Does ANAKINRA Cause Product use issue? 340 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 340 reports of Product use issue have been filed in association with ANAKINRA (Kineret). This represents 2.8% of all adverse event reports for ANAKINRA.
340
Reports of Product use issue with ANAKINRA
2.8%
of all ANAKINRA reports
22
Deaths
196
Hospitalizations
How Dangerous Is Product use issue From ANAKINRA?
Of the 340 reports, 22 (6.5%) resulted in death, 196 (57.6%) required hospitalization, and 49 (14.4%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 340 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ANAKINRA Alternatives Have Lower Product use issue Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION