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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 NIVOLUMAB Cause Hyperkeratosis? 76 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Hyperkeratosis have been filed in association with NIVOLUMAB (OPDIVO). This represents 0.1% of all adverse event reports for NIVOLUMAB.

76
Reports of Hyperkeratosis with NIVOLUMAB
0.1%
of all NIVOLUMAB reports
2
Deaths
13
Hospitalizations

How Dangerous Is Hyperkeratosis From NIVOLUMAB?

Of the 76 reports, 2 (2.6%) resulted in death, 13 (17.1%) required hospitalization.

Is Hyperkeratosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NIVOLUMAB. However, 76 reports have been filed with the FAERS database.

What Other Side Effects Does NIVOLUMAB Cause?

Death (11,216) Malignant neoplasm progression (9,363) Off label use (5,208) Diarrhoea (4,692) Fatigue (3,709) Pyrexia (3,454) Intentional product use issue (3,297) Rash (2,816) Nausea (2,805) Decreased appetite (2,619)

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 NIVOLUMAB Alternatives Have Lower Hyperkeratosis Risk?

NIVOLUMAB vs NIVOLUMAB\RELATLIMAB-RMBW NIVOLUMAB vs NIZATIDINE NIVOLUMAB vs NOMEGESTROL NIVOLUMAB vs NORDAZEPAM NIVOLUMAB vs NOREPINEPHRINE

Related Pages

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