Does TUCATINIB Cause Adverse event? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Adverse event have been filed in association with TUCATINIB (TUKYSA). This represents 0.3% of all adverse event reports for TUCATINIB.
20
Reports of Adverse event with TUCATINIB
0.3%
of all TUCATINIB reports
1
Deaths
6
Hospitalizations
How Dangerous Is Adverse event From TUCATINIB?
Of the 20 reports, 1 (5.0%) resulted in death, 6 (30.0%) required hospitalization, and 1 (5.0%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TUCATINIB. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does TUCATINIB Cause?
Diarrhoea (1,587)
Nausea (862)
Fatigue (843)
Vomiting (483)
Death (400)
Off label use (392)
Malignant neoplasm progression (361)
Palmar-plantar erythrodysaesthesia syndrome (355)
Product dose omission issue (332)
Asthenia (322)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which TUCATINIB Alternatives Have Lower Adverse event Risk?
TUCATINIB vs TUCIDINOSTAT
TUCATINIB vs TYKERB
TUCATINIB vs TYLENOL
TUCATINIB vs TYROTHRICIN
TUCATINIB vs TYSABRI