Does GEFITINIB Cause Performance status decreased? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Performance status decreased have been filed in association with GEFITINIB (Gefitinib). This represents 0.2% of all adverse event reports for GEFITINIB.
7
Reports of Performance status decreased with GEFITINIB
0.2%
of all GEFITINIB reports
3
Deaths
1
Hospitalizations
How Dangerous Is Performance status decreased From GEFITINIB?
Of the 7 reports, 3 (42.9%) resulted in death, 1 (14.3%) required hospitalization.
Is Performance status decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GEFITINIB. However, 7 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 Performance status decreased?
BACLOFEN (156)
LENALIDOMIDE (118)
PACLITAXEL (112)
BEVACIZUMAB (103)
SODIUM OXYBATE (103)
CARBOPLATIN (100)
DEXAMETHASONE (80)
CAPECITABINE (75)
NIRAPARIB (75)
LUMATEPERONE (68)
Which GEFITINIB Alternatives Have Lower Performance status decreased Risk?
GEFITINIB vs GELATIN
GEFITINIB vs GEMCITABINE
GEFITINIB vs GEMCITABINE\GEMCITABINE
GEFITINIB vs GEMFIBROZIL
GEFITINIB vs GEMTUZUMAB OZOGAMICIN