Does DARBEPOETIN ALFA Cause Wrong technique in product usage process? 149 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 149 reports of Wrong technique in product usage process have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 0.5% of all adverse event reports for DARBEPOETIN ALFA.
149
Reports of Wrong technique in product usage process with DARBEPOETIN ALFA
0.5%
of all DARBEPOETIN ALFA reports
2
Deaths
5
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DARBEPOETIN ALFA?
Of the 149 reports, 2 (1.3%) resulted in death, 5 (3.4%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 149 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DARBEPOETIN ALFA Alternatives Have Lower Wrong technique in product usage process Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE