Does DARBEPOETIN ALFA Cause Drug hypersensitivity? 154 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 154 reports of Drug hypersensitivity have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 0.5% of all adverse event reports for DARBEPOETIN ALFA.
154
Reports of Drug hypersensitivity with DARBEPOETIN ALFA
0.5%
of all DARBEPOETIN ALFA reports
109
Deaths
123
Hospitalizations
How Dangerous Is Drug hypersensitivity From DARBEPOETIN ALFA?
Of the 154 reports, 109 (70.8%) resulted in death, 123 (79.9%) required hospitalization, and 103 (66.9%) were considered life-threatening.
Is Drug hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 154 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 Drug hypersensitivity?
METHOTREXATE (16,677)
ETANERCEPT (12,991)
ADALIMUMAB (11,599)
MORPHINE (11,095)
RITUXIMAB (8,924)
LEFLUNOMIDE (8,148)
INFLIXIMAB (8,119)
TOCILIZUMAB (7,883)
ABATACEPT (7,808)
CODEINE (7,479)
Which DARBEPOETIN ALFA Alternatives Have Lower Drug hypersensitivity Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE