Does ANAKINRA Cause Intentional product misuse? 267 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 267 reports of Intentional product misuse have been filed in association with ANAKINRA (Kineret). This represents 2.2% of all adverse event reports for ANAKINRA.
267
Reports of Intentional product misuse with ANAKINRA
2.2%
of all ANAKINRA reports
6
Deaths
46
Hospitalizations
How Dangerous Is Intentional product misuse From ANAKINRA?
Of the 267 reports, 6 (2.2%) resulted in death, 46 (17.2%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 267 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 misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which ANAKINRA Alternatives Have Lower Intentional product misuse Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION