Does TUCATINIB Cause Intentional product use issue? 68 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Intentional product use issue have been filed in association with TUCATINIB (TUKYSA). This represents 1.1% of all adverse event reports for TUCATINIB.
68
Reports of Intentional product use issue with TUCATINIB
1.1%
of all TUCATINIB reports
6
Deaths
35
Hospitalizations
How Dangerous Is Intentional product use issue From TUCATINIB?
Of the 68 reports, 6 (8.8%) resulted in death, 35 (51.5%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TUCATINIB. However, 68 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 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 TUCATINIB Alternatives Have Lower Intentional product use issue Risk?
TUCATINIB vs TUCIDINOSTAT
TUCATINIB vs TYKERB
TUCATINIB vs TYLENOL
TUCATINIB vs TYROTHRICIN
TUCATINIB vs TYSABRI