Does DARBEPOETIN ALFA Cause Intercepted product administration error? 385 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 385 reports of Intercepted product administration error have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 1.2% of all adverse event reports for DARBEPOETIN ALFA.
385
Reports of Intercepted product administration error with DARBEPOETIN ALFA
1.2%
of all DARBEPOETIN ALFA reports
0
Deaths
3
Hospitalizations
How Dangerous Is Intercepted product administration error From DARBEPOETIN ALFA?
Of the 385 reports, 3 (0.8%) required hospitalization.
Is Intercepted product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 385 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 Intercepted product administration error?
EVOLOCUMAB (2,508)
DENOSUMAB (1,209)
ERENUMAB-AOOE (1,015)
ETANERCEPT (574)
PEGFILGRASTIM (356)
LEUPROLIDE (307)
ERYTHROPOIETIN (301)
ROMOSOZUMAB-AQQG (115)
BENZYL ALCOHOL\ETANERCEPT (112)
CARFILZOMIB (102)
Which DARBEPOETIN ALFA Alternatives Have Lower Intercepted product administration error Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE