Does BORTEZOMIB Cause Fibrin d dimer increased? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Fibrin d dimer increased have been filed in association with BORTEZOMIB (bortezomib). This represents 0.0% of all adverse event reports for BORTEZOMIB.
12
Reports of Fibrin d dimer increased with BORTEZOMIB
0.0%
of all BORTEZOMIB reports
2
Deaths
11
Hospitalizations
How Dangerous Is Fibrin d dimer increased From BORTEZOMIB?
Of the 12 reports, 2 (16.7%) resulted in death, 11 (91.7%) required hospitalization, and 2 (16.7%) 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 BORTEZOMIB. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does BORTEZOMIB Cause?
Plasma cell myeloma (6,683)
Off label use (4,754)
Neuropathy peripheral (4,067)
Drug ineffective (2,730)
Diarrhoea (2,244)
Thrombocytopenia (2,082)
Death (2,025)
Pneumonia (2,020)
Fatigue (1,757)
Neutropenia (1,530)
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 BORTEZOMIB Alternatives Have Lower Fibrin d dimer increased Risk?
BORTEZOMIB vs BOSENTAN
BORTEZOMIB vs BOSENTAN\BOSENTAN
BORTEZOMIB vs BOSULIF
BORTEZOMIB vs BOSUTINIB
BORTEZOMIB vs BOTOX