Does GOLIMUMAB Cause Condition aggravated? 5,238 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,238 reports of Condition aggravated have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 7.6% of all adverse event reports for GOLIMUMAB.
5,238
Reports of Condition aggravated with GOLIMUMAB
7.6%
of all GOLIMUMAB reports
1,417
Deaths
2,230
Hospitalizations
How Dangerous Is Condition aggravated From GOLIMUMAB?
Of the 5,238 reports, 1,417 (27.1%) resulted in death, 2,230 (42.6%) required hospitalization, and 1,632 (31.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 5,238 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which GOLIMUMAB Alternatives Have Lower Condition aggravated Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN