Does TUCATINIB Cause Product dose omission in error? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Product dose omission in error have been filed in association with TUCATINIB (TUKYSA). This represents 0.7% of all adverse event reports for TUCATINIB.
43
Reports of Product dose omission in error with TUCATINIB
0.7%
of all TUCATINIB reports
1
Deaths
17
Hospitalizations
How Dangerous Is Product dose omission in error From TUCATINIB?
Of the 43 reports, 1 (2.3%) resulted in death, 17 (39.5%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TUCATINIB. However, 43 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 Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which TUCATINIB Alternatives Have Lower Product dose omission in error Risk?
TUCATINIB vs TUCIDINOSTAT
TUCATINIB vs TYKERB
TUCATINIB vs TYLENOL
TUCATINIB vs TYROTHRICIN
TUCATINIB vs TYSABRI