High Alert
Contraindicated in:
Pregnancy
.Use Cautiously in:
Women of reproductive potential
;CV: arrhythmias, HF, hypertension, peripheral edema
Derm: alopecia, dry skin, rash, dermatitis, erythema, nail discoloration, palmar-plantar erythrodysesthesia syndrome
EENT: epistaxis, ↑lacrimation, dry eyes, rhinorrhea
Endo: hypoglycemia
F and E: hyperkalemia, hyponatremia, hypernatremia, hypokalemia
GI: ↓appetite, ↑liver enzymes, constipation, diarrhea, dyspepsia, hypoalbuminemia, nausea, stomatitis, vomiting, weight loss, abdominal pain, hemorrhoids, hyperbilirubinemia
GU: ↑serum creatinine, urinary tract infection
Hemat: anemia, leukopenia, lymphocytopenia, neutropenia, thrombocytopenia
Local: injection site pain, injection site reaction
MS: arthralgia, myalgia, muscle spasm, pain
Neuro: dizziness, dysgeusia, fatigue, headache, insomnia, paresthesia, peripheral neuropathy
Resp: cough, dyspnea, upper respiratory tract infection, ACUTE RESPIRATORY DISTRESS SYNDROME, INTERSTITIAL PNEUMONITIS, pleural effusion, PULMONARY EDEMA, PULMONARY FIBROSIS
Misc: fever, hypersensitivity reactions (including anaphylaxis and angioedema)
Drug-drug:
Neoadjuvant Treatment of Breast Cancer
Adjuvant Treatment of Breast Cancer
Metastatic Breast Cancer
Therapeutic Classification: antineoplastics
Pharmacologic Classification: HER2/neu receptor antagonists, monoclonal antibodies
Pertuzumab
Absorption: 70% absorbed following SUBQ administration.
Distribution: Minimally distributed to tissues.
Half-Life: Unknown.
Trastuzumab
Absorption: 80% absorbed following SUBQ administration.
Distribution: Minimally distributed to tissues.
Half-Life: Unknown.
(plasma concentrations)
| ROUTE | ONSET | PEAK | DURATION |
|---|---|---|---|
| Pertuzumab (SUBQ) | unknown | 4 days | unknown |
| Trastuzumab (SUBQ) | unknown | 4 days | unknown |
Advise patient to notify health care provider immediately if signs and symptoms of cardiomyopathy (new onset or worsening shortness of breath, cough, swelling of ankles or legs, swelling of face, palpitations, weight gain >5 pounds in 24 hr, dizziness, loss of consciousness) or pulmonary toxicity (shortness of breath or wheezing) occur.
May cause fetal harm. Advise women of reproductive potential to use effective contraception and to avoid breastfeeding for 7 mo after last dose. If Phesgo is administered during pregnancy or if a patient becomes pregnant while receiving Phesgo or within 7 mo following last dose of Phesgo, health care providers and patients should immediately report exposure to pharmacovigilance program at Genentech at 1-888-835-2555.