Does ERYTHROPOIETIN Cause Product storage error? 1,286 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,286 reports of Product storage error have been filed in association with ERYTHROPOIETIN. This represents 16.2% of all adverse event reports for ERYTHROPOIETIN.
1,286
Reports of Product storage error with ERYTHROPOIETIN
16.2%
of all ERYTHROPOIETIN reports
1
Deaths
20
Hospitalizations
How Dangerous Is Product storage error From ERYTHROPOIETIN?
Of the 1,286 reports, 1 (0.1%) resulted in death, 20 (1.6%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERYTHROPOIETIN. However, 1,286 reports have been filed with the FAERS database.
What Other Side Effects Does ERYTHROPOIETIN Cause?
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)
Drug dose omission (240)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which ERYTHROPOIETIN Alternatives Have Lower Product storage error Risk?
ERYTHROPOIETIN vs ESCHERICHIA COLI
ERYTHROPOIETIN vs ESCITALOPRAM
ERYTHROPOIETIN vs ESCITALOPRAM OXALATE
ERYTHROPOIETIN vs ESKETAMINE
ERYTHROPOIETIN vs ESLICARBAZEPINE