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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 C-reactive protein increased? 37 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of C-reactive protein increased have been filed in association with DURVALUMAB (IMFINZI). This represents 0.2% of all adverse event reports for DURVALUMAB.

37
Reports of C-reactive protein increased with DURVALUMAB
0.2%
of all DURVALUMAB reports
6
Deaths
22
Hospitalizations

How Dangerous Is C-reactive protein increased From DURVALUMAB?

Of the 37 reports, 6 (16.2%) resulted in death, 22 (59.5%) required hospitalization, and 2 (5.4%) were considered life-threatening.

Is C-reactive protein increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DURVALUMAB. However, 37 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 C-reactive protein increased?

METHOTREXATE (5,999) ADALIMUMAB (4,579) RITUXIMAB (4,060) ETANERCEPT (3,922) TOCILIZUMAB (3,719) INFLIXIMAB (3,621) LEFLUNOMIDE (3,574) HYDROXYCHLOROQUINE (3,552) ABATACEPT (3,451) SULFASALAZINE (3,096)

Which DURVALUMAB Alternatives Have Lower C-reactive protein increased Risk?

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

Related Pages

DURVALUMAB Full Profile All C-reactive protein increased Reports All Drugs Causing C-reactive protein increased DURVALUMAB Demographics