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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 Hepatic function abnormal? 34 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Hepatic function abnormal have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.1% of all adverse event reports for GOLIMUMAB.

34
Reports of Hepatic function abnormal with GOLIMUMAB
0.1%
of all GOLIMUMAB reports
2
Deaths
14
Hospitalizations

How Dangerous Is Hepatic function abnormal From GOLIMUMAB?

Of the 34 reports, 2 (5.9%) resulted in death, 14 (41.2%) required hospitalization, and 1 (2.9%) were considered life-threatening.

Is Hepatic function abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 34 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 Hepatic function abnormal?

NIVOLUMAB (1,131) PEMBROLIZUMAB (1,079) METHOTREXATE (1,054) CABOZANTINIB S-MALATE (912) CYCLOPHOSPHAMIDE (824) BEVACIZUMAB (769) PACLITAXEL (603) LENVATINIB (528) ATORVASTATIN (520) CYCLOSPORINE (508)

Which GOLIMUMAB Alternatives Have Lower Hepatic function abnormal Risk?

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

Related Pages

GOLIMUMAB Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal GOLIMUMAB Demographics