Does DARBEPOETIN ALFA Cause Off label use? 1,586 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,586 reports of Off label use have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 4.8% of all adverse event reports for DARBEPOETIN ALFA.
1,586
Reports of Off label use with DARBEPOETIN ALFA
4.8%
of all DARBEPOETIN ALFA reports
364
Deaths
446
Hospitalizations
How Dangerous Is Off label use From DARBEPOETIN ALFA?
Of the 1,586 reports, 364 (23.0%) resulted in death, 446 (28.1%) required hospitalization, and 124 (7.8%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 1,586 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)
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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which DARBEPOETIN ALFA Alternatives Have Lower Off label use Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE