Does TIPIRACIL\TRIFLURIDINE Cause Hyperbilirubinaemia? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Hyperbilirubinaemia have been filed in association with TIPIRACIL\TRIFLURIDINE. This represents 0.3% of all adverse event reports for TIPIRACIL\TRIFLURIDINE.
32
Reports of Hyperbilirubinaemia with TIPIRACIL\TRIFLURIDINE
0.3%
of all TIPIRACIL\TRIFLURIDINE reports
9
Deaths
15
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From TIPIRACIL\TRIFLURIDINE?
Of the 32 reports, 9 (28.1%) resulted in death, 15 (46.9%) required hospitalization, and 1 (3.1%) 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 TIPIRACIL\TRIFLURIDINE. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does TIPIRACIL\TRIFLURIDINE Cause?
Death (3,017)
Disease progression (1,774)
Fatigue (1,298)
Nausea (1,135)
Diarrhoea (965)
Decreased appetite (659)
Vomiting (628)
White blood cell count decreased (483)
Asthenia (472)
Anaemia (388)
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 TIPIRACIL\TRIFLURIDINE Alternatives Have Lower Hyperbilirubinaemia Risk?
TIPIRACIL\TRIFLURIDINE vs TIPRANAVIR
TIPIRACIL\TRIFLURIDINE vs TIRAGOLUMAB
TIPIRACIL\TRIFLURIDINE vs TIRBANIBULIN
TIPIRACIL\TRIFLURIDINE vs TIROFIBAN
TIPIRACIL\TRIFLURIDINE vs TIRZEPATIDE