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Zelboraf

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Zelboraf

PATIENT INFORMATION

ZELBORAF®
(ZEL-bor-raf)
(vemurafenib) Tablet

WHAT IS THE MOST IMPORTANT INFORMATION I SHOULD KNOW ABOUT ZELBORAF?

ZELBORAF CAN CAUSE SERIOUS SIDE EFFECTS, INCLUDING:

Risk of cancers. ZELBORAF may cause a type of skin cancer called cutaneous squamous cell carcinoma (cuSCC). New melanoma lesions have occurred in patients taking ZELBORAF. ZELBORAF may also cause another type of cancer called non-cutaneous squamous cell carcinoma (SCC). Talk with your healthcare provider about your risk for these cancers.

Check your skin and tell your healthcare provider right away about any skin changes including a:

  • new wart
  • skin sore or reddish bump that bleeds or does not heal
  • change in size or color of a mole

Your healthcare provider should check your skin before you start taking ZELBORAF, and every 2 months while taking ZELBORAF, to look for any new skin cancers. Your healthcare provider may continue to check your skin for 6 months after you stop taking ZELBORAF.

Your healthcare provider should also check for cancers that may not occur on the skin. Tell your healthcare provider about any new symptoms that have developed while taking ZELBORAF.

See “What are the possible side effects of ZELBORAF?” for more information about side effects.

WHAT IS ZELBORAF?

ZELBORAF is a prescription medicine used to treat a type of skin cancer called melanoma,

  • that has spread to other parts of the body or cannot be removed by surgery, and
  • that has a certain type of abnormal “BRAF” gene

Your healthcare provider will perform a test to make sure that ZELBORAF is right for you.

  • ZELBORAF is not used to treat melanoma with a normal BRAF gene.

It is not known if ZELBORAF is safe and effective in children under 18 years of age.

WHAT SHOULD I TELL MY HEALTHCARE PROVIDER BEFORE TAKING ZELBORAF?

Before you start taking ZELBORAF, tell your healthcare provider if you:

  • have any heart problems, including a condition called long QT syndrome
  • have liver or kidney problems
  • have been told that you have low blood levels of potassium, calcium, or magnesium
  • have any other medical conditions
  • are pregnant or plan to become pregnant. ZELBORAF may harm your unborn baby.
    • Females who are able to become pregnant, and males who take ZELBORAF, should use birth control during treatment and for 2 months after stopping ZELBORAF.
    • Talk to your healthcare provider about birth control methods that may be right for you.
    • Tell your healthcare provider right away if you become pregnant during treatment with ZELBORAF.
  • are breastfeeding or plan to breastfeed. It is not known if ZELBORAF passes into your breast milk. You and your healthcare provider should decide if you will take ZELBORAF or breastfeed. You should not do both.

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine.

HOW SHOULD I TAKE ZELBORAF?

  • Take ZELBORAF exactly as your healthcare provider tells you. Do not change your dose or stop ZELBORAF unless your healthcare provider tells you.
  • Take ZELBORAF every 12 hours with or without a meal.
  • Do not crush or chew ZELBORAF tablets.
  • Do not take an additional dose if vomiting occurs after ZELBORAF administration, but continue with your next dose as prescribed.
  • If you miss a dose, take it as soon as you remember. If it is within 4 hours of your next scheduled dose, just take your next dose at your regular time. Do not make up for the missed dose.
  • If you take too much ZELBORAF, call your healthcare provider or go the nearest hospital emergency room right away.

WHAT SHOULD I AVOID WHILE TAKING ZELBORAF?

Avoid sunlight while you are taking ZELBORAF. ZELBORAF can make your skin sensitive to sunlight. You may burn more easily and get severe sunburns. To help protect against sunburn:

  • When you go outside, wear clothes that protect your skin, including your head, face, hands, arms, and legs.
  • Use lip balm and a broad-spectrum sunscreen with SPF 30 or higher.

WHAT ARE THE POSSIBLE SIDE EFFECTS OF ZELBORAF?

ZELBORAF may cause serious side effects, including:

  • See “What is the most important information I should know about ZELBORAF?”
  • Allergic reactions can happen while taking ZELBORAF, and can be severe. Stop taking ZELBORAF and get medical help right away if you have any of these symptoms of an allergic reaction:
    • get a rash or redness all over your body
    • have throat tightness or hoarseness
    • feel faint
    • have a fast heartbeat
    • have trouble breathing or swallowing
    • have swelling of the face, lips, or tongue
  • Severe skin reactions. Stop taking ZELBORAF and call your healthcare provider right away if you get a skin rash with any of the following symptoms, because you may have a severe skin reaction:
    • blisters on your skin
    • fever
    • blisters or sores in your mouth
    • redness or swelling of your face, hands, or soles of your feet
    • peeling of your skin
  • Changes in the electrical activity of your heart called QT prolongation. QT prolongation can cause irregular heartbeats that can be life-threatening. Your healthcare provider should do tests before you start taking ZELBORAF and during treatment with ZELBORAF to check the electrical activity of your heart.

Tell your healthcare provider right away if you feel faint, lightheaded, dizzy, or feel your heart beating irregularly or fast while taking ZELBORAF. These may be symptoms related to QT prolongation.

  • Abnormal liver function tests. Your healthcare provider should do blood tests to check your liver function before you start taking ZELBORAF and during treatment. Tell your healthcare provider right away if you get any of these symptoms of a liver problem during treatment:
    • your skin or the whites of your eyes turn yellow
    • you feel tired
    • your urine turns dark or brown (tea color)
    • you have nausea or vomiting
    • you do not want to eat
    • pain on the right side of your stomach
  • Eye problems. Tell your healthcare provider right away if you get any of these symptoms during treatment with ZELBORAF:
    • eye pain, swelling, or redness
    • blurred vision or other vision changes during treatment with ZELBORAF

The most common side effects of ZELBORAF include:

  • joint pain
  • sunburn or sun sensitivity
  • rash (see “Severe skin reactions” above)
  • nausea
  • hair loss
  • itching
  • tiredness
  • warts

Tell your healthcare provider if you have any side effect that bothers you or that does not go away.

These are not all the possible side effects of ZELBORAF. For more information about side effects, ask your healthcare provider or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1800-FDA-1088.

You may also report side effects to Genentech at 1-888-835-2555.

HOW SHOULD I STORE ZELBORAF?

  • Store ZELBORAF at room temperature between 68°F to 77°F (20°C to 25°C).
  • Store ZELBORAF in the original container with the lid tightly closed.
  • Ask your healthcare provider or pharmacist how to safely throw away (dispose of) any unused or expired ZELBORAF.

Keep ZELBORAF and all medicine out of the reach of children.

GENERAL INFORMATION ABOUT ZELBORAF

Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use ZELBORAF for a condition for which it was not prescribed. Do not give ZELBORAF to other people, even if they have the same symptoms that you have. It may harm them.

If you would like more information, talk with your healthcare provider. You can ask your healthcare provider or pharmacist for information about ZELBORAF that is written for health professionals.

For more information, call Genentech at 1-888-835-2555.

WHAT ARE THE INGREDIENTS IN ZELBORAF?

Active ingredient: vemurafenib

Inactive ingredients: hypromellose acetate succinate, croscarmellose sodium, colloidal silicon dioxide, magnesium stearate, hydroxypropyl cellulose.

Coating: pinkish white: poly (vinyl alcohol), titanium dioxide, polyethylene glycol 3350, talc, and iron oxide red.

Last reviewed on RxList: 2/18/2014
This monograph has been modified to include the generic and brand name in many instances.

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Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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