Does PERTUZUMAB Cause Intentional product use issue? 239 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 239 reports of Intentional product use issue have been filed in association with PERTUZUMAB (PERJETA). This represents 1.1% of all adverse event reports for PERTUZUMAB.
239
Reports of Intentional product use issue with PERTUZUMAB
1.1%
of all PERTUZUMAB reports
38
Deaths
81
Hospitalizations
How Dangerous Is Intentional product use issue From PERTUZUMAB?
Of the 239 reports, 38 (15.9%) resulted in death, 81 (33.9%) required hospitalization, and 3 (1.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PERTUZUMAB. However, 239 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which PERTUZUMAB Alternatives Have Lower Intentional product use issue Risk?
PERTUZUMAB vs PERTUZUMAB\TRASTUZUMAB
PERTUZUMAB vs PETROLATUM
PERTUZUMAB vs PEVONEDISTAT
PERTUZUMAB vs PEXIDARTINIB
PERTUZUMAB vs PHENACETIN