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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TRASTUZUMAB Cause Device breakage? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Device breakage have been filed in association with TRASTUZUMAB (Trazimera). This represents 0.0% of all adverse event reports for TRASTUZUMAB.

11
Reports of Device breakage with TRASTUZUMAB
0.0%
of all TRASTUZUMAB reports
6
Deaths
3
Hospitalizations

How Dangerous Is Device breakage From TRASTUZUMAB?

Of the 11 reports, 6 (54.5%) resulted in death, 3 (27.3%) required hospitalization.

Is Device breakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TRASTUZUMAB. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does TRASTUZUMAB Cause?

Diarrhoea (4,996) Off label use (3,802) Nausea (3,499) Fatigue (3,417) Myelosuppression (2,552) Disease progression (2,449) Death (2,378) Vomiting (2,244) Dyspnoea (2,010) Pyrexia (1,886)

What Other Drugs Cause Device breakage?

COPPER (9,201) SOMATROPIN (7,761) ETONOGESTREL (4,140) LEVONORGESTREL (2,726) ETHINYL ESTRADIOL\ETONOGESTREL (741) CARBIDOPA\LEVODOPA (634) TREPROSTINIL (396) ADALIMUMAB (375) ALBUTEROL (256) EPOPROSTENOL (240)

Which TRASTUZUMAB Alternatives Have Lower Device breakage Risk?

TRASTUZUMAB vs TRASTUZUMAB-ANNS TRASTUZUMAB vs TRASTUZUMAB DERUXTECAN TRASTUZUMAB vs TRASTUZUMAB-DKST TRASTUZUMAB vs TRASTUZUMAB-DTTB TRASTUZUMAB vs TRASTUZUMAB EMTANSINE

Related Pages

TRASTUZUMAB Full Profile All Device breakage Reports All Drugs Causing Device breakage TRASTUZUMAB Demographics