Does ANAKINRA Cause Device issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device issue have been filed in association with ANAKINRA (Kineret). This represents 0.0% of all adverse event reports for ANAKINRA.
5
Reports of Device issue with ANAKINRA
0.0%
of all ANAKINRA reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device issue From ANAKINRA?
Of the 5 reports, 2 (40.0%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 5 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 Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ANAKINRA Alternatives Have Lower Device issue Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION