Does NIVOLUMAB Cause Incorrect product storage? 176 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 176 reports of Incorrect product storage have been filed in association with NIVOLUMAB (OPDIVO). This represents 0.2% of all adverse event reports for NIVOLUMAB.
176
Reports of Incorrect product storage with NIVOLUMAB
0.2%
of all NIVOLUMAB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From NIVOLUMAB?
Of the 176 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NIVOLUMAB. However, 176 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which NIVOLUMAB Alternatives Have Lower Incorrect product storage Risk?
NIVOLUMAB vs NIVOLUMAB\RELATLIMAB-RMBW
NIVOLUMAB vs NIZATIDINE
NIVOLUMAB vs NOMEGESTROL
NIVOLUMAB vs NORDAZEPAM
NIVOLUMAB vs NOREPINEPHRINE