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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SIRUKUMAB Cause Condition aggravated? 493 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 493 reports of Condition aggravated have been filed in association with SIRUKUMAB. This represents 36.7% of all adverse event reports for SIRUKUMAB.

493
Reports of Condition aggravated with SIRUKUMAB
36.7%
of all SIRUKUMAB reports
366
Deaths
344
Hospitalizations

How Dangerous Is Condition aggravated From SIRUKUMAB?

Of the 493 reports, 366 (74.2%) resulted in death, 344 (69.8%) required hospitalization, and 302 (61.3%) 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 SIRUKUMAB. However, 493 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 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 SIRUKUMAB Alternatives Have Lower Condition aggravated Risk?

SIRUKUMAB vs SITAGLIPTIN SIRUKUMAB vs SOAP SIRUKUMAB vs SODIUM SIRUKUMAB vs SODIUM BICARBONATE SIRUKUMAB vs SODIUM BICARBONATE\SODIUM

Related Pages

SIRUKUMAB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated SIRUKUMAB Demographics