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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 Condition aggravated? 153 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 153 reports of Condition aggravated have been filed in association with PERTUZUMAB (PERJETA). This represents 0.7% of all adverse event reports for PERTUZUMAB.

153
Reports of Condition aggravated with PERTUZUMAB
0.7%
of all PERTUZUMAB reports
51
Deaths
108
Hospitalizations

How Dangerous Is Condition aggravated From PERTUZUMAB?

Of the 153 reports, 51 (33.3%) resulted in death, 108 (70.6%) required hospitalization, and 8 (5.2%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PERTUZUMAB. However, 153 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which PERTUZUMAB Alternatives Have Lower Condition aggravated Risk?

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

Related Pages

PERTUZUMAB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated PERTUZUMAB Demographics