Does DARBEPOETIN ALFA Cause Adverse event? 139 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 139 reports of Adverse event have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 0.4% of all adverse event reports for DARBEPOETIN ALFA.
139
Reports of Adverse event with DARBEPOETIN ALFA
0.4%
of all DARBEPOETIN ALFA reports
27
Deaths
71
Hospitalizations
How Dangerous Is Adverse event From DARBEPOETIN ALFA?
Of the 139 reports, 27 (19.4%) resulted in death, 71 (51.1%) required hospitalization, and 4 (2.9%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 139 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which DARBEPOETIN ALFA Alternatives Have Lower Adverse event Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE