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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 Performance status decreased? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Performance status decreased have been filed in association with DURVALUMAB (IMFINZI). This represents 0.1% of all adverse event reports for DURVALUMAB.

16
Reports of Performance status decreased with DURVALUMAB
0.1%
of all DURVALUMAB reports
5
Deaths
7
Hospitalizations

How Dangerous Is Performance status decreased From DURVALUMAB?

Of the 16 reports, 5 (31.3%) resulted in death, 7 (43.8%) required hospitalization, and 1 (6.3%) were considered life-threatening.

Is Performance status decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DURVALUMAB. However, 16 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 Performance status decreased?

BACLOFEN (156) LENALIDOMIDE (118) PACLITAXEL (112) BEVACIZUMAB (103) SODIUM OXYBATE (103) CARBOPLATIN (100) DEXAMETHASONE (80) CAPECITABINE (75) NIRAPARIB (75) LUMATEPERONE (68)

Which DURVALUMAB Alternatives Have Lower Performance status decreased Risk?

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

Related Pages

DURVALUMAB Full Profile All Performance status decreased Reports All Drugs Causing Performance status decreased DURVALUMAB Demographics