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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

DARBEPOETIN ALFA for Off label use: Side Effects & Safety Data

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There are 29 adverse event reports in the FDA FAERS database where DARBEPOETIN ALFA was used for Off label use.

Most Reported Side Effects for DARBEPOETIN ALFA

Side Effect Reports % Deaths Hosp.
Death 12,264 37.4% 12,260 2,158
Hospitalisation 5,682 17.3% 1,161 5,657
Product storage error 1,619 4.9% 3 28
Off label use 1,586 4.8% 364 446
Circumstance or information capable of leading to medication error 1,050 3.2% 0 5
Haemodialysis 907 2.8% 53 464
Pneumonia 733 2.2% 235 630
Fall 726 2.2% 125 648
Anaemia 562 1.7% 162 390
Dialysis 555 1.7% 37 191
Haemoglobin decreased 546 1.7% 47 284
Malaise 529 1.6% 113 397
Sepsis 510 1.6% 371 336
Dyspnoea 425 1.3% 144 328
Renal disorder 416 1.3% 67 340

Other Indications for DARBEPOETIN ALFA

Product used for unknown indication (21,427) Nephrogenic anaemia (5,332) Anaemia (2,096) Chronic kidney disease (1,293) Myelodysplastic syndrome (1,164) Anaemia of malignant disease (155) Renal disorder (152) Renal failure (128) End stage renal disease (64) Renal transplant (53)

Other Drugs Used for Off label use

LENALIDOMIDE (5,767) ECULIZUMAB (3,550) CERTOLIZUMAB PEGOL (2,256) ABOBOTULINUMTOXINA (2,170) LEVETIRACETAM (2,161) APREMILAST (1,995) PROPRANOLOL (1,576) CETIRIZINE (1,416) HUMAN IMMUNOGLOBULIN G (1,129) THALIDOMIDE (1,033)

Related Pages

DARBEPOETIN ALFA Full Profile All Off label use Drugs DARBEPOETIN ALFA Demographics DARBEPOETIN ALFA Timeline