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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 TOCILIZUMAB Cause Hyperkeratosis? 103 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 103 reports of Hyperkeratosis have been filed in association with TOCILIZUMAB (Tocilizumab-anoh). This represents 0.1% of all adverse event reports for TOCILIZUMAB.

103
Reports of Hyperkeratosis with TOCILIZUMAB
0.1%
of all TOCILIZUMAB reports
1
Deaths
20
Hospitalizations

How Dangerous Is Hyperkeratosis From TOCILIZUMAB?

Of the 103 reports, 1 (1.0%) resulted in death, 20 (19.4%) required hospitalization.

Is Hyperkeratosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOCILIZUMAB. However, 103 reports have been filed with the FAERS database.

What Other Side Effects Does TOCILIZUMAB Cause?

Drug ineffective (32,342) Rheumatoid arthritis (20,652) Pain (18,384) Off label use (18,256) Arthralgia (15,536) Joint swelling (14,831) Fatigue (13,802) Rash (12,327) Drug intolerance (11,952) Contraindicated product administered (11,547)

What Other Drugs Cause Hyperkeratosis?

CABOZANTINIB S-MALATE (411) ADALIMUMAB (332) SUNITINIB MALATE (170) ETANERCEPT (168) SORAFENIB (150) METHOTREXATE (149) VEMURAFENIB (145) REGORAFENIB (136) RIPRETINIB (124) RITUXIMAB (121)

Which TOCILIZUMAB Alternatives Have Lower Hyperkeratosis Risk?

TOCILIZUMAB vs TOCILIZUMAB-AAZG TOCILIZUMAB vs TOCOPHEROL TOCILIZUMAB vs TOFACITINIB TOCILIZUMAB vs TOFERSEN TOCILIZUMAB vs TOLNAFTATE

Related Pages

TOCILIZUMAB Full Profile All Hyperkeratosis Reports All Drugs Causing Hyperkeratosis TOCILIZUMAB Demographics