Does REGORAFENIB Cause Hyperbilirubinaemia? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Hyperbilirubinaemia have been filed in association with REGORAFENIB (Stivarga). This represents 0.6% of all adverse event reports for REGORAFENIB.
52
Reports of Hyperbilirubinaemia with REGORAFENIB
0.6%
of all REGORAFENIB reports
16
Deaths
25
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From REGORAFENIB?
Of the 52 reports, 16 (30.8%) resulted in death, 25 (48.1%) required hospitalization, and 5 (9.6%) 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 REGORAFENIB. However, 52 reports have been filed with the FAERS database.
What Other Side Effects Does REGORAFENIB Cause?
Off label use (1,906)
Fatigue (1,530)
Palmar-plantar erythrodysaesthesia syndrome (1,230)
Diarrhoea (1,221)
Decreased appetite (941)
Asthenia (825)
Death (813)
Dysphonia (702)
Nausea (688)
Pain in extremity (686)
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 REGORAFENIB Alternatives Have Lower Hyperbilirubinaemia Risk?
REGORAFENIB vs REGORAFENIB\REGORAFENIB
REGORAFENIB vs RELATLIMAB
REGORAFENIB vs RELPAX
REGORAFENIB vs RELUGOLIX
REGORAFENIB vs REMDESIVIR