Does ANAKINRA Cause Acute hepatic failure? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Acute hepatic failure have been filed in association with ANAKINRA (Kineret). This represents 0.1% of all adverse event reports for ANAKINRA.
6
Reports of Acute hepatic failure with ANAKINRA
0.1%
of all ANAKINRA reports
1
Deaths
4
Hospitalizations
How Dangerous Is Acute hepatic failure From ANAKINRA?
Of the 6 reports, 1 (16.7%) resulted in death, 4 (66.7%) required hospitalization, and 2 (33.3%) were considered life-threatening.
Is Acute hepatic failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 6 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 Acute hepatic failure?
ACETAMINOPHEN (3,141)
PREDNISONE (439)
IBUPROFEN (412)
RITUXIMAB (412)
CYCLOPHOSPHAMIDE (411)
DOXORUBICIN (385)
VINCRISTINE (346)
PREDNISOLONE (301)
METHOTREXATE (285)
DEXAMETHASONE (249)
Which ANAKINRA Alternatives Have Lower Acute hepatic failure Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION