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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 Onychomadesis? 420 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 420 reports of Onychomadesis have been filed in association with SIRUKUMAB. This represents 31.2% of all adverse event reports for SIRUKUMAB.

420
Reports of Onychomadesis with SIRUKUMAB
31.2%
of all SIRUKUMAB reports
372
Deaths
377
Hospitalizations

How Dangerous Is Onychomadesis From SIRUKUMAB?

Of the 420 reports, 372 (88.6%) resulted in death, 377 (89.8%) required hospitalization, and 329 (78.3%) were considered life-threatening.

Is Onychomadesis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SIRUKUMAB. However, 420 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 Onychomadesis?

ADALIMUMAB (797) METHOTREXATE (785) RITUXIMAB (722) TOCILIZUMAB (721) ABATACEPT (703) INFLIXIMAB (682) SECUKINUMAB (678) LEFLUNOMIDE (667) GOLIMUMAB (660) HYDROXYCHLOROQUINE (660)

Which SIRUKUMAB Alternatives Have Lower Onychomadesis 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 Onychomadesis Reports All Drugs Causing Onychomadesis SIRUKUMAB Demographics