Does BICALUTAMIDE Cause Haemoglobin decreased? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Haemoglobin decreased have been filed in association with BICALUTAMIDE (Bicalutamide). This represents 1.3% of all adverse event reports for BICALUTAMIDE.
52
Reports of Haemoglobin decreased with BICALUTAMIDE
1.3%
of all BICALUTAMIDE reports
4
Deaths
37
Hospitalizations
How Dangerous Is Haemoglobin decreased From BICALUTAMIDE?
Of the 52 reports, 4 (7.7%) resulted in death, 37 (71.2%) required hospitalization, and 2 (3.8%) 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 BICALUTAMIDE. However, 52 reports have been filed with the FAERS database.
What Other Side Effects Does BICALUTAMIDE Cause?
Malignant neoplasm progression (352)
Prostatic specific antigen increased (322)
Drug ineffective (268)
Fatigue (258)
Prostate cancer (258)
Asthenia (223)
Hot flush (219)
Off label use (171)
Disease progression (169)
Anaemia (164)
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 BICALUTAMIDE Alternatives Have Lower Haemoglobin decreased Risk?
BICALUTAMIDE vs BICTEGRAVIR
BICALUTAMIDE vs BICTEGRAVIR\EMTRICITABINE\TENOFOVIR ALAFENAMIDE
BICALUTAMIDE vs BIFIDOBACTERIUM LONGUM
BICALUTAMIDE vs BIFIDOBACTERIUM LONGUM SUBSP. INFANTIS
BICALUTAMIDE vs BILASTINE