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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 ERYTHROPOIETIN Cause Device issue? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Device issue have been filed in association with ERYTHROPOIETIN. This represents 0.1% of all adverse event reports for ERYTHROPOIETIN.

10
Reports of Device issue with ERYTHROPOIETIN
0.1%
of all ERYTHROPOIETIN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device issue From ERYTHROPOIETIN?

Of the 10 reports.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ERYTHROPOIETIN. However, 10 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) Intercepted product administration error (301) Incorrect product storage (268) Fatigue (266)

What Other Drugs Cause Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which ERYTHROPOIETIN Alternatives Have Lower Device issue Risk?

ERYTHROPOIETIN vs ESCHERICHIA COLI ERYTHROPOIETIN vs ESCITALOPRAM ERYTHROPOIETIN vs ESCITALOPRAM OXALATE ERYTHROPOIETIN vs ESKETAMINE ERYTHROPOIETIN vs ESLICARBAZEPINE

Related Pages

ERYTHROPOIETIN Full Profile All Device issue Reports All Drugs Causing Device issue ERYTHROPOIETIN Demographics