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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ABIRATERONE Cause Condition aggravated? 161 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 161 reports of Condition aggravated have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 0.5% of all adverse event reports for ABIRATERONE.

161
Reports of Condition aggravated with ABIRATERONE
0.5%
of all ABIRATERONE reports
13
Deaths
67
Hospitalizations

How Dangerous Is Condition aggravated From ABIRATERONE?

Of the 161 reports, 13 (8.1%) resulted in death, 67 (41.6%) required hospitalization, and 8 (5.0%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABIRATERONE. However, 161 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which ABIRATERONE Alternatives Have Lower Condition aggravated Risk?

ABIRATERONE vs ABIRATERONE\ABIRATERONE ABIRATERONE vs ABOBOTULINUMTOXINA ABIRATERONE vs ABRAXANE ABIRATERONE vs ABROCITINIB ABIRATERONE vs ACALABRUTINIB

Related Pages

ABIRATERONE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated ABIRATERONE Demographics