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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 Product administration error? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product administration error have been filed in association with APALUTAMIDE (ERLEADA). This represents 0.1% of all adverse event reports for APALUTAMIDE.

7
Reports of Product administration error with APALUTAMIDE
0.1%
of all APALUTAMIDE reports
1
Deaths
2
Hospitalizations

How Dangerous Is Product administration error From APALUTAMIDE?

Of the 7 reports, 1 (14.3%) resulted in death, 2 (28.6%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APALUTAMIDE. However, 7 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 Product administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which APALUTAMIDE Alternatives Have Lower Product administration error 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 Product administration error Reports All Drugs Causing Product administration error APALUTAMIDE Demographics