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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DARBEPOETIN ALFA Cause Complication associated with device? 17 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Complication associated with device have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 0.1% of all adverse event reports for DARBEPOETIN ALFA.

17
Reports of Complication associated with device with DARBEPOETIN ALFA
0.1%
of all DARBEPOETIN ALFA reports
3
Deaths
15
Hospitalizations

How Dangerous Is Complication associated with device From DARBEPOETIN ALFA?

Of the 17 reports, 3 (17.6%) resulted in death, 15 (88.2%) required hospitalization.

Is Complication associated with device Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 17 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 Complication associated with device?

ETONOGESTREL (6,047) COPPER (1,083) BACLOFEN (525) TREPROSTINIL (422) EPOPROSTENOL (399) LEVONORGESTREL (344) ADALIMUMAB (269) CARBIDOPA\LEVODOPA (169) MACITENTAN (169) TEDUGLUTIDE (133)

Which DARBEPOETIN ALFA Alternatives Have Lower Complication associated with device Risk?

DARBEPOETIN ALFA vs DARIDOREXANT DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE DARBEPOETIN ALFA vs DAROLUTAMIDE DARBEPOETIN ALFA vs DARUNAVIR DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE

Related Pages

DARBEPOETIN ALFA Full Profile All Complication associated with device Reports All Drugs Causing Complication associated with device DARBEPOETIN ALFA Demographics