Patient Medication Information: uses, side effects, how to take - Gemcitabine Sun for Injection
ABOUT THIS MEDICATION
What the medication is used for:
Gemcitabine SUN for Injection is an approved chemotherapy for the treatment of:
- Non-small cell lung cancer (NSCLC), alone or in combination with another medication
- Pancreatic Cancer;
- Bladder Cancer, in combination with another medication;
- Breast Cancer, in combination with another medication.
What it does:
Gemcitabine SUN for Injection is a chemotherapy that works through disrupting the cells ability to divide or grow. Chemotherapies are active in both healthy and cancer cells. However, cancer cells are known to divide or grow at a faster rate than most healthy cells making chemotherapies such as Gemcitabine SUN for Injection effective in the treatment of various cancers. While the time it takes to see if Gemcitabine SUN for Injection shrinks your cancer varies from person to person, your doctor will ask you if you are feeling better and will perform regularly scheduled examinations and x-rays to determine if Gemcitabine SUN for Injection has been effective.
When it should not be used:
Do not take Gemcitabine SUN for Injection if you have had an allergic or sensitivity reaction to this drug or any of its ingredients (see "'What the important nonmedicinal ingredients are" section of this leaflet).
What the medicinal ingredient is:
Gemcitabine hydrochloride.
What the nonmedicinal ingredients are:
Mannitol, sodium acetate trihydrate, hydrochloric acid and/or sodium hydroxide, nitrogen.
What dosage forms it comes in:
Gemcitabine SUN for Injection is a sterile lyophilized powder and is available in 200 mg and 1g vials.
This product contains no antimicrobial preservatives. Sodium hydroxide and hydrochloric acid are used for PH adjustments.
WARNINGS AND PRECAUTIONS
Serious Warnings and Precautions
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BEFORE you receive Gemcitabine SUN for Injection talk to your doctor if;
- You have had an allergic reaction to any chemotherapy or have been treated with any chemotherapy in the past
You are pregnant, plan on becoming pregnant, or are currently breast feeding
- You have liver or kidney problems, or a bone marrow disorder
INTERACTIONS WITH THIS MEDICATION
Gemcitabine SUN for Injection is known to increase your body's sensitivity to radiation therapy.
It is very important to tell your doctor about any medications you may be taking, including over-the-counter drugs, such as Aspirin® (acetylsalicylic acid), vitamins, and other pain relievers. Be sure to check with your doctor before taking any medications on your own.
PROPER USE OF THIS MEDICATION
Usual dose:
Your doctor will develop a Gemcitabine SUN for Injection treatment plan based on your needs. You are encouraged to discuss your treatment plan with your doctor. There are many points your doctor will consider when selecting the appropriate treatment plan for you. Your doctor may recommend skipping a dose based upon your response to Gemcitabine SUN for Injection.
Overdose:
Gemcitabine SUN for Injection will be given under the supervision of a qualified physician. Any overdose should be managed by a qualified physician experienced in the use of anticancer agents.
| If you think you, or a person you are caring for, have taken too much Gemcitabine SUN for Injection, contact a healthcare professional, hospital emergency department, or regional Poison Control Centre immediately, even if there are no symptoms. |
Missed Dose:
Contact your physician immediately for further instructions.
SIDE EFFECTS AND WHAT TO DO ABOUT THEM
In clinical studies of gemcitabine for injection (gemcitabine hydrochloride), side effects were generally manageable. Side effects significant enough to cause your treatment to be stopped occurred in about 10% of all patients. Less than 1% of patients stopped therapy due to any one side effect. Most side effects were reversible and can be managed by either a delay in your treatment, a reduction of the dose of chemotherapy or both. Therefore it is important for you to know about common side effects and for you to communicate any suspected side effects to your doctor.
You should discuss possible side effects with your doctor before beginning Gemcitabine SUN for Injection therapy and at any time you think you may be experiencing a side effect. For a list of possible side effects see the "Call Your Doctor or Nurse If You Experience" section and the Serious Side Effects Table below.
In clinical studies of Gemcitabine SUN for Injection the most common reason for dosage adjustments was low blood counts. About two thirds of patients had low blood counts. In about one fourth of patients, decreases in blood counts were severe. For more information speak with your doctor and see section below titled Low Blood Counts.
Shortness of breath may develop or worsen during treatment due to disease progression or in rare cases, due to a direct effect of the drug. If this occurs, patients should inform their treating doctor immediately of the developing or worsening of shortness of breath.
Nausea and vomiting were the most common side effects in clinical studies of Gemcitabine SUN for Injection. About two thirds of patients experienced nausea and vomiting, which were usually mild to moderate. Other common side effects included fever, swelling, rash, and flu-like symptoms.
In rare cases, Gemcitabine SUN for Injection may affect your liver, especially if you have liver metastases (spreading of cancer) or a medical history of hepatitis (inflammation of the liver), alcoholism or liver cirrhosis (liver disease). Follow your doctor's instructions on having periodic blood tests to check your liver.
In rare cases, Gemcitabine SUN for Injection may affect your kidney, especially if your kidney function is not normal. Follow your doctor's instructions on having periodic blood tests to check your kidneys.
Low Blood Counts:
Chemotherapy drugs often affect the blood cells which means that temporary changes in their counts may occur. These effects may be more common in patients older than 65 and in women. Blood tests will be done before each dose of Gemcitabine SUN for Injection to monitor your blood counts.
If your doctor notices changes in your blood counts, follow his/her advice, which may include:
White Blood Count:
- if your white blood count becomes low, you may have trouble fighting infections
- stay out of crowds and away from people with colds or other illnesses
- call your doctor if you develop a temperature over 38°C
- ensure regular mouth care to reduce chance of
- infection
Red Blood Count:
- If your red blood count becomes low, you may feel tired or weak. If it becomes too low, your doctor may recommend a red blood cell transfusion
- rest as much as you need to
- try to eat a well balanced diet
Platelet Count:
- If your platelet count becomes low, your blood may not clot as fast as usual, and bleeding or bruising may occur. Sometimes, a blood transfusion is given if platelet counts drop very low
- try to avoid getting cuts, bumps, or bruises (for example avoid contact sport and use an electric razor)
- since acetylsalicylic acid can affect your platelets, you should avoid taking acetylsalicylic acid while you are receiving chemotherapy, unless your doctor advises otherwise
Call Your Doctor or Nurse If You Experience:
- any unusual bruising or bleeding
- any pain around an infusion site
- a sore mouth or throat
- prolonged or uncomfortable swelling
- severe diarrhea, meaning three or more watery bowel movements per day, lasting more than 24 hours
- severe constipation for three days that has not been relieved by laxatives
- numbness or tingling in your hands or feet
- vomiting for more than 24 hours after your treatment
- any changes in your skin, especially rash or potential allergic skin reactions
- headache with confusion, and/or seizures (fits), and/or changes in vision
- see also the Serious Side Effects Table below
| SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM | |||
|---|---|---|---|
| Symptom / effect | Talk to your healthcare professional | ||
| Only if severe | In all cases | ||
| Very Common | Diarrhea | √ | |
| Swelling | √ | ||
| Vomiting | √ | ||
| Common | Body temperature over 38°C or shaking chills | √ | |
| Fatigue | √ | ||
| Uncommon | Shortness of breath | √ | |
| Very Rare | Skin reactions including blistering | √ | |
| Headache with confusion, and/or seizures (fits), and/or changes in vision | √ | ||
This is not a complete list of side effects. For any unexpected effects while taking Gemcitabine SUN for Injection, contact your doctor or pharmacist.
HOW TO STORE IT
Handling and storage of Gemcitabine SUN for Injection is restricted to qualified healthcare professionals.
Keep out of reach of children.
Store unopened vial at 15 to 30°C.
Reconstituted solution is stable for 24 hours between 15°C and 30°C.
REPORTING SIDE EFFECTS
You can report any suspected side effects associated with the use of health products to Health Canada by:
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
If you want more information about Gemcitabine Injection:
- Talk to your healthcare professional
- Find the full product monograph that is prepared for healthcare professionals and includes this Part III: Consumer 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 sponsor’s website at https://www.taro.ca
Or by calling 1-800-268-1975
130 East Drive
Brampton, ON L6T 1C1
