Does THIOTEPA Cause Hyperbilirubinaemia? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Hyperbilirubinaemia have been filed in association with THIOTEPA (Thiotepa). This represents 0.5% of all adverse event reports for THIOTEPA.
36
Reports of Hyperbilirubinaemia with THIOTEPA
0.5%
of all THIOTEPA reports
15
Deaths
21
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From THIOTEPA?
Of the 36 reports, 15 (41.7%) resulted in death, 21 (58.3%) required hospitalization, and 2 (5.6%) 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 THIOTEPA. However, 36 reports have been filed with the FAERS database.
What Other Side Effects Does THIOTEPA Cause?
Off label use (762)
Febrile neutropenia (645)
Mucosal inflammation (616)
Cytomegalovirus infection (446)
Product use in unapproved indication (425)
Pyrexia (359)
Drug ineffective (358)
Acute graft versus host disease in skin (355)
Acute graft versus host disease (331)
Cytomegalovirus infection reactivation (325)
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 THIOTEPA Alternatives Have Lower Hyperbilirubinaemia Risk?
THIOTEPA vs THIOTHIXENE
THIOTEPA vs THROMBIN
THIOTEPA vs THROMBIN HUMAN
THIOTEPA vs THYMOCYTE IMMUNE GLOBULIN NOS
THIOTEPA vs THYMOGLOBULINE