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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CAPECITABINE Cause Performance status decreased? 75 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 75 reports of Performance status decreased have been filed in association with CAPECITABINE (Capecitabine). This represents 0.1% of all adverse event reports for CAPECITABINE.

75
Reports of Performance status decreased with CAPECITABINE
0.1%
of all CAPECITABINE reports
19
Deaths
38
Hospitalizations

How Dangerous Is Performance status decreased From CAPECITABINE?

Of the 75 reports, 19 (25.3%) resulted in death, 38 (50.7%) required hospitalization, and 3 (4.0%) were considered life-threatening.

Is Performance status decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CAPECITABINE. However, 75 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 Performance status decreased?

BACLOFEN (156) LENALIDOMIDE (118) PACLITAXEL (112) BEVACIZUMAB (103) SODIUM OXYBATE (103) CARBOPLATIN (100) DEXAMETHASONE (80) NIRAPARIB (75) LUMATEPERONE (68) NIVOLUMAB (65)

Which CAPECITABINE Alternatives Have Lower Performance status decreased Risk?

CAPECITABINE vs CAPIVASERTIB CAPECITABINE vs CAPLACIZUMAB CAPECITABINE vs CAPLACIZUMAB-YHDP CAPECITABINE vs CAPMATINIB CAPECITABINE vs CAPREOMYCIN

Related Pages

CAPECITABINE Full Profile All Performance status decreased Reports All Drugs Causing Performance status decreased CAPECITABINE Demographics