Does CAPECITABINE Cause Product use issue? 199 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 199 reports of Product use issue have been filed in association with CAPECITABINE (Capecitabine). This represents 0.3% of all adverse event reports for CAPECITABINE.
199
Reports of Product use issue with CAPECITABINE
0.3%
of all CAPECITABINE reports
45
Deaths
62
Hospitalizations
How Dangerous Is Product use issue From CAPECITABINE?
Of the 199 reports, 45 (22.6%) resulted in death, 62 (31.2%) required hospitalization, and 6 (3.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CAPECITABINE. However, 199 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which CAPECITABINE Alternatives Have Lower Product use issue Risk?
CAPECITABINE vs CAPIVASERTIB
CAPECITABINE vs CAPLACIZUMAB
CAPECITABINE vs CAPLACIZUMAB-YHDP
CAPECITABINE vs CAPMATINIB
CAPECITABINE vs CAPREOMYCIN