Does TUCATINIB Cause Intentional product misuse? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Intentional product misuse have been filed in association with TUCATINIB (TUKYSA). This represents 0.2% of all adverse event reports for TUCATINIB.
14
Reports of Intentional product misuse with TUCATINIB
0.2%
of all TUCATINIB reports
2
Deaths
2
Hospitalizations
How Dangerous Is Intentional product misuse From TUCATINIB?
Of the 14 reports, 2 (14.3%) resulted in death, 2 (14.3%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TUCATINIB. However, 14 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 misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which TUCATINIB Alternatives Have Lower Intentional product misuse Risk?
TUCATINIB vs TUCIDINOSTAT
TUCATINIB vs TYKERB
TUCATINIB vs TYLENOL
TUCATINIB vs TYROTHRICIN
TUCATINIB vs TYSABRI