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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 Hypersensitivity? 299 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 299 reports of Hypersensitivity have been filed in association with ANAKINRA (Kineret). This represents 2.5% of all adverse event reports for ANAKINRA.

299
Reports of Hypersensitivity with ANAKINRA
2.5%
of all ANAKINRA reports
9
Deaths
126
Hospitalizations

How Dangerous Is Hypersensitivity From ANAKINRA?

Of the 299 reports, 9 (3.0%) resulted in death, 126 (42.1%) required hospitalization, and 17 (5.7%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity 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 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)

Which ANAKINRA Alternatives Have Lower Hypersensitivity Risk?

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

Related Pages

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