Does GOLIMUMAB Cause Duodenal ulcer perforation? 3,770 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,770 reports of Duodenal ulcer perforation have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 5.5% of all adverse event reports for GOLIMUMAB.
3,770
Reports of Duodenal ulcer perforation with GOLIMUMAB
5.5%
of all GOLIMUMAB reports
1,580
Deaths
1,922
Hospitalizations
How Dangerous Is Duodenal ulcer perforation From GOLIMUMAB?
Of the 3,770 reports, 1,580 (41.9%) resulted in death, 1,922 (51.0%) required hospitalization, and 1,833 (48.6%) were considered life-threatening.
Is Duodenal ulcer perforation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 3,770 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 Duodenal ulcer perforation?
METHOTREXATE (4,239)
LEFLUNOMIDE (4,200)
FOLIC ACID (4,152)
ABATACEPT (4,147)
TOCILIZUMAB (4,130)
DICLOFENAC (4,120)
CETIRIZINE (4,117)
DESOXIMETASONE (4,084)
RITUXIMAB (4,081)
PREDNISONE (4,060)
Which GOLIMUMAB Alternatives Have Lower Duodenal ulcer perforation Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN