Does ANAKINRA Cause Hypofibrinogenaemia? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Hypofibrinogenaemia have been filed in association with ANAKINRA (Kineret). This represents 0.1% of all adverse event reports for ANAKINRA.
9
Reports of Hypofibrinogenaemia with ANAKINRA
0.1%
of all ANAKINRA reports
0
Deaths
1
Hospitalizations
How Dangerous Is Hypofibrinogenaemia From ANAKINRA?
Of the 9 reports, 1 (11.1%) required hospitalization.
Is Hypofibrinogenaemia 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 Hypofibrinogenaemia?
METHOTREXATE (297)
PEGASPARGASE (296)
VINCRISTINE (295)
DAUNORUBICIN (186)
CYTARABINE (177)
DEXAMETHASONE (174)
HYDROCORTISONE (126)
PREDNISONE (124)
TOCILIZUMAB (121)
PREDNISOLONE (117)
Which ANAKINRA Alternatives Have Lower Hypofibrinogenaemia Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION