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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 Drug hypersensitivity? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Drug hypersensitivity have been filed in association with ETRUMADENANT. This represents 15.7% of all adverse event reports for ETRUMADENANT.

11
Reports of Drug hypersensitivity with ETRUMADENANT
15.7%
of all ETRUMADENANT reports
9
Deaths
11
Hospitalizations

How Dangerous Is Drug hypersensitivity From ETRUMADENANT?

Of the 11 reports, 9 (81.8%) resulted in death, 11 (100.0%) required hospitalization, and 8 (72.7%) were considered life-threatening.

Is Drug hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ETRUMADENANT. However, 11 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) Vomiting (11) Diarrhoea (10) Nausea (10) Acute kidney injury (7) Fungal infection (7)

What Other Drugs Cause Drug hypersensitivity?

METHOTREXATE (16,677) ETANERCEPT (12,991) ADALIMUMAB (11,599) MORPHINE (11,095) RITUXIMAB (8,924) LEFLUNOMIDE (8,148) INFLIXIMAB (8,119) TOCILIZUMAB (7,883) ABATACEPT (7,808) CODEINE (7,479)

Related Pages

ETRUMADENANT Full Profile All Drug hypersensitivity Reports All Drugs Causing Drug hypersensitivity ETRUMADENANT Demographics