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Nat-Bendamustine: Uses, Side Effects and Dosage

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Facts
Status:
Prescription (Rx)
Strength:
25 mg, 100 mg
Active ingredient:

Patient Medication Information: uses, side effects, how to take - Nat-Bendamustine

What is NAT-BENDAMUSTINE used for?

NAT-BENDAMUSTINE is used to treat adults with:

  • Relapsed indolent B-cell non-Hodgkin lymphoma (NHL), whose disease

    • worsened after treatment with rituximab, or
    • did not respond to previous treatment with rituximab.
  • Chronic lymphocytic leukemia (CLL) that has not been previously treated.

How does NAT-BENDAMUSTINE work?

NAT-BENDAMUSTINE has been shown to cause cell death. The exact way in which NAT-BENDAMUSTINE kills cells is not completely understood.

What are the ingredients in NAT-BENDAMUSTINE?

Medicinal ingredients: Bendamustine hydrochloride

Non-medicinal ingredients: Mannitol

NAT-BENDAAMUSTINE comes in the following dosage forms:

Powder: 25 mg and 100 mg

Do not use NAT-BENDAMUSTINE if:

Serious Warnings and Precautions

NAT-BENDAMUSTINE should not be used in patients with serious infections.

Possible serious side effects with NAT-BENDAMUSTINE include:

  • serious infection, which can lead to death.
  • other types of cancers.
  • decreased production of blood cells. This is called myelosuppression. It may make you feel tired or bleed more easily. It may also you more likely to get an infection.
  • serious heart problems, which can lead to death.
  • serious skin reactions that can lead to death.
  • if you are allergic to bendamustine hydrochloride or to any of the other ingredients in NAT-BENDAMUSTINE including mannitol.

To help avoid side effects and ensure proper use, talk to your healthcare professional before you take NAT-BENDAMUSTINE. Talk about any health conditions or problems you may have, including if you:

  • have any heart problems or high blood pressure
  • have any infection including HIV or hepatitis B virus (HBV)
  • have kidney or liver problems
  • are planning to have a vaccine
  • are under 18 years of age. NAT-BENDAMUSTINE has not been shown to be effective in these patients.

Other warnings you should know about:

NAT-BENDAMUSTINE may also cause:

  • Extravasation. This happens when the drug leaks from the vein into the surrounding tissue. Your healthcare professional will monitor your infusion site for signs of extravasation after you have been given NAT-BENDAMUSTINE.
  • Tumor lysis syndrome (TLS). This is caused by the sudden, rapid death of cancer cells. You may be recommended to drink more fluids during your treatment and may need to have blood tests done.
  • Liver problems, which can include the reactivation of a previous HBV infection.
  • Infusion reactions and anaphylaxis. If you experience swelling of the face, lips or tongue, difficulty breathing, rash, or fainting, you may be having a reaction. If this happens, you may need to take other medications before your next NAT-BENDAMUSTINE treatment. If the reaction is severe, your treatment may be discontinued.
  • Other cancers including non-melanoma skin cancer.
  • Changes in the rhythm of the heart. This is called QTc prolongation.
  • Progressive multifocal leukoencephalopathy. This is a brain infection.

See the Serious Side Effects and What to do About them Table below, for information on these and other serious side effects.

Pregnancy and breastfeeding information for women:

  • If you are pregnant or are planning to get pregnant, there are specific risks you should discuss with your healthcare professional.
  • Taking NAT-BENDAMUSTINE during pregnancy is not recommended. It can harm an unborn baby.
  • Avoid becoming pregnant while you are using NAT-BENDAMUSTINE. You should use an effective type of birth control before and during your treatment. Start using this birth control 2 weeks before receiving NAT-BENDAMUSTINE. Continue using it until at least 4 weeks after your last dose.
  • If you become pregnant or think you are pregnant during your treatment, tell your healthcare professional right away.
  • It is not known if NAT-BENDAMUSTINE passes into breastmilk. If you are breastfeeding or planning to breastfeed, you and your healthcare professional will talk about whether you should use NAT-BENDAMUSTINE or breastfeed. You should not do both.

Fertility and pregnancy information for men:

  • NAT-BENDAMUSTINE may affect your ability to father a child.
  • Avoid fathering a child while you are using NAT-BENDAMUSTINE. You should use an effective type of birth control before and during your treatment. Start using this birth control 2 weeks before your first treatment and continue until at least 4 weeks after your last dose.
  • If your sexual partner becomes pregnant, or thinks she is pregnant, during your treatment, contact your healthcare professional right away.

Tests and check-ups:

  • You will need to have blood tests before and during your treatment. The results of these blood tests will help to tell your healthcare professional if you are experiencing some side effects. They will also show how NAT-BENDAMUSTINE is affecting your blood, liver, kidneys and heart.
  • If you have a history of heart problems, you may also need to have electrocardiograms during your treatment.
  • Your healthcare professional will check your skin during your treatment.

Tell your healthcare professional about all the medicines you take, including any drugs, vitamins, minerals, natural supplements or alternative medicines.

The following may interact with NAT-BENDAMUSTINE:

It is not known whether NAT-BENDAMUSTINE interacts with other drugs as this has not been tested; however, the following may interact with NAT-BENDAMUSTINE:

  • A medicine used to treat bacterial infections called ciprofloxacin;
  • A medicine used to treat depression called fluvoxamine;
  • A medicine used to treat heartburn called omeprazole; and
  • Smoking.

How to take NAT-BENDAMUSTINE:

NAT-BENDAMUSTINE will be given to you by a healthcare professional. The NAT-BENDAMUSTINE powder is first mixed into a solution. This solution is then given to you through a vein in your arm. This is called an intravenous (IV) infusion.

Usual dose: The dose you will receive will depend on your disease and will be measured based on your height and weight.

Relapsed indolent non-Hodgkin lymphoma: 120 mg/m2 by IV infusion over 60 minutes. NAT-BENDAMUSTINE is given on days 1 and 2 of each 21-day cycle. For this condition, you will receive NAT-BENDAMUSTINE for up to 8 cycles.

Chronic lymphocytic leukemia (CLL): 100 mg/m2 given by IV infusion over 30 minutes. NAT-BENDAMUSTINE is given on days 1 and 2 of each 28-day cycle. For this condition, you will receive NAT-BENDAMUSTINE for up to 6 cycles.

Your healthcare professional may lower your dose of NAT-BENDAMUSTINE or stop your treatment for a short time. This can happen if you experience side effects. If you have CLL, your healthcare professional may also decide to increase your dose of NAT-BENDAMUSTINE.

Overdose:

If you think you, or a person you are caring for, have taken too much NAT-BENDAMUSTINE, contact a healthcare professional, hospital emergency department, or regional poison control centre immediately, even if there are no symptoms.

Missed Dose:

NAT-BENDAMUSTINE should be given on a fixed schedule. If you miss an appointment, call your doctor for instructions.

What are possible side effects from using NAT-BENDAMUSTINE?

These are not all the possible side effects you may have when taking NAT-BENDAMUSTINE. If you experience any side effects not listed here, tell your healthcare professional.

  • fatigue
  • constipation

NAT-BENDAMUSTINE can cause abnormal blood test results. Your healthcare professional will decide when to perform blood tests and will interpret the results.

Serious side effects and what to do about them
Symptom / effectTalk to your healthcare professionalStop taking drug and get immediate medical help
Only if severeIn all cases
COMMON
Dehydration (when body does not have enough fluids): feeling thirsty, dry mouth, headache, dark yellow urine√
Hypertension (high blood pressure): severe headache, fatigue or confusion√
Hyperuricemia (high blood level of uric acid): Severe pain in your joints or redness and swelling in your joints√
Hypokalemia (low blood level of potassium): muscle twitches, cramps or weakness or muscles that will not move√
Infections: fever, chills, nausea, vomiting, diarrhea, generally feeling unwell√
Nausea and vomiting√
Serious side effects and what to do about them
Symptom / effectTalk to your healthcare professionalStop taking drug and get immediate medical help
Only if severeIn all cases
New fever or temperature higher than 38°C√
Severe or worsening rash or itching√√
Myelosuppression (low blood cell counts): Shortness of breath, significant fatigue, bleeding, fever or other signs of infection√
Pulmonary fibrosis (scarring of the lung): difficulty breathing, cough, fatigue√
Pneumonia (infection in the lungs): cough, shortness of breath√
Kidney failure (severe kidney problems): confusion; itchiness or rashes; puffiness in your face and hands; swelling in your feet or ankles; urinating less or not at all; weight gain√
Cancer (development of abnormal cells that divide uncontrollably). Symptoms may include but are not limited to: weight loss, fatigue, night sweats, loss of appetite, coughing up blood or a cough that does not go away, fever, frequent or severe infections, bone pain√
UNCOMMON
Allergic reaction including serious reactions (anaphylaxis) and infusion reactions: Skin reactions such as rash or itching, facial swelling, or difficulty breathing during or soon after infusion√√
QTc Prolongation (a heart rhythm condition): irregular heartbeat, fainting, loss of consciousness, seizure√
Tumor Lysis Syndrome (the sudden, rapid death of cancer cells): Lack of urination, severe muscle weakness, heart rhythm disturbances and seizures√√
Serious side effects and what to do about them
Symptom / effectTalk to your healthcare professionalStop taking drug and get immediate medical help
Only if severeIn all cases
Diarrhea√
RARE
Extravasation (leakage of drug from the vein after administration): redness, swelling, pain, infection at the site of infusion√

Severe skin reactions (including Stevens-Johnson Syndrome, Toxic epidermal necrolysis and drug reaction with eosinophilia):

Severe or worsening itching, intense redness, formation of hives, blisters or ulcers associated with either fever, joint pain, or a general unwell feeling. Can lead to death.

√√

Heart Failure:

Chest pain, dizziness, fatigue, rapid breathing, shortness of breath, swelling of the feet or legs.

√√
Myocardial infarction (heart attack): Pressure or squeezing pain between the shoulder blades, in the chest, jaw, left arm or upper abdomen, shortness of breath, dizziness, fatigue, lightheadedness, clammy skin, sweating, indigestion, anxiety.√√

Liver Injury:

Pain in the right abdomen, fever, fatigue, weakness, loss of appetite, jaundice, yellow color in the eyes, dark urine.

√√
VERY RARE
Progressive multifocal leukoencephalopathy (a rare brain infection): memory loss, trouble thinking, difficulty walking or sight loss.√√
Non-melanoma skin cancer: lumps or discoloured patches on the skin√
Serious side effects and what to do about them
Symptom / effectTalk to your healthcare professionalStop taking drug and get immediate medical help
Only if severeIn all cases

Nephrogenic diabetes insipidus (disorder of water balance): Extreme thirst, frequent urination of pale urine, frequent

urination during the night

√

If you have a troublesome symptom or side effect that is not listed here or becomes bad enough to interfere with your daily activities, tell your healthcare professional.

Reporting Side Effects

You can report any suspected side effects associated with the use of health products to Health Canada by:

  • Visiting the Web page on Adverse Reaction Reporting (https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada.html) for information on how to report online, by mail or by fax; or
  • Calling toll-free at 1-866-234-2345.

NOTE: Contact your health professional if you need information about how to manage your side effects. The Canada Vigilance Program does not provide medical advice.

Storage:

Your healthcare professional will store NAT-BENDAMUSTINE at 15-30°C. It will be kept in the original package until time of use to protect it from light.

Your healthcare professional will keep NAT-BENDAMUSTINE out of reach and sight of children.

If you want more information about NAT-BENDAMUSTINE:

  • Talk to your healthcare professional
  • Find the full product monograph that is prepared for healthcare professionals and includes this Patient Medication Information by visiting the Health Canada website: (https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/drug-product-database.html); the manufacturer’s website www.natcopharma.ca or by calling 1-800-296-9329.

Last Revised: MAY 05, 2023

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02496887

Revision date stated in the text: May 5, 2023

Found a mistake? Write to us via the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Nat-Bendamustine

Rx or OTC
Prescription (Rx)?
DIN 02496887, 02496895
Schedule(s) PRESCRIPTION
Active ingredient(s) Bendamustine hydrochloride
Dosage form(s) Powder For Solution
Route(s) of administration Intravenous
Drug class (WHO ATC)
  1. L Antineoplastic and immunomodulating agents
    1. L01 Antineoplastic agents
      1. L01A Alkylating agents
        1. L01AA Nitrogen mustard analogues
          1. L01AA09 Bendamustine
Company NATCO PHARMA (CANADA) INC
Current status Marketed
Current status date February 25, 2021
Strengths and forms
DIN Strength Dosage form(s) Current status
02496887 25 MG Powder For Solution Marketed February 25, 2021
02496895 100 MG Powder For Solution Marketed February 25, 2021

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.