Does TOCILIZUMAB Cause Fibrin d dimer increased? 44 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 44 reports of Fibrin d dimer increased have been filed in association with TOCILIZUMAB (Tocilizumab-anoh). This represents 0.0% of all adverse event reports for TOCILIZUMAB.
44
Reports of Fibrin d dimer increased with TOCILIZUMAB
0.0%
of all TOCILIZUMAB reports
19
Deaths
20
Hospitalizations
How Dangerous Is Fibrin d dimer increased From TOCILIZUMAB?
Of the 44 reports, 19 (43.2%) resulted in death, 20 (45.5%) required hospitalization, and 8 (18.2%) were considered life-threatening.
Is Fibrin d dimer increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOCILIZUMAB. However, 44 reports have been filed with the FAERS database.
What Other Side Effects Does TOCILIZUMAB Cause?
Drug ineffective (32,342)
Rheumatoid arthritis (20,652)
Pain (18,384)
Off label use (18,256)
Arthralgia (15,536)
Joint swelling (14,831)
Fatigue (13,802)
Rash (12,327)
Drug intolerance (11,952)
Contraindicated product administered (11,547)
What Other Drugs Cause Fibrin d dimer increased?
ADALIMUMAB (97)
RIVAROXABAN (91)
PREDNISONE (69)
RITUXIMAB (63)
APIXABAN (59)
ASPIRIN (54)
ACETAMINOPHEN (53)
LENALIDOMIDE (53)
METHOTREXATE (52)
BAMLANIVIMAB (49)
Which TOCILIZUMAB Alternatives Have Lower Fibrin d dimer increased Risk?
TOCILIZUMAB vs TOCILIZUMAB-AAZG
TOCILIZUMAB vs TOCOPHEROL
TOCILIZUMAB vs TOFACITINIB
TOCILIZUMAB vs TOFERSEN
TOCILIZUMAB vs TOLNAFTATE