Does APALUTAMIDE Cause Product dose omission in error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product dose omission in error have been filed in association with APALUTAMIDE (ERLEADA). This represents 0.1% of all adverse event reports for APALUTAMIDE.
7
Reports of Product dose omission in error with APALUTAMIDE
0.1%
of all APALUTAMIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission in error From APALUTAMIDE?
Of the 7 reports.
Is Product dose omission in 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 dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which APALUTAMIDE Alternatives Have Lower Product dose omission in error Risk?
APALUTAMIDE vs APATINIB
APALUTAMIDE vs APIDRA
APALUTAMIDE vs APIDRA SOLOSTAR
APALUTAMIDE vs APIXABAN
APALUTAMIDE vs APLISOL DIAGNOSTIC ANTIGEN