Does ABIRATERONE Cause Device related sepsis? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device related sepsis have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 0.0% of all adverse event reports for ABIRATERONE.
5
Reports of Device related sepsis with ABIRATERONE
0.0%
of all ABIRATERONE reports
1
Deaths
3
Hospitalizations
How Dangerous Is Device related sepsis From ABIRATERONE?
Of the 5 reports, 1 (20.0%) resulted in death, 3 (60.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
Is Device related sepsis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABIRATERONE. However, 5 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 Device related sepsis?
TEDUGLUTIDE (226)
TREPROSTINIL (225)
CYCLOPHOSPHAMIDE (130)
RITUXIMAB (113)
EPOPROSTENOL (89)
CYCLOSPORINE (82)
METHYLPREDNISOLONE (82)
BORTEZOMIB (79)
MACITENTAN (55)
DEXAMETHASONE (53)
Which ABIRATERONE Alternatives Have Lower Device related sepsis Risk?
ABIRATERONE vs ABIRATERONE\ABIRATERONE
ABIRATERONE vs ABOBOTULINUMTOXINA
ABIRATERONE vs ABRAXANE
ABIRATERONE vs ABROCITINIB
ABIRATERONE vs ACALABRUTINIB