Does DARBEPOETIN ALFA Cause Sepsis? 510 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 510 reports of Sepsis have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 1.6% of all adverse event reports for DARBEPOETIN ALFA.
510
Reports of Sepsis with DARBEPOETIN ALFA
1.6%
of all DARBEPOETIN ALFA reports
371
Deaths
336
Hospitalizations
How Dangerous Is Sepsis From DARBEPOETIN ALFA?
Of the 510 reports, 371 (72.7%) resulted in death, 336 (65.9%) required hospitalization, and 118 (23.1%) were considered life-threatening.
Is Sepsis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 510 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 Sepsis?
RITUXIMAB (4,043)
CYCLOPHOSPHAMIDE (4,041)
METHOTREXATE (3,933)
ADALIMUMAB (3,169)
DEXAMETHASONE (3,150)
LENALIDOMIDE (2,956)
VINCRISTINE (2,791)
DOXORUBICIN (2,740)
PREDNISONE (2,634)
PREDNISOLONE (2,281)
Which DARBEPOETIN ALFA Alternatives Have Lower Sepsis Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE