Does ABIRATERONE Cause Wrong technique in product usage process? 179 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 179 reports of Wrong technique in product usage process have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 0.5% of all adverse event reports for ABIRATERONE.
179
Reports of Wrong technique in product usage process with ABIRATERONE
0.5%
of all ABIRATERONE reports
8
Deaths
37
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ABIRATERONE?
Of the 179 reports, 8 (4.5%) resulted in death, 37 (20.7%) required hospitalization, and 1 (0.6%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABIRATERONE. However, 179 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ABIRATERONE Alternatives Have Lower Wrong technique in product usage process Risk?
ABIRATERONE vs ABIRATERONE\ABIRATERONE
ABIRATERONE vs ABOBOTULINUMTOXINA
ABIRATERONE vs ABRAXANE
ABIRATERONE vs ABROCITINIB
ABIRATERONE vs ACALABRUTINIB