Does ANAKINRA Cause Therapy non-responder? 344 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 344 reports of Therapy non-responder have been filed in association with ANAKINRA (Kineret). This represents 2.8% of all adverse event reports for ANAKINRA.
344
Reports of Therapy non-responder with ANAKINRA
2.8%
of all ANAKINRA reports
22
Deaths
224
Hospitalizations
How Dangerous Is Therapy non-responder From ANAKINRA?
Of the 344 reports, 22 (6.4%) resulted in death, 224 (65.1%) required hospitalization, and 100 (29.1%) were considered life-threatening.
Is Therapy non-responder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 344 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 Therapy non-responder?
ETANERCEPT (3,472)
APREMILAST (3,360)
METHOTREXATE (2,965)
RITUXIMAB (2,731)
ADALIMUMAB (2,595)
PREDNISONE (2,563)
TREPROSTINIL (2,289)
INFLIXIMAB (2,122)
TOCILIZUMAB (1,775)
HYDROXYCHLOROQUINE (1,699)
Which ANAKINRA Alternatives Have Lower Therapy non-responder Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION