Does BASILIXIMAB Cause Hyperbilirubinaemia? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Hyperbilirubinaemia have been filed in association with BASILIXIMAB (Simulect). This represents 0.1% of all adverse event reports for BASILIXIMAB.
7
Reports of Hyperbilirubinaemia with BASILIXIMAB
0.1%
of all BASILIXIMAB reports
2
Deaths
6
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From BASILIXIMAB?
Of the 7 reports, 2 (28.6%) resulted in death, 6 (85.7%) required hospitalization, and 1 (14.3%) 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 BASILIXIMAB. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does BASILIXIMAB Cause?
Cytomegalovirus infection (590)
Drug ineffective (567)
Off label use (567)
Transplant rejection (554)
Kidney transplant rejection (456)
Product use in unapproved indication (428)
Pyrexia (323)
Diarrhoea (314)
Multiple organ dysfunction syndrome (298)
Polyomavirus-associated nephropathy (298)
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 BASILIXIMAB Alternatives Have Lower Hyperbilirubinaemia Risk?
BASILIXIMAB vs BAYER GENUINE ASPIRIN ORIGINAL STRENGTH
BASILIXIMAB vs BAZEDOXIFENE\ESTROGENS, CONJUGATED
BASILIXIMAB vs BCG VACCINE
BASILIXIMAB vs BEBTELOVIMAB
BASILIXIMAB vs BECLOMETHASONE