Does ABIRATERONE Cause Product dose omission? 197 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 197 reports of Product dose omission have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 0.6% of all adverse event reports for ABIRATERONE.
197
Reports of Product dose omission with ABIRATERONE
0.6%
of all ABIRATERONE reports
15
Deaths
44
Hospitalizations
How Dangerous Is Product dose omission From ABIRATERONE?
Of the 197 reports, 15 (7.6%) resulted in death, 44 (22.3%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABIRATERONE. However, 197 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ABIRATERONE Alternatives Have Lower Product dose omission Risk?
ABIRATERONE vs ABIRATERONE\ABIRATERONE
ABIRATERONE vs ABOBOTULINUMTOXINA
ABIRATERONE vs ABRAXANE
ABIRATERONE vs ABROCITINIB
ABIRATERONE vs ACALABRUTINIB