Does CAPECITABINE Cause Hyperbilirubinaemia? 279 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 279 reports of Hyperbilirubinaemia have been filed in association with CAPECITABINE (Capecitabine). This represents 0.4% of all adverse event reports for CAPECITABINE.
279
Reports of Hyperbilirubinaemia with CAPECITABINE
0.4%
of all CAPECITABINE reports
18
Deaths
77
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From CAPECITABINE?
Of the 279 reports, 18 (6.5%) resulted in death, 77 (27.6%) required hospitalization, and 10 (3.6%) 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 CAPECITABINE. However, 279 reports have been filed with the FAERS database.
What Other Side Effects Does CAPECITABINE Cause?
Diarrhoea (9,277)
Nausea (6,248)
Palmar-plantar erythrodysaesthesia syndrome (5,294)
Fatigue (5,018)
Death (4,422)
Vomiting (4,111)
Disease progression (3,808)
Off label use (3,193)
Malignant neoplasm progression (2,425)
Asthenia (2,352)
What Other Drugs Cause Hyperbilirubinaemia?
METHOTREXATE (603)
RIBAVIRIN (560)
VINCRISTINE (479)
CYTARABINE (397)
PEGASPARGASE (349)
ACETAMINOPHEN (330)
CYCLOPHOSPHAMIDE (330)
DEXAMETHASONE (315)
SOFOSBUVIR (260)
PREDNISONE (259)
Which CAPECITABINE Alternatives Have Lower Hyperbilirubinaemia Risk?
CAPECITABINE vs CAPIVASERTIB
CAPECITABINE vs CAPLACIZUMAB
CAPECITABINE vs CAPLACIZUMAB-YHDP
CAPECITABINE vs CAPMATINIB
CAPECITABINE vs CAPREOMYCIN