Does ANAKINRA Cause Off label use? 4,317 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,317 reports of Off label use have been filed in association with ANAKINRA (Kineret). This represents 35.6% of all adverse event reports for ANAKINRA.
4,317
Reports of Off label use with ANAKINRA
35.6%
of all ANAKINRA reports
413
Deaths
1,517
Hospitalizations
How Dangerous Is Off label use From ANAKINRA?
Of the 4,317 reports, 413 (9.6%) resulted in death, 1,517 (35.1%) required hospitalization, and 415 (9.6%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 4,317 reports have been filed with the FAERS database.
What Other Side Effects Does ANAKINRA Cause?
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)
Pyrexia (782)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which ANAKINRA Alternatives Have Lower Off label use Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION