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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 Performance status decreased? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Performance status decreased have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 0.0% of all adverse event reports for ABIRATERONE.

7
Reports of Performance status decreased with ABIRATERONE
0.0%
of all ABIRATERONE reports
3
Deaths
0
Hospitalizations

How Dangerous Is Performance status decreased From ABIRATERONE?

Of the 7 reports, 3 (42.9%) resulted in death.

Is Performance status decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABIRATERONE. However, 7 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 Performance status decreased?

BACLOFEN (156) LENALIDOMIDE (118) PACLITAXEL (112) BEVACIZUMAB (103) SODIUM OXYBATE (103) CARBOPLATIN (100) DEXAMETHASONE (80) CAPECITABINE (75) NIRAPARIB (75) LUMATEPERONE (68)

Which ABIRATERONE Alternatives Have Lower Performance status decreased Risk?

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

Related Pages

ABIRATERONE Full Profile All Performance status decreased Reports All Drugs Causing Performance status decreased ABIRATERONE Demographics