Does ANAKINRA Cause Intentional product use issue? 393 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 393 reports of Intentional product use issue have been filed in association with ANAKINRA (Kineret). This represents 3.2% of all adverse event reports for ANAKINRA.
393
Reports of Intentional product use issue with ANAKINRA
3.2%
of all ANAKINRA reports
92
Deaths
304
Hospitalizations
How Dangerous Is Intentional product use issue From ANAKINRA?
Of the 393 reports, 92 (23.4%) resulted in death, 304 (77.4%) required hospitalization, and 191 (48.6%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 393 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ANAKINRA Alternatives Have Lower Intentional product use issue Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION