Does ANAKINRA Cause Multiple organ dysfunction syndrome? 111 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 111 reports of Multiple organ dysfunction syndrome have been filed in association with ANAKINRA (Kineret). This represents 0.9% of all adverse event reports for ANAKINRA.
111
Reports of Multiple organ dysfunction syndrome with ANAKINRA
0.9%
of all ANAKINRA reports
99
Deaths
61
Hospitalizations
How Dangerous Is Multiple organ dysfunction syndrome From ANAKINRA?
Of the 111 reports, 99 (89.2%) resulted in death, 61 (55.0%) required hospitalization, and 28 (25.2%) were considered life-threatening.
Is Multiple organ dysfunction syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 111 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 Multiple organ dysfunction syndrome?
TACROLIMUS (1,847)
CYCLOPHOSPHAMIDE (1,597)
MYCOPHENOLATE MOFETIL (1,566)
PREDNISONE (1,525)
DEXAMETHASONE (1,355)
METHOTREXATE (1,317)
METHYLPREDNISOLONE (1,278)
RITUXIMAB (1,188)
PREDNISOLONE (1,154)
CYCLOSPORINE (933)
Which ANAKINRA Alternatives Have Lower Multiple organ dysfunction syndrome Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION