Does GEMCITABINE Cause Fibrin d dimer increased? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Fibrin d dimer increased have been filed in association with GEMCITABINE (Gemcitabine). This represents 0.0% of all adverse event reports for GEMCITABINE.
8
Reports of Fibrin d dimer increased with GEMCITABINE
0.0%
of all GEMCITABINE reports
1
Deaths
3
Hospitalizations
How Dangerous Is Fibrin d dimer increased From GEMCITABINE?
Of the 8 reports, 1 (12.5%) resulted in death, 3 (37.5%) required hospitalization, and 1 (12.5%) 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 GEMCITABINE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does GEMCITABINE Cause?
Off label use (3,319)
Disease progression (3,123)
Thrombocytopenia (2,320)
Drug ineffective (2,003)
Malignant neoplasm progression (1,962)
Neutropenia (1,892)
Anaemia (1,745)
Pyrexia (1,511)
Nausea (1,336)
Myelosuppression (1,197)
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 GEMCITABINE Alternatives Have Lower Fibrin d dimer increased Risk?
GEMCITABINE vs GEMCITABINE\GEMCITABINE
GEMCITABINE vs GEMFIBROZIL
GEMCITABINE vs GEMTUZUMAB OZOGAMICIN
GEMCITABINE vs GEMZAR
GEMCITABINE vs GENTAMICIN