Does SIRUKUMAB Cause Duodenal ulcer perforation? 364 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 364 reports of Duodenal ulcer perforation have been filed in association with SIRUKUMAB. This represents 27.1% of all adverse event reports for SIRUKUMAB.
364
Reports of Duodenal ulcer perforation with SIRUKUMAB
27.1%
of all SIRUKUMAB reports
325
Deaths
312
Hospitalizations
How Dangerous Is Duodenal ulcer perforation From SIRUKUMAB?
Of the 364 reports, 325 (89.3%) resulted in death, 312 (85.7%) required hospitalization, and 282 (77.5%) 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 SIRUKUMAB. However, 364 reports have been filed with the FAERS database.
What Other Side Effects Does SIRUKUMAB Cause?
Off label use (798)
Drug ineffective (775)
Rheumatoid arthritis (663)
Nausea (656)
Pain (629)
Synovitis (623)
General physical health deterioration (619)
Rash (565)
Pericarditis (562)
Pemphigus (561)
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 SIRUKUMAB Alternatives Have Lower Duodenal ulcer perforation Risk?
SIRUKUMAB vs SITAGLIPTIN
SIRUKUMAB vs SOAP
SIRUKUMAB vs SODIUM
SIRUKUMAB vs SODIUM BICARBONATE
SIRUKUMAB vs SODIUM BICARBONATE\SODIUM