Kanjinti, illustration of injection vial form (not a photo of the actual pack)

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Kanjinti

Trastuzumab

Prescription required

$1800.00

420mg · 1 vial

BrandBranded medicine· By Amgen

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FDA boxed warningCardiomyopathy, infusion reactions, embryo-fetal toxicity, and pulmonary toxicity

Cardiomyopathy: Trastuzumab products can result in subclinical and clinical cardiac failure manifesting as CHF, and decreased LVEF, with greatest risk when administered concurrently with anthracyclines. Evaluate cardiac function prior to and during treatment. Discontinue KANJINTI for cardiomyopathy.

Infusion Reactions, Pulmonary Toxicity: Discontinue KANJINTI for anaphylaxis, angioedema, interstitial pneumonitis, or acute respiratory distress syndrome.

Embryo-Fetal Toxicity: Exposure to trastuzumab products during pregnancy can result in oligohydramnios, in some cases complicated by pulmonary hypoplasia and neonatal death. Advise patients of these risks and the need for effective contraception.

Read this with the rest of the clinical information

About Kanjinti

Overview

Kanjinti (trastuzumab-anns) is a monoclonal antibody medicine given into a vein. It is used in adults to treat breast cancer and metastatic stomach or gastroesophageal junction adenocarcinoma that overexpress HER2, meaning the cancer cells have high levels of this protein. Testing is used to select patients for treatment. It binds to HER2 on cancer cells, helping to slow their growth and support immune cells in attacking them.

What it treats

- HER2-overexpressing breast cancer in adults. - HER2-overexpressing metastatic adenocarcinoma of the stomach or gastroesophageal junction in adults. Treatment eligibility is based on an FDA-approved companion diagnostic test for a trastuzumab product.

Safety information

Side effects

Common side effects vary by the cancer being treated. In adjuvant breast cancer treatment, they include headache, diarrhea, nausea and chills. In metastatic breast cancer treatment, they include fever, chills, headache, infection, difficulty sleeping, cough and rash. In metastatic gastric cancer treatment, they include low white blood cell counts, diarrhea, tiredness, anemia, mouth sores, weight loss, upper respiratory tract infections, fever, low platelet counts, inflammation of moist body linings, nose and throat inflammation, and changes in taste. Serious side effects that warrant contacting a doctor include heart muscle damage and congestive heart failure, infusion reactions, lung toxicity, and worsening of chemotherapy-related low white blood cell counts. Congestive heart failure is also listed among the most common side effects in metastatic breast cancer treatment. Kanjinti can harm an unborn baby; contact your doctor if you become pregnant during treatment.

FDA boxed warning

Cardiomyopathy, infusion reactions, embryo-fetal toxicity, and pulmonary toxicity

Cardiomyopathy: Trastuzumab products can result in subclinical and clinical cardiac failure manifesting as CHF, and decreased LVEF, with greatest risk when administered concurrently with anthracyclines. Evaluate cardiac function prior to and during treatment. Discontinue KANJINTI for cardiomyopathy.

Infusion Reactions, Pulmonary Toxicity: Discontinue KANJINTI for anaphylaxis, angioedema, interstitial pneumonitis, or acute respiratory distress syndrome.

Embryo-Fetal Toxicity: Exposure to trastuzumab products during pregnancy can result in oligohydramnios, in some cases complicated by pulmonary hypoplasia and neonatal death. Advise patients of these risks and the need for effective contraception.

A boxed warning is the strongest warning the US Food and Drug Administration requires on a medicine label. Text is taken from the official label, with internal section references removed.

When to call your doctor

- Seek medical attention immediately for difficulty breathing. - Seek medical attention immediately for swelling of your face, lips, tongue or throat. - Seek medical attention immediately for fever or chills.

If symptoms are severe or getting worse quickly, seek emergency care rather than waiting.

Before taking this medicine

The label lists no contraindications for Kanjinti. Caution is needed because it may worsen chemotherapy-induced neutropenia (a low level of certain white blood cells). Pregnancy status should be checked before treatment starts in patients who could become pregnant.

Using Kanjinti

Dosing

Dosing is set by your prescriber. Each health care professional may prescribe medication differently according to a patient's medical history and condition, so follow the directions on your prescription label and speak to your doctor or pharmacist before changing anything.

Storage

Store in the original carton below 25°C, protected from light, unless the pack states refrigeration. Do not freeze. Keep all medicines out of the sight and reach of children.

Clinical information on this page is summarised from the US FDA label KANJINTI (TRASTUZUMAB-ANNS) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [AMGEN, INC] (DailyMed, retrieved 19 September 2026).

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