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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 Ocular hyperaemia? 68 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Ocular hyperaemia have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.1% of all adverse event reports for GOLIMUMAB.

68
Reports of Ocular hyperaemia with GOLIMUMAB
0.1%
of all GOLIMUMAB reports
16
Deaths
27
Hospitalizations

How Dangerous Is Ocular hyperaemia From GOLIMUMAB?

Of the 68 reports, 16 (23.5%) resulted in death, 27 (39.7%) required hospitalization, and 17 (25.0%) were considered life-threatening.

Is Ocular hyperaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 68 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 Ocular hyperaemia?

DUPILUMAB (6,938) CYCLOSPORINE (1,508) BIMATOPROST (1,447) CENEGERMIN-BKBJ (1,226) BRIMONIDINE (917) ADALIMUMAB (714) LATANOPROST (587) DORZOLAMIDE\TIMOLOL (581) LIFITEGRAST (570) TRAVOPROST (478)

Which GOLIMUMAB Alternatives Have Lower Ocular hyperaemia Risk?

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

Related Pages

GOLIMUMAB Full Profile All Ocular hyperaemia Reports All Drugs Causing Ocular hyperaemia GOLIMUMAB Demographics