Does GOLIMUMAB Cause Product use issue? 5,669 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,669 reports of Product use issue have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 8.2% of all adverse event reports for GOLIMUMAB.
5,669
Reports of Product use issue with GOLIMUMAB
8.2%
of all GOLIMUMAB reports
839
Deaths
1,742
Hospitalizations
How Dangerous Is Product use issue From GOLIMUMAB?
Of the 5,669 reports, 839 (14.8%) resulted in death, 1,742 (30.7%) required hospitalization, and 1,142 (20.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 5,669 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which GOLIMUMAB Alternatives Have Lower Product use issue Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN