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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 Contraindicated product administered? 526 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 526 reports of Contraindicated product administered have been filed in association with SIRUKUMAB. This represents 39.1% of all adverse event reports for SIRUKUMAB.

526
Reports of Contraindicated product administered with SIRUKUMAB
39.1%
of all SIRUKUMAB reports
374
Deaths
367
Hospitalizations

How Dangerous Is Contraindicated product administered From SIRUKUMAB?

Of the 526 reports, 374 (71.1%) resulted in death, 367 (69.8%) required hospitalization, and 326 (62.0%) were considered life-threatening.

Is Contraindicated product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SIRUKUMAB. However, 526 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 Contraindicated product administered?

ABATACEPT (13,559) METHOTREXATE (13,121) ETANERCEPT (12,062) TOCILIZUMAB (11,547) ADALIMUMAB (11,270) LEFLUNOMIDE (11,206) HYDROXYCHLOROQUINE (10,557) RITUXIMAB (10,479) INFLIXIMAB (9,618) SULFASALAZINE (8,698)

Which SIRUKUMAB Alternatives Have Lower Contraindicated product administered 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 Contraindicated product administered Reports All Drugs Causing Contraindicated product administered SIRUKUMAB Demographics