Does GILTERITINIB Cause Hyperbilirubinaemia? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Hyperbilirubinaemia have been filed in association with GILTERITINIB (Xospata). This represents 0.3% of all adverse event reports for GILTERITINIB.
9
Reports of Hyperbilirubinaemia with GILTERITINIB
0.3%
of all GILTERITINIB reports
1
Deaths
6
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From GILTERITINIB?
Of the 9 reports, 1 (11.1%) resulted in death, 6 (66.7%) required hospitalization, and 2 (22.2%) 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 GILTERITINIB. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does GILTERITINIB Cause?
Acute myeloid leukaemia (366)
Febrile neutropenia (346)
Off label use (334)
Platelet count decreased (327)
Pneumonia (302)
Myelosuppression (300)
Pyrexia (281)
Death (206)
Product use issue (189)
Hepatic function abnormal (181)
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 GILTERITINIB Alternatives Have Lower Hyperbilirubinaemia Risk?
GILTERITINIB vs GIMERACIL\OTERACIL\TEGAFUR
GILTERITINIB vs GINKGO
GILTERITINIB vs GIVINOSTAT
GILTERITINIB vs GIVOSIRAN
GILTERITINIB vs GLASDEGIB