Does ABIRATERONE Cause Hepatic function abnormal? 206 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 206 reports of Hepatic function abnormal have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 0.6% of all adverse event reports for ABIRATERONE.
206
Reports of Hepatic function abnormal with ABIRATERONE
0.6%
of all ABIRATERONE reports
27
Deaths
69
Hospitalizations
How Dangerous Is Hepatic function abnormal From ABIRATERONE?
Of the 206 reports, 27 (13.1%) resulted in death, 69 (33.5%) required hospitalization, and 8 (3.9%) 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 ABIRATERONE. However, 206 reports have been filed with the FAERS database.
What Other Side Effects Does ABIRATERONE Cause?
Death (5,623)
Fatigue (1,928)
Drug ineffective (1,732)
Therapy cessation (1,602)
Prostatic specific antigen increased (1,581)
Disease progression (1,098)
Hospitalisation (1,034)
Hot flush (989)
Asthenia (891)
Off label use (859)
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 ABIRATERONE Alternatives Have Lower Hepatic function abnormal Risk?
ABIRATERONE vs ABIRATERONE\ABIRATERONE
ABIRATERONE vs ABOBOTULINUMTOXINA
ABIRATERONE vs ABRAXANE
ABIRATERONE vs ABROCITINIB
ABIRATERONE vs ACALABRUTINIB