Does ERYTHROPOIETIN Cause Intercepted product administration error? 301 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 301 reports of Intercepted product administration error have been filed in association with ERYTHROPOIETIN. This represents 3.8% of all adverse event reports for ERYTHROPOIETIN.
301
Reports of Intercepted product administration error with ERYTHROPOIETIN
3.8%
of all ERYTHROPOIETIN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Intercepted product administration error From ERYTHROPOIETIN?
Of the 301 reports, 2 (0.7%) required hospitalization.
Is Intercepted product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERYTHROPOIETIN. However, 301 reports have been filed with the FAERS database.
What Other Side Effects Does ERYTHROPOIETIN Cause?
Product storage error (1,286)
Death (871)
Circumstance or information capable of leading to medication error (592)
Off label use (590)
Haemoglobin decreased (443)
Drug ineffective (370)
Anaemia (367)
Incorrect product storage (268)
Fatigue (266)
Drug dose omission (240)
What Other Drugs Cause Intercepted product administration error?
EVOLOCUMAB (2,508)
DENOSUMAB (1,209)
ERENUMAB-AOOE (1,015)
ETANERCEPT (574)
DARBEPOETIN ALFA (385)
PEGFILGRASTIM (356)
LEUPROLIDE (307)
ROMOSOZUMAB-AQQG (115)
BENZYL ALCOHOL\ETANERCEPT (112)
CARFILZOMIB (102)
Which ERYTHROPOIETIN Alternatives Have Lower Intercepted product administration error Risk?
ERYTHROPOIETIN vs ESCHERICHIA COLI
ERYTHROPOIETIN vs ESCITALOPRAM
ERYTHROPOIETIN vs ESCITALOPRAM OXALATE
ERYTHROPOIETIN vs ESKETAMINE
ERYTHROPOIETIN vs ESLICARBAZEPINE