Does ETANERCEPT Cause Incorrect product administration duration? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Incorrect product administration duration have been filed in association with ETANERCEPT (ENBREL). This represents 0.0% of all adverse event reports for ETANERCEPT.
71
Reports of Incorrect product administration duration with ETANERCEPT
0.0%
of all ETANERCEPT reports
56
Deaths
55
Hospitalizations
How Dangerous Is Incorrect product administration duration From ETANERCEPT?
Of the 71 reports, 56 (78.9%) resulted in death, 55 (77.5%) required hospitalization, and 55 (77.5%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETANERCEPT. However, 71 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ETANERCEPT Alternatives Have Lower Incorrect product administration duration Risk?
ETANERCEPT vs ETANERCEPT-SZZS
ETANERCEPT vs ETELCALCETIDE
ETANERCEPT vs ETEPLIRSEN
ETANERCEPT vs ETESEVIMAB
ETANERCEPT vs ETHACRYNIC ACID