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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 Wrong product administered? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Wrong product administered have been filed in association with ERYTHROPOIETIN. This represents 0.1% of all adverse event reports for ERYTHROPOIETIN.

9
Reports of Wrong product administered with ERYTHROPOIETIN
0.1%
of all ERYTHROPOIETIN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Wrong product administered From ERYTHROPOIETIN?

Of the 9 reports.

Is Wrong product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ERYTHROPOIETIN. However, 9 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 Wrong product administered?

INSULIN LISPRO (337) INSULIN GLARGINE (226) RISPERIDONE (141) QUETIAPINE (137) ACETAMINOPHEN (133) INSULIN ASPART (112) CLOZAPINE (106) INSULIN HUMAN (104) 503 Service Unavailable

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