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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 Hypersensitivity? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Hypersensitivity have been filed in association with DEFIBROTIDE (DEFITELIO). This represents 0.3% of all adverse event reports for DEFIBROTIDE.

11
Reports of Hypersensitivity with DEFIBROTIDE
0.3%
of all DEFIBROTIDE reports
0
Deaths
10
Hospitalizations

How Dangerous Is Hypersensitivity From DEFIBROTIDE?

Of the 11 reports, 10 (90.9%) required hospitalization.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity 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) Sepsis (143) Acute graft versus host disease (140)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which DEFIBROTIDE Alternatives Have Lower Hypersensitivity 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 Hypersensitivity Reports All Drugs Causing Hypersensitivity DEFIBROTIDE Demographics