Does SECUKINUMAB Cause Duodenal ulcer perforation? 2,253 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,253 reports of Duodenal ulcer perforation have been filed in association with SECUKINUMAB (COSENTYX). This represents 1.5% of all adverse event reports for SECUKINUMAB.
2,253
Reports of Duodenal ulcer perforation with SECUKINUMAB
1.5%
of all SECUKINUMAB reports
1,693
Deaths
1,756
Hospitalizations
How Dangerous Is Duodenal ulcer perforation From SECUKINUMAB?
Of the 2,253 reports, 1,693 (75.1%) resulted in death, 1,756 (77.9%) required hospitalization, and 1,930 (85.7%) 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 SECUKINUMAB. However, 2,253 reports have been filed with the FAERS database.
What Other Side Effects Does SECUKINUMAB Cause?
Drug ineffective (27,434)
Psoriasis (21,976)
Pain (15,244)
Arthralgia (13,769)
Fatigue (9,406)
Psoriatic arthropathy (8,900)
Pruritus (8,755)
Malaise (8,570)
Rash (8,023)
Condition aggravated (7,536)
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 SECUKINUMAB Alternatives Have Lower Duodenal ulcer perforation Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG