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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 Patient-device incompatibility? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Patient-device incompatibility have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.0% of all adverse event reports for GOLIMUMAB.

8
Reports of Patient-device incompatibility with GOLIMUMAB
0.0%
of all GOLIMUMAB reports
1
Deaths
5
Hospitalizations

How Dangerous Is Patient-device incompatibility From GOLIMUMAB?

Of the 8 reports, 1 (12.5%) resulted in death, 5 (62.5%) required hospitalization.

Is Patient-device incompatibility Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 8 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 Patient-device incompatibility?

LEVONORGESTREL (85) ADALIMUMAB (79) SOMATROPIN (44) CARBIDOPA\LEVODOPA (35) SOMATROGON-GHLA (29) ETONOGESTREL (23) TREPROSTINIL (21) BACLOFEN (17) ETANERCEPT (11) ABATACEPT (8)

Which GOLIMUMAB Alternatives Have Lower Patient-device incompatibility Risk?

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

Related Pages

GOLIMUMAB Full Profile All Patient-device incompatibility Reports All Drugs Causing Patient-device incompatibility GOLIMUMAB Demographics