Does ERYTHROPOIETIN Cause Condition aggravated? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Condition aggravated have been filed in association with ERYTHROPOIETIN. This represents 0.5% of all adverse event reports for ERYTHROPOIETIN.
43
Reports of Condition aggravated with ERYTHROPOIETIN
0.5%
of all ERYTHROPOIETIN reports
8
Deaths
10
Hospitalizations
How Dangerous Is Condition aggravated From ERYTHROPOIETIN?
Of the 43 reports, 8 (18.6%) resulted in death, 10 (23.3%) required hospitalization, and 1 (2.3%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERYTHROPOIETIN. However, 43 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ERYTHROPOIETIN Alternatives Have Lower Condition aggravated Risk?
ERYTHROPOIETIN vs ESCHERICHIA COLI
ERYTHROPOIETIN vs ESCITALOPRAM
ERYTHROPOIETIN vs ESCITALOPRAM OXALATE
ERYTHROPOIETIN vs ESKETAMINE
ERYTHROPOIETIN vs ESLICARBAZEPINE