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SAVINGS AND SUPPORT

FOR TRUXIMA

Actor portrayal.

THE Teva CORE PROGRAM

Teva offers a range of services through the Comprehensive Oncology Reimbursement Expertise (CORE) program.

Teva offers a range of services through the Comprehensive Oncology Reimbursement Expertise (CORE) program.

  • Benefits verification and coverage determination
  • Support for precertification and prior authorization
  • Teva Cares Foundation patient assistance program referrals

Up to $25,000 per year

*The cost support program for TRUXIMA helps commercially insured individuals.

The TRUXIMA Cost Support Program helps commercially insured patients in the United States (including the United States territories) who are prescribed TRUXIMA (rituximab-abbs) for covered indications pay for their eligible out-of-pocket costs for the drug. The Program does not cover the costs of physician office visits or evaluations, blood work or other testing, or transportation. See complete Terms and Conditions at TRUXIMASavingsOffer.com. Eligible Patients must have commercial insurance coverage for TRUXIMA. Uninsured and cash-paying patients are NOT eligible for this Program. Patients enrolled in any state or federally funded healthcare program are NOT eligible for this Program, nor are patients with commercial insurance coverage that does not provide coverage for TRUXIMA. Call for more information: 1-888-587-3263.

See full Terms and Conditions for eligibility and restrictions.

Helping patients is at the CORE of what we do

 

 

 

 

See if you are eligible to save on TRUXIMA, and get insurance and reimbursement information.

To learn more

VISIT TevaCORE.com

CALL

1-888-587-3263

Monday–Friday, 9 AM–6 PM (EST)

Downloadable materials and links to resources

Questions for your doctor

Get the discussion with your doctor going with these helpful questions about CLL, NHL, and treatment with TRUXIMA

 

 

 

 

Download questions

PATIENT BROCHURE FOR TRUXIMA

Check out this comprehensive resource about TRUXIMA

 

 

 

 

Download BROCHURE

support and information are available from these national and non-profit organizations

Lymphoma/leukemia Organizations

The Leukemia & Lymphoma Society

1-800-955-4572

www.lls.org

Lymphoma Research Foundation

1-800-500-9976

www.lymphoma.org

Support Organizations

Patient Advocate Foundation

1-800-532-5274

www.patientadvocate.org

This is a list of sources that you may find helpful. Please note that this information was accurate at the time of publication, but is subject to change without notice. Ask your healthcare team to recommend additional resources.

APPROVED USE

TRUXIMA is a prescription medicine used to treat adults with:

  • Non-Hodgkin's Lymphoma (NHL) alone or with other chemotherapy medicines
  • Chronic Lymphocytic Leukemia (CLL): with the chemotherapy medicines fludarabine and cyclophosphamide

It is not known if TRUXIMA is safe and effective in children.

IMPORTANT SAFETY INFORMATION

TRUXIMA can cause serious side effects that can lead to death, including:

  • Infusion-related reactions. Infusion-related reactions are very common side effects of TRUXIMA treatment. Serious infusion-related reactions can happen during your infusion or within 24 hours after your infusion of TRUXIMA. Your healthcare provider should give you medicines before your infusion of TRUXIMA to decrease your chance of having a severe infusion-related reaction.

    Tell your healthcare provider or get medical help right away if you get any of these symptoms during or after an infusion of TRUXIMA:

    • hives (red itchy welts) or rash
    • shortness of breath, difficulty breathing, or wheezing
    • itching
    • weakness
    • swelling of your lips, tongue, throat, or face
    • dizziness or feel faint
    • sudden cough
    • palpitations (feel like your heart is racing or fluttering)
    • chest pain
  • Severe skin and mouth reactions. Tell your healthcare provider or get medical help right away if you get any of these symptoms at any time during your treatment with TRUXIMA:
    • painful sores or ulcers on your skin, lips, or in your mouth
    • blisters
    • peeling skin
    • rash
    • pustules
  • Hepatitis B virus (HBV) reactivation. Before you receive your TRUXIMA treatment, your healthcare provider will do blood tests to check for HBV infection. If you have had hepatitis B or are a carrier of hepatitis B virus, receiving TRUXIMA could cause the virus to become an active infection again. Hepatitis B reactivation may cause serious liver problems including liver failure and death. You should not receive TRUXIMA if you have active hepatitis B liver disease. Your healthcare provider will monitor you for hepatitis B infection during and for several months after you stop receiving TRUXIMA.

    Tell your healthcare provider right away if you get worsening tiredness, or yellowing of your skin or white part of your eyes, during treatment with TRUXIMA.

  • Progressive Multifocal Leukoencephalopathy (PML). PML is a rare, serious brain infection caused by a virus that can happen in people who receive TRUXIMA. People with weakened immune systems can get PML. PML can result in death or severe disability. There is no known treatment, prevention, or cure for PML.

    Tell your healthcare provider right away if you have any new or worsening symptoms or if anyone close to you notices these symptoms:

    • confusion
    • decreased strength or weakness on one side of your body
    • dizziness or loss of balance
    • vision problems
    • difficulty walking or talking

Before you receive TRUXIMA, tell your healthcare provider about all of your medical conditions, including if you:

  • have had a severe reaction to TRUXIMA or a rituximab product
  • have a history of heart problems, irregular heart beat, or chest pain
  • have lung or kidney problems
  • have an infection or weakened immune system
  • have or have had any severe infections including:
    • Hepatitis B virus (HBV)
    • Parvovirus B19
    • Hepatitis C virus (HCV)
    • Varicella zoster virus (chickenpox or shingles)
    • Cytomegalovirus (CMV)
    • West Nile virus
    • Herpes simplex virus (HSV)
  • have had a recent vaccination or are scheduled to receive vaccinations. You should not receive certain vaccines before or during treatment with TRUXIMA
  • are pregnant or plan to become pregnant. Talk to your healthcare provider about the risks to your unborn baby if you receive TRUXIMA during pregnancy

    Females who are able to become pregnant should use effective birth control (contraception) during treatment with TRUXIMA and for 12 months after the last dose of TRUXIMA. Talk to your healthcare provider about effective birth control.

    Tell your healthcare provider right away if you become pregnant or think that you are pregnant during treatment with TRUXIMA.

  • are breastfeeding or plan to breastfeed. It is not known if TRUXIMA passes into your breast milk. Do not breastfeed during treatment and for at least 6 months after your last dose of TRUXIMA

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Especially tell your doctor if you take or have taken:

  • a Tumor Necrosis Factor (TNF) inhibitor medicine
  • a Disease Modifying Anti-Rheumatic Drug (DMARD)

If you are not sure if your medicine is one listed above, ask your healthcare provider.

TRUXIMA can cause serious side effects, including

  • Tumor Lysis Syndrome (TLS). TLS is caused by the fast breakdown of cancer cells. TLS can cause you to have:
    • kidney failure and the need for dialysis treatment
    • abnormal heart rhythm

    TLS can happen within 12 to 24 hours after an infusion of TRUXIMA. Your healthcare provider may do blood tests to check you for TLS. Your healthcare provider may give you medicine to help prevent TLS.

    Tell your healthcare provider right away if you have any of the following signs or symptoms of TLS:

    • nausea
    • diarrhea
    • vomiting
    • lack of energy
  • Serious infections. Serious infections can happen during and after treatment with TRUXIMA, and can lead to death. TRUXIMA can increase your risk of getting infections and can lower the ability of your immune system to fight infections. Types of serious infections that can happen with TRUXIMA include bacterial, fungal, and viral infections. After receiving TRUXIMA, some people have developed low levels of certain antibodies in their blood for a long period of time (longer than 11 months). Some of these people with low antibody levels developed infections. People with serious infections should not receive TRUXIMA. Tell your healthcare provider right away if you have any symptoms of infection:
    • fever
    • cold symptoms, such as runny nose or sore throat that do not go away
    • flu symptoms, such as cough, tiredness, and body aches
    • earache or headache
    • pain during urination
    • cold sores in the mouth or throat
    • cuts, scrapes, or incisions that are red, warm, swollen, or painful
  • Heart problems. TRUXIMA may cause chest pain, irregular heartbeats, and heart attack. Your healthcare provider may monitor your heart during and after treatment with TRUXIMA if you have symptoms of heart problems or have a history of heart problems. Tell your healthcare provider right away if you have chest pain or irregular heartbeats during treatment with TRUXIMA
  • Kidney problems. TRUXIMA can cause severe kidney problems that lead to death. Your healthcare provider should do blood tests to check how well your kidneys are working
  • Stomach and serious bowel problems that can sometimes lead to death. Bowel problems, including blockage or tears in the bowel, can happen if you receive TRUXIMA with chemotherapy medicines. Tell your healthcare provider right away if you have any severe stomach-area (abdomen) pain or repeated vomiting during treatment with TRUXIMA

Your healthcare provider will stop treatment with TRUXIMA if you have severe, serious, or life-threatening side effects.

The most common side effects of TRUXIMA include:

    • infusion-related reactions
    • infections (may include fever, chills)
    • body aches
    • tiredness
    • nausea

Other side effects with TRUXIMA include:

    • aching joints during or within hours of receiving an infusion
    • more frequent upper respiratory tract infection

These are not all of the possible side effects with TRUXIMA.

Please see additional Important Safety Information throughout and full Prescribing Information, including BOXED WARNINGS and Medication Guide, to discuss with your doctor.

Call your doctor for medical advice about side effects.

You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects to Teva at 1-888-483-8279.

This information does not take the place of talking with your doctor for medical advice about your condition or treatment.

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