Does CAPECITABINE Cause Condition aggravated? 339 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 339 reports of Condition aggravated have been filed in association with CAPECITABINE (Capecitabine). This represents 0.5% of all adverse event reports for CAPECITABINE.
339
Reports of Condition aggravated with CAPECITABINE
0.5%
of all CAPECITABINE reports
75
Deaths
145
Hospitalizations
How Dangerous Is Condition aggravated From CAPECITABINE?
Of the 339 reports, 75 (22.1%) resulted in death, 145 (42.8%) required hospitalization, and 29 (8.6%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CAPECITABINE. However, 339 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CAPECITABINE Alternatives Have Lower Condition aggravated Risk?
CAPECITABINE vs CAPIVASERTIB
CAPECITABINE vs CAPLACIZUMAB
CAPECITABINE vs CAPLACIZUMAB-YHDP
CAPECITABINE vs CAPMATINIB
CAPECITABINE vs CAPREOMYCIN