Does GOLIMUMAB Cause Product label issue? 76 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Product label issue have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.1% of all adverse event reports for GOLIMUMAB.
76
Reports of Product label issue with GOLIMUMAB
0.1%
of all GOLIMUMAB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product label issue From GOLIMUMAB?
Of the 76 reports, 1 (1.3%) required hospitalization.
Is Product label issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 76 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 label issue?
RIVAROXABAN (379)
ACETAMINOPHEN (276)
GUSELKUMAB (177)
USTEKINUMAB (164)
DIMETHICONE\LOPERAMIDE (154)
CETIRIZINE (138)
IBUPROFEN (99)
POLYETHYLENE GLYCOL 3350 (76)
FENTANYL (72)
LOPERAMIDE (72)
Which GOLIMUMAB Alternatives Have Lower Product label issue Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN