Does DARBEPOETIN ALFA Cause Circumstance or information capable of leading to medication error? 1,050 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,050 reports of Circumstance or information capable of leading to medication error have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 3.2% of all adverse event reports for DARBEPOETIN ALFA.
1,050
Reports of Circumstance or information capable of leading to medication error with DARBEPOETIN ALFA
3.2%
of all DARBEPOETIN ALFA reports
0
Deaths
5
Hospitalizations
How Dangerous Is Circumstance or information capable of leading to medication error From DARBEPOETIN ALFA?
Of the 1,050 reports, 5 (0.5%) required hospitalization.
Is Circumstance or information capable of leading to medication error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 1,050 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)
Haemodialysis (907)
Pneumonia (733)
Fall (726)
Anaemia (562)
Dialysis (555)
Haemoglobin decreased (546)
What Other Drugs Cause Circumstance or information capable of leading to medication error?
EVOLOCUMAB (2,870)
DENOSUMAB (2,078)
ETANERCEPT (1,721)
POLYETHYLENE GLYCOL 3350 (1,278)
ERENUMAB-AOOE (986)
PEGFILGRASTIM (881)
EXENATIDE (732)
BUDESONIDE\FORMOTEROL (640)
APIXABAN (618)
ERYTHROPOIETIN (592)
Which DARBEPOETIN ALFA Alternatives Have Lower Circumstance or information capable of leading to medication error Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE