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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 Post procedural haemorrhage? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Post procedural haemorrhage have been filed in association with DEFIBROTIDE (DEFITELIO). This represents 0.4% of all adverse event reports for DEFIBROTIDE.

14
Reports of Post procedural haemorrhage with DEFIBROTIDE
0.4%
of all DEFIBROTIDE reports
3
Deaths
1
Hospitalizations

How Dangerous Is Post procedural haemorrhage From DEFIBROTIDE?

Of the 14 reports, 3 (21.4%) resulted in death, 1 (7.1%) required hospitalization, and 2 (14.3%) were considered life-threatening.

Is Post procedural haemorrhage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEFIBROTIDE. However, 14 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) Intentional product use issue (201) Hypotension (169) Haemorrhage (156) Sepsis (143) Acute graft versus host disease (140)

What Other Drugs Cause Post procedural haemorrhage?

LEVONORGESTREL (1,106) RIVAROXABAN (930) ASPIRIN (618) APIXABAN (539) ADALIMUMAB (476) IBRUTINIB (269) CLOPIDOGREL BISULFATE (235) HEPARIN (174) WARFARIN (170) DABIGATRAN ETEXILATE (121)

Which DEFIBROTIDE Alternatives Have Lower Post procedural haemorrhage 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 Post procedural haemorrhage Reports All Drugs Causing Post procedural haemorrhage DEFIBROTIDE Demographics