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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 RETIFANLIMAB Cause Condition aggravated? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Condition aggravated have been filed in association with RETIFANLIMAB (ZYNYZ). This represents 9.4% of all adverse event reports for RETIFANLIMAB.

9
Reports of Condition aggravated with RETIFANLIMAB
9.4%
of all RETIFANLIMAB reports
6
Deaths
9
Hospitalizations

How Dangerous Is Condition aggravated From RETIFANLIMAB?

Of the 9 reports, 6 (66.7%) resulted in death, 9 (100.0%) required hospitalization, and 1 (11.1%) 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 RETIFANLIMAB. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does RETIFANLIMAB Cause?

Diarrhoea (23) Nausea (14) Neutrophil count decreased (12) White blood cell count decreased (12) Disease progression (11) Neutropenic sepsis (11) Pulmonary embolism (9) Pyrexia (9) Asthenia (8) Blood sodium decreased (8)

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)

Related Pages

RETIFANLIMAB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated RETIFANLIMAB Demographics