Does ERYTHROPOIETIN Cause Incorrect product storage? 268 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 268 reports of Incorrect product storage have been filed in association with ERYTHROPOIETIN. This represents 3.4% of all adverse event reports for ERYTHROPOIETIN.
268
Reports of Incorrect product storage with ERYTHROPOIETIN
3.4%
of all ERYTHROPOIETIN reports
0
Deaths
9
Hospitalizations
How Dangerous Is Incorrect product storage From ERYTHROPOIETIN?
Of the 268 reports, 9 (3.4%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERYTHROPOIETIN. However, 268 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)
Fatigue (266)
Drug dose omission (240)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
CYCLOSPORINE (203)
Which ERYTHROPOIETIN Alternatives Have Lower Incorrect product storage Risk?
ERYTHROPOIETIN vs ESCHERICHIA COLI
ERYTHROPOIETIN vs ESCITALOPRAM
ERYTHROPOIETIN vs ESCITALOPRAM OXALATE
ERYTHROPOIETIN vs ESKETAMINE
ERYTHROPOIETIN vs ESLICARBAZEPINE