Does DARBEPOETIN ALFA Cause Product storage error? 1,619 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,619 reports of Product storage error have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 4.9% of all adverse event reports for DARBEPOETIN ALFA.
1,619
Reports of Product storage error with DARBEPOETIN ALFA
4.9%
of all DARBEPOETIN ALFA reports
3
Deaths
28
Hospitalizations
How Dangerous Is Product storage error From DARBEPOETIN ALFA?
Of the 1,619 reports, 3 (0.2%) resulted in death, 28 (1.7%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 1,619 reports have been filed with the FAERS database.
What Other Side Effects Does DARBEPOETIN ALFA Cause?
Death (12,264)
Hospitalisation (5,682)
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)
Haemoglobin decreased (546)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
INSULIN LISPRO (1,448)
USTEKINUMAB (1,338)
Which DARBEPOETIN ALFA Alternatives Have Lower Product storage error Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE