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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 Eosinophilia? 33 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Eosinophilia have been filed in association with ANAKINRA (Kineret). This represents 0.3% of all adverse event reports for ANAKINRA.

33
Reports of Eosinophilia with ANAKINRA
0.3%
of all ANAKINRA reports
3
Deaths
13
Hospitalizations

How Dangerous Is Eosinophilia From ANAKINRA?

Of the 33 reports, 3 (9.1%) resulted in death, 13 (39.4%) required hospitalization.

Is Eosinophilia Listed in the Official Label?

Yes, Eosinophilia is listed as a known adverse reaction in the official FDA drug label for ANAKINRA.

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 Eosinophilia?

ALBUTEROL (1,054) PREDNISONE (815) CLOZAPINE (806) MONTELUKAST (741) PANTOPRAZOLE (709) VANCOMYCIN (695) MEPOLIZUMAB (606) ALLOPURINOL (554) BUDESONIDE\FORMOTEROL (553) PIPERACILLIN\TAZOBACTAM (530)

Which ANAKINRA Alternatives Have Lower Eosinophilia Risk?

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

Related Pages

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