Does DURVALUMAB Cause Condition aggravated? 92 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 92 reports of Condition aggravated have been filed in association with DURVALUMAB (IMFINZI). This represents 0.5% of all adverse event reports for DURVALUMAB.
92
Reports of Condition aggravated with DURVALUMAB
0.5%
of all DURVALUMAB reports
18
Deaths
35
Hospitalizations
How Dangerous Is Condition aggravated From DURVALUMAB?
Of the 92 reports, 18 (19.6%) resulted in death, 35 (38.0%) required hospitalization, and 5 (5.4%) 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 DURVALUMAB. However, 92 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 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 DURVALUMAB Alternatives Have Lower Condition aggravated Risk?
DURVALUMAB vs DUTASTERIDE
DURVALUMAB vs DUTASTERIDE\TAMSULOSIN
DURVALUMAB vs DUVELISIB
DURVALUMAB vs DYDROGESTERONE
DURVALUMAB vs EBASTINE