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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 Product packaging quantity issue? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product packaging quantity issue have been filed in association with ERYTHROPOIETIN. This represents 0.2% of all adverse event reports for ERYTHROPOIETIN.

12
Reports of Product packaging quantity issue with ERYTHROPOIETIN
0.2%
of all ERYTHROPOIETIN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product packaging quantity issue From ERYTHROPOIETIN?

Of the 12 reports.

Is Product packaging quantity issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ERYTHROPOIETIN. However, 12 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 Product packaging quantity issue?

LEUPROLIDE (523) ALBUTEROL (431) BUDESONIDE\FORMOTEROL (301) FENTANYL (286) BUPRENORPHINE (225) CYCLOSPORINE (206) ESTRADIOL (201) BIMATOPROST (177) RIVAROXABAN (174) EXENATIDE (154)

Which ERYTHROPOIETIN Alternatives Have Lower Product packaging quantity 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 Product packaging quantity issue Reports All Drugs Causing Product packaging quantity issue ERYTHROPOIETIN Demographics