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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 ANAKINRA Cause Sepsis? 362 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 362 reports of Sepsis have been filed in association with ANAKINRA (Kineret). This represents 3.0% of all adverse event reports for ANAKINRA.

362
Reports of Sepsis with ANAKINRA
3.0%
of all ANAKINRA reports
122
Deaths
267
Hospitalizations

How Dangerous Is Sepsis From ANAKINRA?

Of the 362 reports, 122 (33.7%) resulted in death, 267 (73.8%) required hospitalization, and 208 (57.5%) 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 ANAKINRA. However, 362 reports have been filed with the FAERS database.

What Other Side Effects Does ANAKINRA Cause?

Off label use (4,317) Drug ineffective (3,368) Pain (1,344) Condition aggravated (1,339) Rheumatoid arthritis (1,300) Drug intolerance (946) Joint swelling (921) Injection site pain (879) Product dose omission issue (864) Arthralgia (850)

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)

Which ANAKINRA Alternatives Have Lower Sepsis Risk?

ANAKINRA vs ANAMORELIN ANAKINRA vs ANASTROZOLE ANAKINRA vs ANDEXANET ALFA ANAKINRA vs ANDROGEL ANAKINRA vs ANETHOLTRITHION

Related Pages

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