Does ERYTHROPOIETIN Cause Hypersensitivity? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Hypersensitivity have been filed in association with ERYTHROPOIETIN. This represents 0.9% of all adverse event reports for ERYTHROPOIETIN.
71
Reports of Hypersensitivity with ERYTHROPOIETIN
0.9%
of all ERYTHROPOIETIN reports
0
Deaths
17
Hospitalizations
How Dangerous Is Hypersensitivity From ERYTHROPOIETIN?
Of the 71 reports, 17 (23.9%) required hospitalization, and 1 (1.4%) were considered life-threatening.
Is Hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERYTHROPOIETIN. However, 71 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 Hypersensitivity?
ETANERCEPT (10,846)
ADALIMUMAB (10,641)
METHOTREXATE (9,799)
TOCILIZUMAB (9,076)
ABATACEPT (8,945)
INFLIXIMAB (8,519)
RITUXIMAB (8,408)
ADAPALENE (8,356)
LEFLUNOMIDE (7,926)
CERTOLIZUMAB PEGOL (7,353)
Which ERYTHROPOIETIN Alternatives Have Lower Hypersensitivity Risk?
ERYTHROPOIETIN vs ESCHERICHIA COLI
ERYTHROPOIETIN vs ESCITALOPRAM
ERYTHROPOIETIN vs ESCITALOPRAM OXALATE
ERYTHROPOIETIN vs ESKETAMINE
ERYTHROPOIETIN vs ESLICARBAZEPINE