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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 Adverse event? 1,155 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,155 reports of Adverse event have been filed in association with NIVOLUMAB (OPDIVO). This represents 1.3% of all adverse event reports for NIVOLUMAB.

1,155
Reports of Adverse event with NIVOLUMAB
1.3%
of all NIVOLUMAB reports
63
Deaths
214
Hospitalizations

How Dangerous Is Adverse event From NIVOLUMAB?

Of the 1,155 reports, 63 (5.5%) resulted in death, 214 (18.5%) required hospitalization, and 37 (3.2%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NIVOLUMAB. However, 1,155 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 Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which NIVOLUMAB Alternatives Have Lower Adverse event Risk?

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

Related Pages

NIVOLUMAB Full Profile All Adverse event Reports All Drugs Causing Adverse event NIVOLUMAB Demographics