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Package leaflet: Information for the user

Gemcitabine 38 mg/ml Concentrate for Solution for Infusion

Gemcitabine

Read all of this leaflet carefully, before you start receiving this medicine because it contains important information for you.

•    Keep this leaflet. You may need to read it again.

• If you have further questions, please ask your doctor, nurse or pharmacist.

• If you get any side effects, talk to your doctor, or pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

What is in this leaflet:

1.    What Gemcitabine Concentrate for Solution for Infusion is and what it is used for

2.    What you need to know before you are given Gemcitabine Concentrate for Solution for Infusion

3.    How Gemcitabine Concentrate for Solution for Infusion is given

4.    Possible side effects

5.    How to store Gemcitabine Concentrate for Solution for Infusion

6.    Contents of the pack and other information

1. What Gemcitabine Concentrate for Solution for Infusion is and what it is used for

Gemcitabine Concentrate for Solution for Infusion (Gemcitabine) belongs to a group of medicines called 'cytotoxics'. These medicines kill dividing cells, including cancer cells.

Gemcitabine may be given on its own or in combination with other anti-cancer medicines (e.g. cisplatin, paclitaxel, carboplatin), depending on the type of cancer you have.

Gemcitabine is used in the treatment of the following types of cancer:

•    Non-small cell lung cancer (NSCLC), when given alone or together with cisplatin

•    Pancreatic cancer

•    Breast cancer, when given together with paclitaxel

•    Ovarian cancer, when given together with carboplatin

•    Bladder cancer, when given together with cisplatin

2. What you need to know before you are given Gemcitabine Concentrate for Solution for Infusion

You should not be given Gemcitabine if:

•    you are allergic to gemcitabine or any of the other ingredients of this medicine (listed in section 6).

•    you are breast-feeding

Warnings and precautions

Before your first infusion, you will have samples of your blood taken to check how well your kidneys and liver are working. Before each infusion, you will also have blood tests to check if you have enough blood cells to receive Gemcitabine.

Your doctor may decide to change your dose or delay treating you, based on your general health or if your blood cell counts are too low.

Periodically, you will have samples of your blood taken to evaluate your kidney and liver function.

Talk to your doctor or nurse before using Gemcitabine if:

•    you have, or have previously had liver disease, heart disease, or vascular disease

•    you have recently had, or are going to have radiotherapy

•    you have recently been vaccinated

•    you develop breathing difficulties, or feel very weak and look very pale (this may be a sign of kidney failure).

Children and adolescents

This medicine is not recommended for use in children under 18 years of age due to insufficient data on safety and efficacy.

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The following information is intended for medical or healthcare professionals only:

Gemcitabine 38 mg/ml Concentrate for Solution for Infusion

Instructions for use, handling and disposal

Use

•    Refer to the SPC to calculate the dose and the number of vials required.

•    Dilution of the solution is required: An approved diluent for Gemcitabine Concentrate for Solution for Infusion is sodium chloride 9 mg/ml (0.9%) solution for injection (without preservative). Use the aseptic technique during any further dilution of the Gemcitabine concentrate, prior to administration.

•    Parenteral products should be visually inspected for particulate matter and discolouration prior to administration. If particulate matter is observed, do not administer.

•    After dilution, chemical and physical in-use stability has been demonstrated for:

Component Specification

Item number:		Q77950
Request number:		AS4501
Country:		United Kingdom / Ireland / Malta
OI template:		88S120
Amalia version:		5
Mulgrave version:		4
Dimensions:	300 x 378 mm
Container(s):	Glass Vial
Supplier:	Howden Printing
Stock:	Primapharm 40gsm / Teropaque Thin Medical 40gsm
Folded dimensions:	31.5 x 150 mm
Printed both sides:	Yes
Perforated:	No
Pharma code:		71 (112111)
Pharma code length		9 mm
Mulgrave 4 series no.:		434471
Colours
Black:		■

b

Hospira

Tell your doctor, nurse or pharmacist if you are taking, have recently taken or might take any other medicines, including vaccinations.

Pregnancy, breast-feeding and fertility

Pregnancy

If you are pregnant, or thinking about becoming pregnant, tell your doctor. The use of gemcitabine should be avoided during pregnancy. Your doctor will discuss with you the potential risk of taking gemcitabine during pregnancy.

Breast-feeding

If you are breast-feeding, tell your doctor.

You must discontinue breast-feeding during gemcitabine treatment.

Fertility

Men are advised not to father a child during and up to 6 months following treatment with gemcitabine. If you would like to father a child during the treatment or in the 6 months following treatment, seek advice from your doctor or pharmacist. You may want to seek counselling on sperm storage before starting your therapy.

Driving and using machines

Gemcitabine may make you feel sleepy, particularly if you have consumed any alcohol. Do not drive a car or operate machinery until you are sure that Gemcitabine treatment has not made you feel sleepy.

Gemcitabine Concentrate for Solution for Infusion contains sodium

Gemcitabine Concentrate for Solution for Infusion contains up to 2.4 mg sodium (< 1 mmol) in each 200 mg vial, up to 12.1 mg sodium (< 1 mmol) in each 1 g vial and up to 24.2 mg sodium in each 2 g vial. To be taken into consideration by patients on a sodium controlled diet.

3. How Gemcitabine Concentrate for Solution for Infusion is given

Your initial dose of Gemcitabine will be calculated by your doctor and will depend on the type of cancer you have and the surface area of your body in square meters (m²).

Your height and weight are measured to work out the surface area of your body. Your doctor will use this information to work out the right dose for you. The usual dose of Gemcitabine is between 1 g/m² and 1.25 g/m².

This dosage may be adjusted, or treatment may be delayed depending on your blood cell counts, your general health and any side effects you experience.

How frequently you receive your gemcitabine infusion will depend on what type of cancer you are being treated for.

You will always receive Gemcitabine as an infusion (a slow injection via a drip) into one of your veins. The infusion will last approximately 30 minutes.

As Gemcitabine will be given to you under the supervision of a doctor, it is unlikely that you will receive the wrong dose. However, if you have any concerns about the dose you receive or if you have any further questions about the use of this medicine, please talk to your doctor, nurse or pharmacist.

4. Possible side effects

Like all medicines, gemcitabine can cause side effects, although not everybody gets them.

You must contact your doctor immediately if you notice any of the following:

•    Bleeding from the gums, nose or mouth or any bleeding that would not stop, reddish or pinkish urine, unexpected bruising (since you might have less platelets than normal which is very common).

•    Tiredness, feeling faint, becoming easily breathless or if you look pale (since you might have less haemoglobin than normal which is very common).

•    Mild to moderate skin rash (very common) /itching (common), or fever (very common); (allergic reactions).

•    Temperature of 38°C or greater, sweating or other signs of infection (since you might have less white blood cells than normal accompanied by fever also known as febrile neutropenia) (common).

•    Pain, redness, swelling or sores in your mouth (stomatitis) (common).

•    Irregular heart rate (arrhythmia) (uncommon).

•    Extreme tiredness and weakness, purpura or small areas of bleeding in the skin (bruises), acute renal failure (low urine output/or no urine output), and signs of infection (haemolytic uraemic syndrome). It may be fatal (uncommon).

•    Difficulty breathing (it is common to have mild breathing difficulty soon after the Gemcitabine infusion which soon passes, however uncommonly or rarely there can be more severe lung problems).

•    Severe chest pain (myocardial infarction) (rare).

Requester
I have checked this artwork against the registered text including spelling, layout, size, colours, registration numbers and scientific
equations, the name and address and
trademarks. Also for any possible changes to
related items.
This artwork is in conformance with the Marketing Authorisation and can now proceed
to the printing stage.
Previous Item Number: Q77025 / 434347
Signed:
Date:
Version 1		Version 2
Technician:	BE	Technician:	BE
Date:	21/Jul/14	Date:	21/Jul/14
Version 3		Version 4
Technician:	LB	Technician:	LB
Date:	25/Jul/14	Date:	23/Oct/14
Version 5		Version 6
Technician:	LB	Technician:	EM
Date:	23/Oct/14	Date:	23/Oct/14
Version 7		Version 8
Technician:	JH	Technician:	JH
Date:	24/Oct/14	Date:	08/Jan/16
Version 9		Version 10
Technician:	JH	Technician:	XX
Date:	11/Feb/16	Date:	dd/mmm/yy

•    Severe hypersensitivity/allergic reaction with severe skin rash including red itchy skin, swelling of the hands, feet, ankles, face, lips, mouth or throat (which may cause difficulty in swallowing or breathing), wheezing, fast beating heart and you may feel you are going to faint (anaphylactic reaction) (very rare).

•    Generalised swelling, shortness of breath or weight gain, as you might have fluid leakage from small blood vessels into the tissues (capillary leak syndrome) (very rare).

•    Headache with changes in vision, confusion, seizures or fits (posterior reversible encephalopathy syndrome) (very rare).

•    Severe rash with itching, blistering or peeling of the skin (Stevens-Johnson syndrome, toxic epidermal necrolysis) (very rare).

Other side effects with Gemcitabine may include:

Very common side effects (may affect more than 1 in 10 people)

•    Low white blood cells

•    Difficulty breathing

•    Vomiting

•    Nausea

•    Hair loss

•    Liver problems: found through abnormal blood test results

•    Blood in urine

•    Abnormal urine tests: protein in urine

•    Flu like symptoms including fever

•    Swelling of ankles, fingers, feet, face (oedema)

Common side effects (may affect up to 1 in 10 people)

•    Poor appetite (anorexia)

•    Headache

•    Insomnia

•    Sleepiness

•    Cough

•    Runny nose

•    Constipation

•    Diarrhoea

•    Itching

•    Sweating

•    Muscle pain

•    Back pain

•    Fever

•    Weakness

•    Chills

Uncommon side effects (may affect up to 1 in 100 people)

•    Scarring of the air sacs of the lung (interstitial pneumonitis)

•    Wheeze (spasm of the airways)

•    Scarring of the lungs (abnormal chest X ray/scan)

•    Heart failure

•    Kidney failure

•    Serious liver damage, including liver failure

•    Stroke

Rare side effects (may affect up to 1 in 1,000 people)

•    Low blood pressure

•    Skin scaling, ulceration or blister formation

•    Sloughing of the skin and severe skin blistering

•    Injection site reactions

•    Severe lung inflammation causing respiratory failure (adult respiratory distress syndrome)

•    A skin rash like severe sunburn which can occur on skin that has previously been exposed to radiotherapy (radiation recall).

•    Fluid in the lungs

•    Scarring of the air sacs of the lung associated with radiation therapy (radiation toxicity)

•    Gangrene of fingers or toes

•    Inflammation of the blood vessels (peripheral vasculitis)

Very rare side effects (may affect up to 1 in 10,000 people)

•    Increased platelet count

•    Inflammation of the lining of the large bowel, caused by reduced blood supply (ischaemic colitis)

• Low haemoglobin level (anaemia), low white blood cells and low platelet count will be detected by a blood test.

You might have any of these symptoms and/or conditions. You must tell your doctor as soon as possible when you start experiencing any of these side effects.

If you are concerned about any side effects, talk to your doctor.

Reporting of side effects

If you get any side effects, talk to your doctor or nurse. This includes any possible side effects not mentioned in this leaflet. You can also report side effects directly via

Ireland

HPRA Pharmacovigilance Earlsfort Terrace IRL - Dublin 2 Tel: +353 1 6764971 Fax: +353 1 6762517 Website: www.hpra.ie e-mail: medsafety@hpra.ie

Malta

ADR Reporting The Medicines Authority Post-Licensing Directorate 203 Level 3, Rue D'Argens GZR-1368 Gzira

Website: www.medicinesauthority.gov.mt e-mail: postlicensing.medicinesauthority@gov.mt

United Kingdom

Yellow Card Scheme

Website: www.mhra.gov.uk/yellowcard

By reporting side effects you can help provide more information on the safety of this medicine.

5. How to store Gemcitabine Concentrate for Solution for Infusion

Gemcitabine will be stored and administered by healthcare professionals, who will follow this guidance:

•    Keep this medicine out of the sight and reach of children.

•    Do not use this medicine after the expiry date which is stated on the vial and carton after EXP. The expiry date refers to the last day of that month.

•    Store in a refrigerator (2°C-8°C).

•    This medicine is for single use only; any unused solution should be discarded according to local procedures.

6. Contents of the pack and other information

What Gemcitabine Concentrate for Solution for Infusion contains

•    The active ingredient in Gemcitabine Concentrate for Solution for Infusion is gemcitabine (in the form of gemcitabine hydrochloride). The concentrated solution has a strength of 38 mg/ml, which means that every millilitre of the concentrate contains 38 milligrams of gemcitabine (in the form of gemcitabine hydrochloride).

•    The other ingredients in this medicine are Water for Injections, hydrochloric acid (for pH adjustment) and sodium hydroxide (for pH adjustment).

What Gemcitabine Concentrate for Solution for Infusion looks like and contents of the pack

•    Gemcitabine Concentrate for Solution for Infusion is a clear, colourless or light straw-coloured solution

•    Gemcitabine Concentrate for Solution for Infusion is packaged in glass vials

•    Three sizes of glass vial are available, containing either

•    200 mg gemcitabine (as hydrochloride) in 5.3 ml solution

• 1 g gemcitabine (as hydrochloride) in 26.3 ml solution

• 2 g gemcitabine (as hydrochloride) in 52.6 ml solution

•    Each vial is packed into a single outer carton

Marketing Authorisation Holder and Manufacturer

The marketing authorisation holder is Hospira UK Limited, Horizon, Honey Lane, Hurley, Maidenhead, SL6 6RJ UK.

The manufacturer is Hospira UK Limited, Horizon, Honey Lane, Hurley, Maidenhead,

SL6 6RJ UK.

This leaflet was last revised in 03/2016.

X-------------------------------------------------------

From a microbiological point of view, the product should be used immediately. If not used immediately, in-use storage times and conditions prior to use are the responsibility of the user and would normally not be longer than 24 hours at 2 to 8°C, unless dilution has taken place in controlled and validated aseptic conditions.

Handling

•    The normal safety precautions for cytostatic agents must be observed when preparing and disposing of the infusion solution. Handling of the concentrate should be done in a safety box and protective coats and gloves should be used. If no safety box is available, the equipment should be supplemented with a mask and protective glasses.

•    If the preparation comes into contact with the eyes, this may cause serious irritation. The eyes should be rinsed immediately and thoroughly with water. If there is lasting irritation, a doctor should be consulted. If the solution is spilled on the skin, rinse thoroughly with water.

Disposal

•    Gemcitabine Concentrate for Solution for Infusion is for single use only. Any unused product or waste material should be disposed of in accordance with local requirements.

Q77950

434471

Component Specification

Item number:		Q77950
Request number:		AS4501
Country:		United Kingdom / Ireland / Malta
OI template:		88S120
Amalia version:		5
Mulgrave version:		4
Dimensions:	300 x 378 mm
Container(s):	Glass Vial
Supplier:	Howden Printing
Stock:	Primapharm 40gsm / Teropaque Thin Medical 40gsm
Folded dimensions:	31.5 x 150 mm
Printed both sides:	Yes
Perforated:	No
Pharma code:		71 (112111)
Pharma code length		9 mm
Mulgrave 4 series no.:		434471
Colours
Black:		■

ft

Hospira

Requester
I have checked this artwork against the registered text including spelling, layout, size, colours, registration numbers and scientific
equations, the name and address and
trademarks. Also for any possible changes to
related items.
This artwork is in conformance with the Marketing Authorisation and can now proceed
to the printing stage.
Previous Item Number: Q77025 / 434347
Signed:
Date:
Version 1		Version 2
Technician:	BE	Technician:	BE
Date:	21/Jul/14	Date:	21 /Jul/14
Version 3		Version 4
Technician:	LB	Technician:	LB
Date:	25/Jul/14	Date:	23/Oct/14
Version 5		Version 6
Technician:	LB	Technician:	EM
Date:	23/Oct/14	Date:	23/Oct/14
Version 7		Version 8
Technician:	JH	Technician:	JH
Date:	24/Oct/14	Date:	08/Jan/16
Version 9		Version 10
Technician:	JH	Technician:	XX
Date:	11/Feb/16	Date:	dd/mmm/yy