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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ETANERCEPT-SZZS Cause Device defective? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device defective have been filed in association with ETANERCEPT-SZZS. This represents 0.1% of all adverse event reports for ETANERCEPT-SZZS.

8
Reports of Device defective with ETANERCEPT-SZZS
0.1%
of all ETANERCEPT-SZZS reports
0
Deaths
2
Hospitalizations

How Dangerous Is Device defective From ETANERCEPT-SZZS?

Of the 8 reports, 2 (25.0%) required hospitalization.

Is Device defective Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ETANERCEPT-SZZS. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does ETANERCEPT-SZZS Cause?

Drug ineffective (4,809) Rheumatoid arthritis (4,586) Pain (4,526) Fatigue (4,044) Arthralgia (3,758) Off label use (3,663) Alopecia (3,620) Rash (3,564) Abdominal discomfort (3,520) Joint swelling (3,512)

What Other Drugs Cause Device defective?

SOMATROPIN (1,719) USTEKINUMAB (1,071) SECUKINUMAB (666) GUSELKUMAB (574) GOLIMUMAB (539) ABATACEPT (458) ALBUTEROL (445) TOCILIZUMAB (400) INSULIN GLARGINE (397) EXENATIDE (387)

Which ETANERCEPT-SZZS Alternatives Have Lower Device defective Risk?

ETANERCEPT-SZZS vs ETELCALCETIDE ETANERCEPT-SZZS vs ETEPLIRSEN ETANERCEPT-SZZS vs ETESEVIMAB ETANERCEPT-SZZS vs ETHACRYNIC ACID ETANERCEPT-SZZS vs ETHAMBUTOL

Related Pages

ETANERCEPT-SZZS Full Profile All Device defective Reports All Drugs Causing Device defective ETANERCEPT-SZZS Demographics