Does GEFITINIB Cause Multiple organ dysfunction syndrome? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Multiple organ dysfunction syndrome have been filed in association with GEFITINIB (Gefitinib). This represents 0.3% of all adverse event reports for GEFITINIB.
15
Reports of Multiple organ dysfunction syndrome with GEFITINIB
0.3%
of all GEFITINIB reports
14
Deaths
8
Hospitalizations
How Dangerous Is Multiple organ dysfunction syndrome From GEFITINIB?
Of the 15 reports, 14 (93.3%) resulted in death, 8 (53.3%) required hospitalization, and 3 (20.0%) 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 GEFITINIB. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does GEFITINIB Cause?
Malignant neoplasm progression (1,651)
Drug resistance (1,228)
Death (590)
Diarrhoea (393)
Rash (318)
Metastases to central nervous system (306)
Acquired gene mutation (250)
Disease progression (244)
Drug ineffective (197)
Off label use (166)
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 GEFITINIB Alternatives Have Lower Multiple organ dysfunction syndrome Risk?
GEFITINIB vs GELATIN
GEFITINIB vs GEMCITABINE
GEFITINIB vs GEMCITABINE\GEMCITABINE
GEFITINIB vs GEMFIBROZIL
GEFITINIB vs GEMTUZUMAB OZOGAMICIN