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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 APALUTAMIDE Cause Haemoglobin decreased? 40 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Haemoglobin decreased have been filed in association with APALUTAMIDE (ERLEADA). This represents 0.4% of all adverse event reports for APALUTAMIDE.

40
Reports of Haemoglobin decreased with APALUTAMIDE
0.4%
of all APALUTAMIDE reports
2
Deaths
18
Hospitalizations

How Dangerous Is Haemoglobin decreased From APALUTAMIDE?

Of the 40 reports, 2 (5.0%) resulted in death, 18 (45.0%) required hospitalization.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APALUTAMIDE. However, 40 reports have been filed with the FAERS database.

What Other Side Effects Does APALUTAMIDE Cause?

Rash (1,117) Death (1,008) Fatigue (824) Hot flush (532) Product dose omission issue (384) Diarrhoea (317) Asthenia (303) Dizziness (294) Fall (268) Off label use (257)

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 APALUTAMIDE Alternatives Have Lower Haemoglobin decreased Risk?

APALUTAMIDE vs APATINIB APALUTAMIDE vs APIDRA APALUTAMIDE vs APIDRA SOLOSTAR APALUTAMIDE vs APIXABAN APALUTAMIDE vs APLISOL DIAGNOSTIC ANTIGEN

Related Pages

APALUTAMIDE Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased APALUTAMIDE Demographics