Does SIRUKUMAB Cause Intentional product use issue? 425 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 425 reports of Intentional product use issue have been filed in association with SIRUKUMAB. This represents 31.6% of all adverse event reports for SIRUKUMAB.
425
Reports of Intentional product use issue with SIRUKUMAB
31.6%
of all SIRUKUMAB reports
378
Deaths
339
Hospitalizations
How Dangerous Is Intentional product use issue From SIRUKUMAB?
Of the 425 reports, 378 (88.9%) resulted in death, 339 (79.8%) required hospitalization, and 324 (76.2%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIRUKUMAB. However, 425 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which SIRUKUMAB Alternatives Have Lower Intentional product use issue Risk?
SIRUKUMAB vs SITAGLIPTIN
SIRUKUMAB vs SOAP
SIRUKUMAB vs SODIUM
SIRUKUMAB vs SODIUM BICARBONATE
SIRUKUMAB vs SODIUM BICARBONATE\SODIUM