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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 Adverse event? 74 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 74 reports of Adverse event have been filed in association with ANAKINRA (Kineret). This represents 0.6% of all adverse event reports for ANAKINRA.

74
Reports of Adverse event with ANAKINRA
0.6%
of all ANAKINRA reports
7
Deaths
24
Hospitalizations

How Dangerous Is Adverse event From ANAKINRA?

Of the 74 reports, 7 (9.5%) resulted in death, 24 (32.4%) required hospitalization, and 6 (8.1%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

Yes, Adverse event 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 Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which ANAKINRA Alternatives Have Lower Adverse event Risk?

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

Related Pages

ANAKINRA Full Profile All Adverse event Reports All Drugs Causing Adverse event ANAKINRA Demographics