Does TRASTUZUMAB DERUXTECAN Cause Device defective? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device defective have been filed in association with TRASTUZUMAB DERUXTECAN (Enhertu). This represents 0.2% of all adverse event reports for TRASTUZUMAB DERUXTECAN.
5
Reports of Device defective with TRASTUZUMAB DERUXTECAN
0.2%
of all TRASTUZUMAB DERUXTECAN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device defective From TRASTUZUMAB DERUXTECAN?
Of the 5 reports.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRASTUZUMAB DERUXTECAN. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does TRASTUZUMAB DERUXTECAN Cause?
Death (384)
Off label use (258)
Nausea (251)
Myelosuppression (242)
Fatigue (186)
Malignant neoplasm progression (171)
Vomiting (140)
Diarrhoea (132)
Interstitial lung disease (130)
Pneumonitis (125)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which TRASTUZUMAB DERUXTECAN Alternatives Have Lower Device defective Risk?
TRASTUZUMAB DERUXTECAN vs TRASTUZUMAB-DKST
TRASTUZUMAB DERUXTECAN vs TRASTUZUMAB-DTTB
TRASTUZUMAB DERUXTECAN vs TRASTUZUMAB EMTANSINE
TRASTUZUMAB DERUXTECAN vs TRASTUZUMAB-PKRB
TRASTUZUMAB DERUXTECAN vs TRASTUZUMAB-QYYP