Does ANAKINRA Cause Condition aggravated? 1,339 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,339 reports of Condition aggravated have been filed in association with ANAKINRA (Kineret). This represents 11.0% of all adverse event reports for ANAKINRA.
1,339
Reports of Condition aggravated with ANAKINRA
11.0%
of all ANAKINRA reports
56
Deaths
718
Hospitalizations
How Dangerous Is Condition aggravated From ANAKINRA?
Of the 1,339 reports, 56 (4.2%) resulted in death, 718 (53.6%) required hospitalization, and 113 (8.4%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 1,339 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)
Rheumatoid arthritis (1,300)
Drug intolerance (946)
Joint swelling (921)
Injection site pain (879)
Product dose omission issue (864)
Arthralgia (850)
Pyrexia (782)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ANAKINRA Alternatives Have Lower Condition aggravated Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION