Does ABIRATERONE Cause Adverse event? 360 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 360 reports of Adverse event have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 1.0% of all adverse event reports for ABIRATERONE.
360
Reports of Adverse event with ABIRATERONE
1.0%
of all ABIRATERONE reports
21
Deaths
28
Hospitalizations
How Dangerous Is Adverse event From ABIRATERONE?
Of the 360 reports, 21 (5.8%) resulted in death, 28 (7.8%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for ABIRATERONE.
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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which ABIRATERONE Alternatives Have Lower Adverse event Risk?
ABIRATERONE vs ABIRATERONE\ABIRATERONE
ABIRATERONE vs ABOBOTULINUMTOXINA
ABIRATERONE vs ABRAXANE
ABIRATERONE vs ABROCITINIB
ABIRATERONE vs ACALABRUTINIB