Does IFOSFAMIDE Cause Hyperbilirubinaemia? 48 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 48 reports of Hyperbilirubinaemia have been filed in association with IFOSFAMIDE (IFEX). This represents 0.3% of all adverse event reports for IFOSFAMIDE.
48
Reports of Hyperbilirubinaemia with IFOSFAMIDE
0.3%
of all IFOSFAMIDE reports
16
Deaths
18
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From IFOSFAMIDE?
Of the 48 reports, 16 (33.3%) resulted in death, 18 (37.5%) required hospitalization, and 1 (2.1%) were considered life-threatening.
Is Hyperbilirubinaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IFOSFAMIDE. However, 48 reports have been filed with the FAERS database.
What Other Side Effects Does IFOSFAMIDE Cause?
Off label use (2,281)
Febrile neutropenia (2,225)
Disease progression (1,912)
Neutropenia (1,509)
Drug ineffective (1,331)
Thrombocytopenia (1,227)
Anaemia (1,067)
Product use in unapproved indication (890)
Pyrexia (752)
Sepsis (712)
What Other Drugs Cause Hyperbilirubinaemia?
METHOTREXATE (603)
RIBAVIRIN (560)
VINCRISTINE (479)
CYTARABINE (397)
PEGASPARGASE (349)
ACETAMINOPHEN (330)
CYCLOPHOSPHAMIDE (330)
DEXAMETHASONE (315)
CAPECITABINE (279)
SOFOSBUVIR (260)
Which IFOSFAMIDE Alternatives Have Lower Hyperbilirubinaemia Risk?
IFOSFAMIDE vs IGURATIMOD
IFOSFAMIDE vs ILOPERIDONE
IFOSFAMIDE vs ILOPROST
IFOSFAMIDE vs IMATINIB
IFOSFAMIDE vs IMBRUVICA