Does FLUDARABINE Cause Product administration error? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Product administration error have been filed in association with FLUDARABINE (Fludarabine Phosphate). This represents 0.1% of all adverse event reports for FLUDARABINE.
20
Reports of Product administration error with FLUDARABINE
0.1%
of all FLUDARABINE reports
15
Deaths
14
Hospitalizations
How Dangerous Is Product administration error From FLUDARABINE?
Of the 20 reports, 15 (75.0%) resulted in death, 14 (70.0%) required hospitalization, and 8 (40.0%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUDARABINE. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does FLUDARABINE Cause?
Off label use (3,018)
Febrile neutropenia (2,055)
Drug ineffective (1,630)
Pyrexia (1,606)
Product use in unapproved indication (1,530)
Cytokine release syndrome (1,458)
Neutropenia (1,175)
Cytomegalovirus infection (1,132)
Mucosal inflammation (1,036)
Sepsis (981)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which FLUDARABINE Alternatives Have Lower Product administration error Risk?
FLUDARABINE vs FLUDEOXYGLUCOSE F-18
FLUDARABINE vs FLUDROCORTISONE
FLUDARABINE vs FLUINDIONE
FLUDARABINE vs FLUMAZENIL
FLUDARABINE vs FLUMETHASONE