Does APALUTAMIDE Cause Hepatic function abnormal? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Hepatic function abnormal have been filed in association with APALUTAMIDE (ERLEADA). This represents 0.3% of all adverse event reports for APALUTAMIDE.
32
Reports of Hepatic function abnormal with APALUTAMIDE
0.3%
of all APALUTAMIDE reports
4
Deaths
14
Hospitalizations
How Dangerous Is Hepatic function abnormal From APALUTAMIDE?
Of the 32 reports, 4 (12.5%) resulted in death, 14 (43.8%) required hospitalization, and 1 (3.1%) were considered life-threatening.
Is Hepatic function abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APALUTAMIDE. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does APALUTAMIDE Cause?
Rash (1,117)
Death (1,008)
Fatigue (824)
Hot flush (532)
Product dose omission issue (384)
Diarrhoea (317)
Asthenia (303)
Dizziness (294)
Fall (268)
Off label use (257)
What Other Drugs Cause Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which APALUTAMIDE Alternatives Have Lower Hepatic function abnormal Risk?
APALUTAMIDE vs APATINIB
APALUTAMIDE vs APIDRA
APALUTAMIDE vs APIDRA SOLOSTAR
APALUTAMIDE vs APIXABAN
APALUTAMIDE vs APLISOL DIAGNOSTIC ANTIGEN