Does RITUXIMAB Cause Device related sepsis? 113 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 113 reports of Device related sepsis have been filed in association with RITUXIMAB (Rituxan). This represents 0.1% of all adverse event reports for RITUXIMAB.
113
Reports of Device related sepsis with RITUXIMAB
0.1%
of all RITUXIMAB reports
19
Deaths
41
Hospitalizations
How Dangerous Is Device related sepsis From RITUXIMAB?
Of the 113 reports, 19 (16.8%) resulted in death, 41 (36.3%) required hospitalization, and 29 (25.7%) were considered life-threatening.
Is Device related sepsis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB. However, 113 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 Device related sepsis?
TEDUGLUTIDE (226)
TREPROSTINIL (225)
CYCLOPHOSPHAMIDE (130)
EPOPROSTENOL (89)
CYCLOSPORINE (82)
METHYLPREDNISOLONE (82)
BORTEZOMIB (79)
MACITENTAN (55)
DEXAMETHASONE (53)
ADALIMUMAB (49)
Which RITUXIMAB Alternatives Have Lower Device related sepsis Risk?
RITUXIMAB vs RITUXIMAB-ABBS
RITUXIMAB vs RITUXIMAB-ARRX
RITUXIMAB vs RITUXIMAB-PVVR
RITUXIMAB vs RIVAROXABAN
RITUXIMAB vs RIVASTIGMINE