Does FLUDARABINE Cause Device related sepsis? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Device related sepsis have been filed in association with FLUDARABINE (Fludarabine Phosphate). This represents 0.1% of all adverse event reports for FLUDARABINE.
31
Reports of Device related sepsis with FLUDARABINE
0.1%
of all FLUDARABINE reports
7
Deaths
8
Hospitalizations
How Dangerous Is Device related sepsis From FLUDARABINE?
Of the 31 reports, 7 (22.6%) resulted in death, 8 (25.8%) required hospitalization.
Is Device related sepsis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUDARABINE. However, 31 reports have been filed with the FAERS database.
What Other Side Effects Does FLUDARABINE Cause?
Off label use (3,018)
Febrile neutropenia (2,055)
Drug ineffective (1,630)
Pyrexia (1,606)
Product use in unapproved indication (1,530)
Cytokine release syndrome (1,458)
Neutropenia (1,175)
Cytomegalovirus infection (1,132)
Mucosal inflammation (1,036)
Sepsis (981)
What Other Drugs Cause Device related sepsis?
TEDUGLUTIDE (226)
TREPROSTINIL (225)
CYCLOPHOSPHAMIDE (130)
RITUXIMAB (113)
EPOPROSTENOL (89)
CYCLOSPORINE (82)
METHYLPREDNISOLONE (82)
BORTEZOMIB (79)
MACITENTAN (55)
DEXAMETHASONE (53)
Which FLUDARABINE Alternatives Have Lower Device related sepsis Risk?
FLUDARABINE vs FLUDEOXYGLUCOSE F-18
FLUDARABINE vs FLUDROCORTISONE
FLUDARABINE vs FLUINDIONE
FLUDARABINE vs FLUMAZENIL
FLUDARABINE vs FLUMETHASONE