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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 PERTUZUMAB Cause Device breakage? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device breakage have been filed in association with PERTUZUMAB (PERJETA). This represents 0.0% of all adverse event reports for PERTUZUMAB.

8
Reports of Device breakage with PERTUZUMAB
0.0%
of all PERTUZUMAB reports
6
Deaths
2
Hospitalizations

How Dangerous Is Device breakage From PERTUZUMAB?

Of the 8 reports, 6 (75.0%) resulted in death, 2 (25.0%) required hospitalization.

Is Device breakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PERTUZUMAB. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does PERTUZUMAB Cause?

Diarrhoea (3,343) Off label use (1,886) Fatigue (1,672) Nausea (1,669) Myelosuppression (1,311) Disease progression (1,142) Vomiting (1,096) Dyspnoea (987) Neuropathy peripheral (983) Pyrexia (926)

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 PERTUZUMAB Alternatives Have Lower Device breakage Risk?

PERTUZUMAB vs PERTUZUMAB\TRASTUZUMAB PERTUZUMAB vs PETROLATUM PERTUZUMAB vs PEVONEDISTAT PERTUZUMAB vs PEXIDARTINIB PERTUZUMAB vs PHENACETIN

Related Pages

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