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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 Investigation? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Investigation have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 0.0% of all adverse event reports for ABIRATERONE.

5
Reports of Investigation with ABIRATERONE
0.0%
of all ABIRATERONE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Investigation From ABIRATERONE?

Of the 5 reports, 4 (80.0%) required hospitalization.

Is Investigation Listed in the Official Label?

Yes, Investigation is listed as a known adverse reaction in the official FDA drug label for ABIRATERONE.

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 Investigation?

ARANESP (403) NEULASTA (371) XGEVA (115) FLUTICASONE\SALMETEROL (96) DARBEPOETIN ALFA (86) ADVAIR (77) DENOSUMAB (65) ADVAIR HFA (51) ALBUTEROL (51) VENTOLIN (47)

Which ABIRATERONE Alternatives Have Lower Investigation Risk?

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

Related Pages

ABIRATERONE Full Profile All Investigation Reports All Drugs Causing Investigation ABIRATERONE Demographics