Does DARBEPOETIN ALFA Cause Hepatic function abnormal? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Hepatic function abnormal have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 0.1% of all adverse event reports for DARBEPOETIN ALFA.
26
Reports of Hepatic function abnormal with DARBEPOETIN ALFA
0.1%
of all DARBEPOETIN ALFA reports
9
Deaths
16
Hospitalizations
How Dangerous Is Hepatic function abnormal From DARBEPOETIN ALFA?
Of the 26 reports, 9 (34.6%) resulted in death, 16 (61.5%) required hospitalization, and 3 (11.5%) were considered life-threatening.
Is Hepatic function abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 26 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 Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which DARBEPOETIN ALFA Alternatives Have Lower Hepatic function abnormal Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE