVAROXABAN
RITUXIMAB vs RIVASTIGMINE