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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DEFIBROTIDE Cause Sepsis? 143 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 143 reports of Sepsis have been filed in association with DEFIBROTIDE (DEFITELIO). This represents 3.8% of all adverse event reports for DEFIBROTIDE.

143
Reports of Sepsis with DEFIBROTIDE
3.8%
of all DEFIBROTIDE reports
110
Deaths
56
Hospitalizations

How Dangerous Is Sepsis From DEFIBROTIDE?

Of the 143 reports, 110 (76.9%) resulted in death, 56 (39.2%) required hospitalization, and 19 (13.3%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

Yes, Sepsis is listed as a known adverse reaction in the official FDA drug label for DEFIBROTIDE.

What Other Side Effects Does DEFIBROTIDE Cause?

Off label use (1,323) Venoocclusive disease (576) Death (463) Multiple organ dysfunction syndrome (372) Venoocclusive liver disease (355) Intentional product use issue (201) Hypotension (169) Haemorrhage (156) Acute graft versus host disease (140) Gastrointestinal haemorrhage (125)

What Other Drugs Cause Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which DEFIBROTIDE Alternatives Have Lower Sepsis Risk?

DEFIBROTIDE vs DEFLAZACORT DEFIBROTIDE vs DEGARELIX DEFIBROTIDE vs DELAFLOXACIN MEGLUMINE DEFIBROTIDE vs DELAMANID DEFIBROTIDE vs DELANDISTROGENE MOXEPARVOVEC-ROKL

Related Pages

DEFIBROTIDE Full Profile All Sepsis Reports All Drugs Causing Sepsis DEFIBROTIDE Demographics