Does ETANERCEPT Cause Product dose omission issue? 1,873 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,873 reports of Product dose omission issue have been filed in association with ETANERCEPT (ENBREL). This represents 0.5% of all adverse event reports for ETANERCEPT.
1,873
Reports of Product dose omission issue with ETANERCEPT
0.5%
of all ETANERCEPT reports
34
Deaths
253
Hospitalizations
How Dangerous Is Product dose omission issue From ETANERCEPT?
Of the 1,873 reports, 34 (1.8%) resulted in death, 253 (13.5%) required hospitalization, and 36 (1.9%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETANERCEPT. However, 1,873 reports have been filed with the FAERS database.
What Other Side Effects Does ETANERCEPT Cause?
Drug ineffective (60,367)
Rheumatoid arthritis (33,166)
Pain (31,961)
Arthralgia (27,429)
Injection site pain (24,717)
Off label use (20,178)
Fatigue (19,907)
Joint swelling (18,462)
Injection site erythema (17,736)
Condition aggravated (15,897)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which ETANERCEPT Alternatives Have Lower Product dose omission issue Risk?
ETANERCEPT vs ETANERCEPT-SZZS
ETANERCEPT vs ETELCALCETIDE
ETANERCEPT vs ETEPLIRSEN
ETANERCEPT vs ETESEVIMAB
ETANERCEPT vs ETHACRYNIC ACID