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KEYTRUDA® (pembrolizumab) 100 mg/4 mL concentrate solution for infusion is a Prescription Medicine . KEYTRUDA has risks and benefits. The KEYTRUDA Consumer Medicine Information (CMI) is available at www.medsafe.govt.nz or by clicking the 'Consumer Medicine Information' button at the top of this page . IMPORTANT SAFETY INFORMATION 
    You should not be given KEYTRUDA  if you are allergic to pembrolizumab or to any of the following inactive ingredients: histidine, histidine monohydrochloride monohydrate, sucrose, polysorbate-80, water for injection. 
    Tell your doctor if you  have a disease of your immune system such as Crohn’s disease, ulcerative colitis, or lupus; have had an organ transplant or have had a bone marrow (stem cell) transplant that used donor stem cells (allogeneic); have pneumonia or swelling of your lungs (called pneumonitis); or have liver damage.
    If you are pregnant, think you may be pregnant or are planning to have a baby, tell your doctor.  KEYTRUDA can cause harm or death to your unborn baby. Effective contraception must be used during treatment with KEYTRUDA and for at least 4 months after the last dose of KEYTRUDA for woman who could become pregnant.
    If you are breastfeeding, tell your doctor. Do not breastfeed while taking KEYTRUDA. 
    Tell your doctor if you are taking any other medicines,  including medicines that can be bought without a prescription from a pharmacy, supermarket or health food shop, or other medicines that make the immune system weak. Examples of these may include steroids, such as prednisone.
What are the possible side effects of KEYTRUDA? 
    KEYTRUDA can cause your immune system to attack normal organs and tissues in any area of your body and can affect the way they work. These side effects can sometimes become life-threatening and can lead to death. These side effects may happen anytime during treatment or even after your treatment has ended. You may experience more than one side effect at the same time. Getting medical treatment right away may help keep these problems from becoming more serious.
    Call or see your doctor right away if you develop any of the following symptoms: 
    Lung problems: 
    Intestinal problems: 
    Liver problems: 
    Hormone gland problems (especially the thyroid, pituitary, adrenal glands): 
    Kidney problems: 
    Blood sugar problems: 
    Skin problems: 
    Problems in other organs: 
    Infusion (IV) reactions: 
    Rejection of a transplanted organ: 
    Graft-versus-host-disease (GVHD) in people with bone marrow (stem cell) transplant that uses donor stem cells (allogeneic): 
    Common side effects: 
    The side effects listed below are additional common side effects that may occur when KEYTRUDA is given together with another treatment, in addition to the very common side effects listed above.
    With chemotherapy or chemotherapy + radiotherapy:  hair loss, vomiting, decreased number of red blood cells, white blood cells and platelets in the blood, mouth sores, fever, decreased appetite, and swelling of the lining of the digestive system (for example mouth, intestines).
    With axitinib:  high blood pressure, decreased appetite, blisters or rash on palms of your hands and soles of your feet, increased liver enzyme levels, hoarseness, and constipation.
    With lenvatinib:  high blood pressure, decreased appetite, vomiting, weight loss, headache, constipation, hoarseness, urinary tract infection, stomach-area (abdominal pain), blisters or rash on the palms of your hands and soles of your feet, protein in your urine, increased liver enzyme levels, and feeling weak.
    In children, common side effects of KEYTRUDA include fever, vomiting, headache, stomach pain, decreased number of red blood cells, cough, and constipation.
    These are not all of the possible side effects of KEYTRUDA. If you have any side effects, talk to your doctor. 
    KEYTRUDA may be used to treat certain adults  with the following types of advanced cancers:
     melanoma     
     non-small cell lung cancer     
     urothelial carcinoma     
    classical Hodgkin Lymphoma     
     head and neck squamous cell carcinoma     
     renal cell carcinoma     
     oesophageal carcinoma     
     cervical cancer     
     endometrial carcinoma     
     gastric or gastroesophageal junction adenocarcinoma     
     triple-negative breast cancer     
     cutaneous squamous cell carcinoma     
     a kind of cancer that can occur in any part of the body and is shown by a laboratory test to be microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR)     
     colon or rectal cancer that is shown by a laboratory test to be MSI-H or dMMR     
    Merkel cell carcinoma     
    biliary tract carcinoma     
    malignant pleural mesothelioma     
 
    KEYTRUDA may also be used in certain adults: 
    after surgery to remove melanoma, non-small cell lung cancer, or renal cell carcinoma to help prevent the cancer from coming back     
    before surgery to treat triple-negative breast cancer or non-small cell lung cancer and then continued after surgery to help prevent their cancer from coming back     
     to treat bladder cancer which has not spread to nearby tissues but is at high-risk of spreading and where bladder removal is not preferred     
 
    KEYTRUDA may be used in children 
    KEYTRUDA may be given in combination with other anti-cancer treatments. It is important that you also read the Consumer Medicine Information for these other medicines. If you have any questions about these medicines, please ask your doctor.
    Based on the KEYTRUDA Consumer Medicines Information and Data Sheet dated 11th  August 2025.
    Talk to your doctor about whether KEYTRUDA is a suitable treatment option for you. 
    KEYTRUDA is funded to treat certain patients with the following cancers:  melanoma, non-small cell lung cancer, MSI-H or dMMR colorectal cancer, triple-negative breast cancer, head and neck squamous cell carcinoma, urothelial carcinoma, and cHL. Patients must meet specific criteria to qualify for funding.
    If KEYTRUDA is not funded for your particular cancer, you will need to pay the full cost of the medicine and its administration. Talk to your doctor about whether you qualify for funding, the cost of the medicine, and any other fees that may apply.
    Merck Sharp & Dohme (New Zealand) Limited, Level 3, 123 Carlton Gore Road, Newmarket, Auckland. 
    TAPS NP23464 TAPS DA 2514KN NZ-KEY-00885v16 Last updated October 2025
    Copyright © 2025 Merck & Co., Inc., Rahway, NJ, USA and its affiliates. All rights reserved.