Does GOLIMUMAB Cause Device use error? 23 Reports in FDA Database

Q: Does GOLIMUMAB cause Device use error?

23 reports of Device use error have been filed with the FDA for GOLIMUMAB, representing 0.0% of all GOLIMUMAB adverse event reports.

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Device use error have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.0% of all adverse event reports for GOLIMUMAB.

Reports of Device use error with GOLIMUMAB

0.0%

of all GOLIMUMAB reports

Deaths

Hospitalizations

How Dangerous Is Device use error From GOLIMUMAB?

Of the 23 reports.

Is Device use error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 23 reports have been filed with the FAERS database.

What Other Side Effects Does GOLIMUMAB Cause?

Drug ineffective (17,959) Rheumatoid arthritis (12,272) Pain (11,443) Fatigue (9,626) Off label use (8,764) Alopecia (8,394) Rash (8,331) Joint swelling (8,264) Arthralgia (7,968) Abdominal discomfort (7,902)

What Other Drugs Cause Device use error?

PEGFILGRASTIM (6,001) ALBUTEROL (5,215) ALBIGLUTIDE (4,056) EVOLOCUMAB (4,002) SOMATROPIN (2,801) FLUTICASONE\SALMETEROL (1,749) FLUTICASONE (783) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766) ERENUMAB-AOOE (711) ETANERCEPT (665)

Which GOLIMUMAB Alternatives Have Lower Device use error Risk?

GOLIMUMAB vs GOLODIRSEN GOLIMUMAB vs GONADORELIN GOLIMUMAB vs GONADOTROPHIN, CHORIONIC GOLIMUMAB vs GOSERELIN GOLIMUMAB vs GRAMICIDIN

GOLIMUMAB Full Profile All Device use error Reports All Drugs Causing Device use error GOLIMUMAB Demographics