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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 Eosinophil count increased? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Eosinophil count increased have been filed in association with APALUTAMIDE (ERLEADA). This represents 0.1% of all adverse event reports for APALUTAMIDE.

8
Reports of Eosinophil count increased with APALUTAMIDE
0.1%
of all APALUTAMIDE reports
2
Deaths
5
Hospitalizations

How Dangerous Is Eosinophil count increased From APALUTAMIDE?

Of the 8 reports, 2 (25.0%) resulted in death, 5 (62.5%) required hospitalization, and 1 (12.5%) were considered life-threatening.

Is Eosinophil count increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APALUTAMIDE. However, 8 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 Eosinophil count increased?

ALBUTEROL (1,359) PREDNISONE (846) BUDESONIDE\FORMOTEROL (719) DUPILUMAB (712) TIOTROPIUM (682) MEPOLIZUMAB (670) MONTELUKAST (504) BUDESONIDE (493) CLOZAPINE (475) FLUTICASONE\SALMETEROL (416)

Which APALUTAMIDE Alternatives Have Lower Eosinophil count increased 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 Eosinophil count increased Reports All Drugs Causing Eosinophil count increased APALUTAMIDE Demographics