Does ABIRATERONE Cause Product administration error? 29 Reports in FDA Database
Prostate Health & Male Vitality — Naturally
ProstaVive: better flow, better sleep, better energy. 180-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Product administration error have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 0.1% of all adverse event reports for ABIRATERONE.
29
Reports of Product administration error with ABIRATERONE
0.1%
of all ABIRATERONE reports
0
Deaths
16
Hospitalizations
How Dangerous Is Product administration error From ABIRATERONE?
Of the 29 reports, 16 (55.2%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABIRATERONE. However, 29 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which ABIRATERONE Alternatives Have Lower Product administration error Risk?
ABIRATERONE vs ABIRATERONE\ABIRATERONE
ABIRATERONE vs ABOBOTULINUMTOXINA
ABIRATERONE vs ABRAXANE
ABIRATERONE vs ABROCITINIB
ABIRATERONE vs ACALABRUTINIB