Does DARBEPOETIN ALFA Cause Condition aggravated? 234 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 234 reports of Condition aggravated have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 0.7% of all adverse event reports for DARBEPOETIN ALFA.
234
Reports of Condition aggravated with DARBEPOETIN ALFA
0.7%
of all DARBEPOETIN ALFA reports
160
Deaths
180
Hospitalizations
How Dangerous Is Condition aggravated From DARBEPOETIN ALFA?
Of the 234 reports, 160 (68.4%) resulted in death, 180 (76.9%) required hospitalization, and 105 (44.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 234 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DARBEPOETIN ALFA Alternatives Have Lower Condition aggravated Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE