Does CAPECITABINE Cause Intentional product use issue? 672 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 672 reports of Intentional product use issue have been filed in association with CAPECITABINE (Capecitabine). This represents 1.1% of all adverse event reports for CAPECITABINE.
672
Reports of Intentional product use issue with CAPECITABINE
1.1%
of all CAPECITABINE reports
56
Deaths
115
Hospitalizations
How Dangerous Is Intentional product use issue From CAPECITABINE?
Of the 672 reports, 56 (8.3%) resulted in death, 115 (17.1%) required hospitalization, and 9 (1.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CAPECITABINE. However, 672 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which CAPECITABINE Alternatives Have Lower Intentional product use issue Risk?
CAPECITABINE vs CAPIVASERTIB
CAPECITABINE vs CAPLACIZUMAB
CAPECITABINE vs CAPLACIZUMAB-YHDP
CAPECITABINE vs CAPMATINIB
CAPECITABINE vs CAPREOMYCIN