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Topotecan for Injection (Fresenius Kabi Canada): Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx) Current status: Cancelled Post Market
Strength:
4 mg
ATC code:

Patient Medication Information: uses, side effects, how to take - Topotecan for Injection (Fresenius Kabi Canada)

ABOUT THIS MEDICATION

What the medication is used for

Topotecan for Injection (topotecan hydrochloride) is used for the treatment of:

  • ovarian cancer (metastatic) after failure of initial or subsequent therapy.
  • sensitive small cell lung cancer after failure of first line chemotherapy (defined as recurrence at least 60 days after first line chemotherapy).

What it does

Topotecan for Injection helps destroy tumours. It acts on an enzyme (topoisomerase-I) to prevent growth of tumour cells.

When it should not be used

Do not take Topotecan for Injection if:

  • you are hypersensitive (allergic) to topotecan or any of the other ingredients of Topotecan for Injection.
  • you are pregnant or breast-feeding;
  • you have severe kidney disease;
  • results of your last blood test show that you are not able to receive topotecan hydrochloride (severe bone marrow depression). Your doctor will tell you.

What the medicinal ingredient is

The medicinal ingredient is topotecan hydrochloride.

What the important nonmedicinal ingredients are

The nonmedicinal ingredients consist of mannitol, tartaric acid, hydrochloric acid and/or sodium hydroxide may be added to adjust the pH.

What dosage forms it comes in

Topotecan for Injection (topotecan hydrochloride) is supplied as sterile powder in single-dose vials. Each vial contains 4 mg of topotecan. Before infusion the powder needs to be reconstituted and diluted.

WARNINGS AND PRECAUTIONS

Serious Warnings and Precautions

Topotecan for Injection should be administered under the supervision of a physician experienced in the use of cancer chemotherapeutic agents.

Possible serious side effect includes:

  • a decrease in the number of cells produced in your bone marrow (bone marrow suppression), especially a type of white blood cells called neutrophils (neutropenia).
  • Bowel inflammation which may cause severe pain in your abdomen, with fever and a decrease in white blood cells which can potentially be fatal (neutropenic colitis).
  • Lung inflammation which may cause severe coughing, shortness of breath and fever which can potentially be fatal (interstitial lung disease).

BEFORE you use Topotecan for Injection talk to your doctor or pharmacist if:

  • you are hypersensitive (allergic) to topotecan or any of the other ingredients of Topotecan for Injection.
  • you are pregnant or breast-feeding.
  • results of your last blood test show that you are not able to receive topotecan hydrochloride, your doctor will tell you.
  • you have kidney disease.

Use of this medicine during Pregnancy and Breast Feeding

You should not be given Topotecan for Injection if you are pregnant or think you are pregnant.

Nursing Mothers

Do not breast-feed if you are receiving Topotecan for Injection. You should not restart breast-feeding until the doctor tells you it is safe.

Use in Children

Use in children is not recommended as safety and effectiveness have not been established.

Effect on ability to drive and use machinery

Topotecan for Injection may make you feel tired. Do not drive or operate any tools or machines if you feel tired or weak.

INTERACTIONS WITH THIS MEDICATION

It is important that your doctor know about all your medications so that you get the best possible treatment. Tell your doctor about all the medicines you are taking including those you have bought without a prescription.

PROPER USE OF THIS MEDICATION

Usual dose

The dose of Topotecan for Injection which you will receive will be based on your body size (surface area) and the results of blood tests carried out before treatment.

The recommended dose of Topotecan for Injection is 1.5 mg/m2 by intravenous infusion over 30 minutes daily for 5 consecutive days, starting on day one of a 21-day course. Prior to administration, Topotecan for Injection powder must be dissolved with water. The topotecan solution will be diluted further using either Sodium Chloride solution or Dextrose solution. A minimum of four courses of Topotecan for Injection is recommended.

Insufficient data are available in children to provide a dosage recommendation.

Remember: This medicine is for you. Only a doctor can prescribe it for you. Never give it to someone else. It may harm them even if their symptoms are the same as yours.

Overdose

If you think you have been given too much Topotecan for Injection, contact your healthcare professional, hospital emergency department or regional Poison Control Centre immediately, even if there are no symptoms.

Accidental overdosage may result in low blood pressure, fast heart rate and bleeding of the bowel.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

Like all medicines, Topotecan for Injection can have side effects. The most common side effects with Topotecan for Injection are:

  • a temporary reduction in the amount of new blood cells produced by your body, particularly of a type of white blood cell which is important for your body to prevent and fight-off an infection. In approximately 1 in 20 patients a serious infection is caught during treatment which can be fatal. If at any time during treatment you feel unwell or develop a temperature you should contact your doctor immediately.
  • you may become temporarily anemic and tired or take longer for a minor injury to stop bleeding. The reduction in the amount of blood cells (lasts for only a few days), starting from approximately day 8 of each treatment cycle and lasting for about a week. In most cases the level of blood cells return to normal in time for the next cycle of treatment.
  • Gastrointestinal perforations (including life-threatening and fatal cases) have been reported with topotecan-treated patients. Your doctor will monitor you for the possibility of GI perforation if you experience symptoms of severe stomach pain, nausea, vomiting and/or bloody stool and will discontinue Topotecan for Injection if you have an intestinal perforation.

Other possible side effects are:

  • nausea (feeling sick or queasy or having the urge to throw up)
  • vomiting (throwing up)

    • diarrhea (frequent and watery bowel movements)
    • fever
    • hair loss
    • stomach pain
    • constipation
    • swelling and pain of the mouth, tongue or gums
    • fatigue (tiredness)
    • weakness
    • anorexia (weight loss and loss of appetite)
    • feeling unwell
    • headache
    • coughing
    • shortness of breath
    • yellow skin (jaundice)
    • rash
    • itching sensation
    • mild pain and inflammation at the site of injection. Severe allergic reactions have been reported rarely.
    • lung inflammation (interstitial lung disease) has been reported rarely. Signs include difficulty in breathing, severe cough and fever.

Several of these effects may occur during your treatment. If you notice any of these, or any other effects not mentioned in this leaflet between courses or when you leave hospital/after treatment has finished, tell your doctor, nurse or pharmacist.

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM
FrequencySide Effect/SymptomTalk with your Doctor immediately
Very commonAny sign of fever or infection, or any unexpected bruising or bleedingX
CommonSerious infection; local symptoms such as sore throat or urinary problems (for example, a burning sensation when urinating, which may be caused by a urinary infection)X
UncommonSevere allergic reaction and symptoms such as swelling of the mouth, throat, difficulty in breathing, rash, hives, increased heart rate, and collapseX
RareSevere bleedingX

Severe abdominal pain, fever and diarrhoea (rarely with blood).

These could be signs of bowel inflammation (colitis)

X
Severe cough, shortness of breath, fever (interstitial lung disease). You are at increased risk if you have had radiation treatment to your lungs, or have previously takenX
medicines that caused lung damage.
Frequency not known (events from spontaneous reports)Severe stomach pain, nausea, vomiting of blood, black or bloody stools. (Possible symtpoms of gastrointestinal perforation).X
Mouth sores, difficulty swallowing, abdominal pain, nausea, vomiting, diarrhoea, bloody stool which could be signs and symptoms of inflammation of the inner lining of the mouth, stomach and/or gut (mucosal inflammation).X

This is not a complete list of side effects. For any unexpected effects while taking Topotecan for Injection contact your doctor or pharmacist.

HOW TO STORE IT

Unopened vials of Topotecan for Injection are stable until the date indicated on the package, when stored between 15 °C and

30 °C and protected from light in the original package.

Reconstituted Solutions

Since the vials contain no preservative, it is recommended that the product should be used immediately after reconstitution. If not used immediately, the reconstituted solution should be stored in a refrigerator between 2 °C and 8 °C or stored at room temperature between 15 ºC and 30 ºC and discarded after 24 hours.

Diluted solutions

Reconstituted vials of Topotecan for Injection diluted for infusion are stable up to 24 hours at room temperature between 15 ºC and 30 ºC with ambient lighting conditions. If not used immediately, the diluted solution should be stored in a refrigerator between 2 °C and 8 °C, up to 24 hours, and in line with good pharmaceutical practice.

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/adverse-reaction-reporting.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.

MORE INFORMATION

This document plus the full product monograph, prepared for health professionals can be obtained by visiting the Health Canada website (https://health-products.canada.ca/dpd-bdpp/index-eng.jsp); Fresenius Kabi Canada’s website (http://www.fresenius-kabi.com/en-ca/), or by calling 1-877-821-7724.

Fresenius Kabi Canada Ltd.

165 Galaxy Blvd, Suite 100

Toronto, ON M9W 0C8

Last Revised: April 17, 2019

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02346656

Revision date stated in the text: April 17, 2019

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 Topotecan for Injection (Fresenius Kabi Canada)

Rx or OTC
Prescription (Rx)?
DIN 02346656
Schedule(s) PRESCRIPTION
Active ingredient(s) Topotecan (topotecan hydrochloride) 4 MG
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. L01C Plant alkaloids and other natural products, antineoplastic drugs
        1. L01CE Topoisomerase 1 (TOP1) inhibitors
          1. L01CE01 Topotecan
Company FRESENIUS KABI CANADA LTD
Current status Cancelled Post Market
Current status date July 20, 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.