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PERJETA® (pertuzumab)
Required Testing Prior to Administration
 ECHO: Due to risk of heart failure, every patient must have a baseline left ventricular ejection
fraction (LVEF). Do not administer if LVEF < 45%, or LVEF 45% to 49% with ≥ 10% absolute
decrease below pretreatment values
 In females of childbearing age: pregnancy test
IV Administration
 DO NOT mix with other drugs
 DO NOT dilute with D5W
 ONLY use in normal saline – sodium chloride 0.9%
 DO NOT use at Y-site
 Invert bag gently to mix; DO NOT shake
 Administer immediately after preparation, or store for up to 24 hours at 2 to 8 degrees C
 DO NOT give as an IV push or IV bolus
 Only give as an IV infusion: 840-mg dose over 60 minutes OR 420-mg dose over 30 to 60
minutes
 Dilute the desired dose in a PVC or non-PVC polyolefin infusion bag/tubing containing 250 mL
NS
 Order of Administration:
o Docetaxel must always be administered LAST, but either pertuzumab or trastuzumab
can be given first or second.
o Pertuzumab must be given at least 30 minutes prior to DOCETAXEL
o Observe patient for 30 to 60 minutes following pertuzumab infusion before
administering the next medication
Common Side Effects
 Nausea
 Diarrhea
 Neutropenia
 Fatigue
 Rash
 Peripheral neuropathy
 Hair loss
Monitoring
 Cardiac symptoms – monitor vital signs, fluid status, and assess for dyspnea
 LVEF – baseline, every 3 months for metastatic use or every 6 weeks in neoadjuvant use
 Infusion reactions - 60 minutes after first infusion and 30 minutes after subsequent infusions.
Depending on severity, infusion may need to be slowed, interrupted or discontinued completely.
Symptoms of infusion reactions include: fever, chills, fatigue, headache, hypersensitivity and
vomiting.
o Anaphylaxis treatment: MILD: Anti-histamines. SEVERE: Airway management,
epinephrine, cardiac monitoring, IV fluids

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Pertuzumab Nursing Educational Pamphlet

  • 1. PERJETA® (pertuzumab) Required Testing Prior to Administration  ECHO: Due to risk of heart failure, every patient must have a baseline left ventricular ejection fraction (LVEF). Do not administer if LVEF < 45%, or LVEF 45% to 49% with ≥ 10% absolute decrease below pretreatment values  In females of childbearing age: pregnancy test IV Administration  DO NOT mix with other drugs  DO NOT dilute with D5W  ONLY use in normal saline – sodium chloride 0.9%  DO NOT use at Y-site  Invert bag gently to mix; DO NOT shake  Administer immediately after preparation, or store for up to 24 hours at 2 to 8 degrees C  DO NOT give as an IV push or IV bolus  Only give as an IV infusion: 840-mg dose over 60 minutes OR 420-mg dose over 30 to 60 minutes  Dilute the desired dose in a PVC or non-PVC polyolefin infusion bag/tubing containing 250 mL NS  Order of Administration: o Docetaxel must always be administered LAST, but either pertuzumab or trastuzumab can be given first or second. o Pertuzumab must be given at least 30 minutes prior to DOCETAXEL o Observe patient for 30 to 60 minutes following pertuzumab infusion before administering the next medication Common Side Effects  Nausea  Diarrhea  Neutropenia  Fatigue  Rash  Peripheral neuropathy  Hair loss Monitoring  Cardiac symptoms – monitor vital signs, fluid status, and assess for dyspnea  LVEF – baseline, every 3 months for metastatic use or every 6 weeks in neoadjuvant use  Infusion reactions - 60 minutes after first infusion and 30 minutes after subsequent infusions. Depending on severity, infusion may need to be slowed, interrupted or discontinued completely. Symptoms of infusion reactions include: fever, chills, fatigue, headache, hypersensitivity and vomiting. o Anaphylaxis treatment: MILD: Anti-histamines. SEVERE: Airway management, epinephrine, cardiac monitoring, IV fluids