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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 DURVALUMAB Cause Unevaluable event? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Unevaluable event have been filed in association with DURVALUMAB (IMFINZI). This represents 0.1% of all adverse event reports for DURVALUMAB.

8
Reports of Unevaluable event with DURVALUMAB
0.1%
of all DURVALUMAB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Unevaluable event From DURVALUMAB?

Of the 8 reports, 1 (12.5%) required hospitalization.

Is Unevaluable event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DURVALUMAB. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does DURVALUMAB Cause?

Death (2,817) Malignant neoplasm progression (1,330) Pneumonitis (827) Radiation pneumonitis (786) Pyrexia (573) Diarrhoea (530) Pneumonia (453) Dyspnoea (444) Interstitial lung disease (430) Off label use (395)

What Other Drugs Cause Unevaluable event?

ADALIMUMAB (4,242) ETANERCEPT (3,902) LENALIDOMIDE (3,331) OXYCODONE (3,145) AMBRISENTAN (2,336) SODIUM OXYBATE (2,328) CARBIDOPA\LEVODOPA (1,632) DUPILUMAB (1,410) MORPHINE (1,161) ACETAMINOPHEN\HYDROCODONE (1,118)

Which DURVALUMAB Alternatives Have Lower Unevaluable event Risk?

DURVALUMAB vs DUTASTERIDE DURVALUMAB vs DUTASTERIDE\TAMSULOSIN DURVALUMAB vs DUVELISIB DURVALUMAB vs DYDROGESTERONE DURVALUMAB vs EBASTINE

Related Pages

DURVALUMAB Full Profile All Unevaluable event Reports All Drugs Causing Unevaluable event DURVALUMAB Demographics