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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 LESTAURTINIB Cause Sepsis? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Sepsis have been filed in association with LESTAURTINIB. This represents 11.3% of all adverse event reports for LESTAURTINIB.

9
Reports of Sepsis with LESTAURTINIB
11.3%
of all LESTAURTINIB reports
0
Deaths
9
Hospitalizations

How Dangerous Is Sepsis From LESTAURTINIB?

Of the 9 reports, 9 (100.0%) required hospitalization, and 8 (88.9%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LESTAURTINIB. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does LESTAURTINIB Cause?

Febrile neutropenia (23) Hypertriglyceridaemia (13) Clostridium difficile colitis (10) Death (10) Diarrhoea (10) Enterococcal infection (9) Bronchiolitis (8) Candida infection (8) Hypertension (8) Klebsiella infection (8)

What Other Drugs Cause Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Related Pages

LESTAURTINIB Full Profile All Sepsis Reports All Drugs Causing Sepsis LESTAURTINIB Demographics