Does BRINCIDOFOVIR Cause Hyperbilirubinaemia? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Hyperbilirubinaemia have been filed in association with BRINCIDOFOVIR (Tembexa). This represents 5.3% of all adverse event reports for BRINCIDOFOVIR.
5
Reports of Hyperbilirubinaemia with BRINCIDOFOVIR
5.3%
of all BRINCIDOFOVIR reports
4
Deaths
5
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From BRINCIDOFOVIR?
Of the 5 reports, 4 (80.0%) resulted in death, 5 (100.0%) required hospitalization, and 4 (80.0%) 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 BRINCIDOFOVIR. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does BRINCIDOFOVIR Cause?
Off label use (27)
Acute kidney injury (18)
Graft versus host disease in gastrointestinal tract (10)
Hypotension (9)
Pancytopenia (9)
Adenovirus infection (8)
Diarrhoea (8)
Drug resistance (8)
Multiple organ dysfunction syndrome (8)
Blood bilirubin increased (7)
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)