Does CAPECITABINE Cause Unevaluable event? 195 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 195 reports of Unevaluable event have been filed in association with CAPECITABINE (Capecitabine). This represents 0.3% of all adverse event reports for CAPECITABINE.
195
Reports of Unevaluable event with CAPECITABINE
0.3%
of all CAPECITABINE reports
8
Deaths
64
Hospitalizations
How Dangerous Is Unevaluable event From CAPECITABINE?
Of the 195 reports, 8 (4.1%) resulted in death, 64 (32.8%) required hospitalization, and 2 (1.0%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CAPECITABINE. However, 195 reports have been filed with the FAERS database.
What Other Side Effects Does CAPECITABINE Cause?
Diarrhoea (9,277)
Nausea (6,248)
Palmar-plantar erythrodysaesthesia syndrome (5,294)
Fatigue (5,018)
Death (4,422)
Vomiting (4,111)
Disease progression (3,808)
Off label use (3,193)
Malignant neoplasm progression (2,425)
Asthenia (2,352)
What Other Drugs Cause Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which CAPECITABINE Alternatives Have Lower Unevaluable event Risk?
CAPECITABINE vs CAPIVASERTIB
CAPECITABINE vs CAPLACIZUMAB
CAPECITABINE vs CAPLACIZUMAB-YHDP
CAPECITABINE vs CAPMATINIB
CAPECITABINE vs CAPREOMYCIN