Does ANAKINRA Cause Post procedural infection? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Post procedural infection have been filed in association with ANAKINRA (Kineret). This represents 0.1% of all adverse event reports for ANAKINRA.
9
Reports of Post procedural infection with ANAKINRA
0.1%
of all ANAKINRA reports
0
Deaths
4
Hospitalizations
How Dangerous Is Post procedural infection From ANAKINRA?
Of the 9 reports, 4 (44.4%) required hospitalization, and 1 (11.1%) were considered life-threatening.
Is Post procedural infection Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 9 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 Post procedural infection?
ADALIMUMAB (1,109)
ETANERCEPT (362)
METHOTREXATE (226)
INFLIXIMAB (223)
UPADACITINIB (188)
TOFACITINIB (184)
GOLIMUMAB (177)
VEDOLIZUMAB (166)
RISANKIZUMAB-RZAA (157)
USTEKINUMAB (150)
Which ANAKINRA Alternatives Have Lower Post procedural infection Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION