Does DEFIBROTIDE Cause Intentional product use issue? 201 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 201 reports of Intentional product use issue have been filed in association with DEFIBROTIDE (DEFITELIO). This represents 5.4% of all adverse event reports for DEFIBROTIDE.
201
Reports of Intentional product use issue with DEFIBROTIDE
5.4%
of all DEFIBROTIDE reports
39
Deaths
31
Hospitalizations
How Dangerous Is Intentional product use issue From DEFIBROTIDE?
Of the 201 reports, 39 (19.4%) resulted in death, 31 (15.4%) required hospitalization, and 6 (3.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEFIBROTIDE. However, 201 reports have been filed with the FAERS database.
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)
Hypotension (169)
Haemorrhage (156)
Sepsis (143)
Acute graft versus host disease (140)
Gastrointestinal haemorrhage (125)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which DEFIBROTIDE Alternatives Have Lower Intentional product use issue Risk?
DEFIBROTIDE vs DEFLAZACORT
DEFIBROTIDE vs DEGARELIX
DEFIBROTIDE vs DELAFLOXACIN MEGLUMINE
DEFIBROTIDE vs DELAMANID
DEFIBROTIDE vs DELANDISTROGENE MOXEPARVOVEC-ROKL