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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 Condition aggravated? 567 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 567 reports of Condition aggravated have been filed in association with NIVOLUMAB (OPDIVO). This represents 0.7% of all adverse event reports for NIVOLUMAB.

567
Reports of Condition aggravated with NIVOLUMAB
0.7%
of all NIVOLUMAB reports
120
Deaths
289
Hospitalizations

How Dangerous Is Condition aggravated From NIVOLUMAB?

Of the 567 reports, 120 (21.2%) resulted in death, 289 (51.0%) required hospitalization, and 58 (10.2%) 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 NIVOLUMAB. However, 567 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 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 NIVOLUMAB Alternatives Have Lower Condition aggravated Risk?

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

Related Pages

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