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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 GOLIMUMAB Cause Device issue? 1,827 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,827 reports of Device issue have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 2.6% of all adverse event reports for GOLIMUMAB.

1,827
Reports of Device issue with GOLIMUMAB
2.6%
of all GOLIMUMAB reports
1
Deaths
9
Hospitalizations

How Dangerous Is Device issue From GOLIMUMAB?

Of the 1,827 reports, 1 (0.1%) resulted in death, 9 (0.5%) required hospitalization.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 1,827 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 issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) USTEKINUMAB (1,716) EVOLOCUMAB (1,659)

Which GOLIMUMAB Alternatives Have Lower Device issue Risk?

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

Related Pages

GOLIMUMAB Full Profile All Device issue Reports All Drugs Causing Device issue GOLIMUMAB Demographics