Does TEMOZOLOMIDE Cause Hyperbilirubinaemia? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Hyperbilirubinaemia have been filed in association with TEMOZOLOMIDE (TEMOZOLOMIDE). This represents 0.1% of all adverse event reports for TEMOZOLOMIDE.
18
Reports of Hyperbilirubinaemia with TEMOZOLOMIDE
0.1%
of all TEMOZOLOMIDE reports
1
Deaths
9
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From TEMOZOLOMIDE?
Of the 18 reports, 1 (5.6%) resulted in death, 9 (50.0%) required hospitalization, and 1 (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 TEMOZOLOMIDE. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does TEMOZOLOMIDE Cause?
Disease progression (1,562)
Death (1,403)
Off label use (1,357)
Product use in unapproved indication (1,353)
Thrombocytopenia (1,300)
Drug ineffective (1,131)
Nausea (1,071)
Neutropenia (809)
Malignant neoplasm progression (779)
Fatigue (766)
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 TEMOZOLOMIDE Alternatives Have Lower Hyperbilirubinaemia Risk?
TEMOZOLOMIDE vs TEMSIROLIMUS
TEMOZOLOMIDE vs TENAMFETAMINE
TEMOZOLOMIDE vs TENAPANOR
TEMOZOLOMIDE vs TENECTEPLASE
TEMOZOLOMIDE vs TENELIGLIPTIN