Does ABIRATERONE Cause Haemoglobin decreased? 140 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 140 reports of Haemoglobin decreased have been filed in association with ABIRATERONE (Abiraterone Acetate). This represents 0.4% of all adverse event reports for ABIRATERONE.
140
Reports of Haemoglobin decreased with ABIRATERONE
0.4%
of all ABIRATERONE reports
15
Deaths
96
Hospitalizations
How Dangerous Is Haemoglobin decreased From ABIRATERONE?
Of the 140 reports, 15 (10.7%) resulted in death, 96 (68.6%) required hospitalization, and 5 (3.6%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABIRATERONE. However, 140 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which ABIRATERONE Alternatives Have Lower Haemoglobin decreased Risk?
ABIRATERONE vs ABIRATERONE\ABIRATERONE
ABIRATERONE vs ABOBOTULINUMTOXINA
ABIRATERONE vs ABRAXANE
ABIRATERONE vs ABROCITINIB
ABIRATERONE vs ACALABRUTINIB