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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 Adverse event? 1,333 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,333 reports of Adverse event have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 1.9% of all adverse event reports for GOLIMUMAB.

1,333
Reports of Adverse event with GOLIMUMAB
1.9%
of all GOLIMUMAB reports
426
Deaths
571
Hospitalizations

How Dangerous Is Adverse event From GOLIMUMAB?

Of the 1,333 reports, 426 (32.0%) resulted in death, 571 (42.8%) required hospitalization, and 511 (38.3%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for GOLIMUMAB.

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 Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which GOLIMUMAB Alternatives Have Lower Adverse event Risk?

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

Related Pages

GOLIMUMAB Full Profile All Adverse event Reports All Drugs Causing Adverse event GOLIMUMAB Demographics