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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 Respiratory distress? 26 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Respiratory distress have been filed in association with DEFIBROTIDE (DEFITELIO). This represents 0.7% of all adverse event reports for DEFIBROTIDE.

26
Reports of Respiratory distress with DEFIBROTIDE
0.7%
of all DEFIBROTIDE reports
18
Deaths
19
Hospitalizations

How Dangerous Is Respiratory distress From DEFIBROTIDE?

Of the 26 reports, 18 (69.2%) resulted in death, 19 (73.1%) required hospitalization, and 3 (11.5%) were considered life-threatening.

Is Respiratory distress Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEFIBROTIDE. However, 26 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 Respiratory distress?

PREDNISONE (519) CYCLOPHOSPHAMIDE (496) METHOTREXATE (445) DEXAMETHASONE (431) RITUXIMAB (420) TACROLIMUS (376) ALBUTEROL (355) TREPROSTINIL (345) VINCRISTINE (342) PREDNISOLONE (298)

Which DEFIBROTIDE Alternatives Have Lower Respiratory distress 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 Respiratory distress Reports All Drugs Causing Respiratory distress DEFIBROTIDE Demographics