Does GEMCITABINE Cause Multiple organ dysfunction syndrome? 158 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 158 reports of Multiple organ dysfunction syndrome have been filed in association with GEMCITABINE (Gemcitabine). This represents 0.5% of all adverse event reports for GEMCITABINE.
158
Reports of Multiple organ dysfunction syndrome with GEMCITABINE
0.5%
of all GEMCITABINE reports
132
Deaths
86
Hospitalizations
How Dangerous Is Multiple organ dysfunction syndrome From GEMCITABINE?
Of the 158 reports, 132 (83.5%) resulted in death, 86 (54.4%) required hospitalization, and 43 (27.2%) were considered life-threatening.
Is Multiple organ dysfunction syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GEMCITABINE. However, 158 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 Multiple organ dysfunction syndrome?
TACROLIMUS (1,847)
CYCLOPHOSPHAMIDE (1,597)
MYCOPHENOLATE MOFETIL (1,566)
PREDNISONE (1,525)
DEXAMETHASONE (1,355)
METHOTREXATE (1,317)
METHYLPREDNISOLONE (1,278)
RITUXIMAB (1,188)
PREDNISOLONE (1,154)
CYCLOSPORINE (933)
Which GEMCITABINE Alternatives Have Lower Multiple organ dysfunction syndrome Risk?
GEMCITABINE vs GEMCITABINE\GEMCITABINE
GEMCITABINE vs GEMFIBROZIL
GEMCITABINE vs GEMTUZUMAB OZOGAMICIN
GEMCITABINE vs GEMZAR
GEMCITABINE vs GENTAMICIN