Does DARBEPOETIN ALFA Cause Unevaluable event? 414 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 414 reports of Unevaluable event have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 1.3% of all adverse event reports for DARBEPOETIN ALFA.
414
Reports of Unevaluable event with DARBEPOETIN ALFA
1.3%
of all DARBEPOETIN ALFA reports
70
Deaths
283
Hospitalizations
How Dangerous Is Unevaluable event From DARBEPOETIN ALFA?
Of the 414 reports, 70 (16.9%) resulted in death, 283 (68.4%) required hospitalization, and 4 (1.0%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 414 reports have been filed with the FAERS database.
What Other Side Effects Does DARBEPOETIN ALFA Cause?
Death (12,264)
Hospitalisation (5,682)
Product storage error (1,619)
Off label use (1,586)
Circumstance or information capable of leading to medication error (1,050)
Haemodialysis (907)
Pneumonia (733)
Fall (726)
Anaemia (562)
Dialysis (555)
What Other Drugs Cause Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which DARBEPOETIN ALFA Alternatives Have Lower Unevaluable event Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE