Does DARBEPOETIN ALFA Cause Device occlusion? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Device occlusion have been filed in association with DARBEPOETIN ALFA (ARANESP). This represents 0.0% of all adverse event reports for DARBEPOETIN ALFA.
14
Reports of Device occlusion with DARBEPOETIN ALFA
0.0%
of all DARBEPOETIN ALFA reports
2
Deaths
12
Hospitalizations
How Dangerous Is Device occlusion From DARBEPOETIN ALFA?
Of the 14 reports, 2 (14.3%) resulted in death, 12 (85.7%) required hospitalization, and 1 (7.1%) were considered life-threatening.
Is Device occlusion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARBEPOETIN ALFA. However, 14 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 Device occlusion?
PEGFILGRASTIM (3,239)
CARBIDOPA\LEVODOPA (1,464)
SOMATROPIN (823)
LEUPROLIDE (786)
EPOPROSTENOL (580)
TREPROSTINIL (458)
ALBUTEROL (431)
MEDROXYPROGESTERONE (284)
BACLOFEN (254)
LEVODOPA (224)
Which DARBEPOETIN ALFA Alternatives Have Lower Device occlusion Risk?
DARBEPOETIN ALFA vs DARIDOREXANT
DARBEPOETIN ALFA vs DARIFENACIN HYDROBROMIDE
DARBEPOETIN ALFA vs DAROLUTAMIDE
DARBEPOETIN ALFA vs DARUNAVIR
DARBEPOETIN ALFA vs DARUNAVIR ETHANOLATE