Does ANAKINRA Cause Ill-defined disorder? 409 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 409 reports of Ill-defined disorder have been filed in association with ANAKINRA (Kineret). This represents 3.4% of all adverse event reports for ANAKINRA.
409
Reports of Ill-defined disorder with ANAKINRA
3.4%
of all ANAKINRA reports
6
Deaths
135
Hospitalizations
How Dangerous Is Ill-defined disorder From ANAKINRA?
Of the 409 reports, 6 (1.5%) resulted in death, 135 (33.0%) required hospitalization, and 7 (1.7%) were considered life-threatening.
Is Ill-defined disorder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 409 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 Ill-defined disorder?
ACETAMINOPHEN\OXYCODONE (9,780)
ACETAMINOPHEN\HYDROCODONE (6,159)
TOCILIZUMAB (4,411)
RITUXIMAB (4,220)
ETANERCEPT (4,202)
METHOTREXATE (4,063)
ABATACEPT (3,630)
LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN (3,600)
LEFLUNOMIDE (3,570)
CERTOLIZUMAB PEGOL (3,273)
Which ANAKINRA Alternatives Have Lower Ill-defined disorder Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION