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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 Condition aggravated? 26 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Condition aggravated have been filed in association with APALUTAMIDE (ERLEADA). This represents 0.3% of all adverse event reports for APALUTAMIDE.

26
Reports of Condition aggravated with APALUTAMIDE
0.3%
of all APALUTAMIDE reports
3
Deaths
8
Hospitalizations

How Dangerous Is Condition aggravated From APALUTAMIDE?

Of the 26 reports, 3 (11.5%) resulted in death, 8 (30.8%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APALUTAMIDE. However, 26 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which APALUTAMIDE Alternatives Have Lower Condition aggravated 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 Condition aggravated Reports All Drugs Causing Condition aggravated APALUTAMIDE Demographics