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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 ETRUMADENANT Cause Hypersensitivity? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Hypersensitivity have been filed in association with ETRUMADENANT. This represents 10.0% of all adverse event reports for ETRUMADENANT.

7
Reports of Hypersensitivity with ETRUMADENANT
10.0%
of all ETRUMADENANT reports
7
Deaths
7
Hospitalizations

How Dangerous Is Hypersensitivity From ETRUMADENANT?

Of the 7 reports, 7 (100.0%) resulted in death, 7 (100.0%) required hospitalization, and 7 (100.0%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ETRUMADENANT. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does ETRUMADENANT Cause?

Disease progression (19) Febrile neutropenia (16) Platelet count decreased (15) Pyrexia (14) Hyponatraemia (12) Drug hypersensitivity (11) Vomiting (11) Diarrhoea (10) Nausea (10) Acute kidney injury (7)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Related Pages

ETRUMADENANT Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity ETRUMADENANT Demographics