Does DEFIBROTIDE Cause Incorrect drug administration duration? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Incorrect drug administration duration have been filed in association with DEFIBROTIDE (DEFITELIO). This represents 0.3% of all adverse event reports for DEFIBROTIDE.
10
Reports of Incorrect drug administration duration with DEFIBROTIDE
0.3%
of all DEFIBROTIDE reports
6
Deaths
3
Hospitalizations
How Dangerous Is Incorrect drug administration duration From DEFIBROTIDE?
Of the 10 reports, 6 (60.0%) resulted in death, 3 (30.0%) required hospitalization, and 1 (10.0%) were considered life-threatening.
Is Incorrect drug administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEFIBROTIDE. However, 10 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 Incorrect drug administration duration?
ETONOGESTREL (1,796)
POLYETHYLENE GLYCOL 3350 (1,722)
NAPROXEN (1,272)
DOCOSANOL (803)
ETHINYL ESTRADIOL\ETONOGESTREL (740)
NICOTINE (561)
RANITIDINE (504)
GUAIFENESIN (490)
INSULIN LISPRO (367)
ACETAMINOPHEN (340)
Which DEFIBROTIDE Alternatives Have Lower Incorrect drug administration duration Risk?
DEFIBROTIDE vs DEFLAZACORT
DEFIBROTIDE vs DEGARELIX
DEFIBROTIDE vs DELAFLOXACIN MEGLUMINE
DEFIBROTIDE vs DELAMANID
DEFIBROTIDE vs DELANDISTROGENE MOXEPARVOVEC-ROKL