Does SUNITINIB MALATE Cause Hyperbilirubinaemia? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Hyperbilirubinaemia have been filed in association with SUNITINIB MALATE (Sunitinib malate). This represents 0.1% of all adverse event reports for SUNITINIB MALATE.
14
Reports of Hyperbilirubinaemia with SUNITINIB MALATE
0.1%
of all SUNITINIB MALATE reports
1
Deaths
8
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From SUNITINIB MALATE?
Of the 14 reports, 1 (7.1%) resulted in death, 8 (57.1%) required hospitalization, and 1 (7.1%) 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 SUNITINIB MALATE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does SUNITINIB MALATE Cause?
Death (4,385)
Diarrhoea (3,044)
Fatigue (2,865)
Nausea (2,032)
Neoplasm progression (1,920)
Disease progression (1,745)
Decreased appetite (1,676)
Asthenia (1,651)
Vomiting (1,331)
Dysgeusia (1,226)
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 SUNITINIB MALATE Alternatives Have Lower Hyperbilirubinaemia Risk?
SUNITINIB MALATE vs SUTENT
SUNITINIB MALATE vs SUTIMLIMAB-JOME
SUNITINIB MALATE vs SUVOREXANT
SUNITINIB MALATE vs SUZETRIGINE
SUNITINIB MALATE vs SYMBICORT