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Osate 4 Mg/5 Ml Concentrate For Solution For Infusion

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Osate 4 mg/5 ml

concentrate for solution for infusion

Zoledronic acid


PACKAGE LEAFLET:

INFORMATION FOR THE PATIENT

Osate 4 mg/5 ml concentrate for solution for infusion

Zoledronic acid

Read all of this leaflet carefully before you are given this medicine because it contains important information for you.

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

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

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


What is in this leaflet:

1.    What Osate is and what it is used for

2.    What you need to know before you are given Osate

3.    How to use Osate

4.    Possible side effects

5.    How to store Osate

6.    Contents of the pack and other information

1.    WHAT IS OSATE AND WHAT IS IT USED FOR

The active substance of Osate is zoledronic acid, which belongs to a group of substances called bisphosphonates. Zoledronic acid works by attaching itself to the bone and slowing down the rate of bone change. It is used:

   To prevent bone complications, e.g. fractures, in adult patients with bone metastases (spread of cancer from primary site to the bone).

   To reduce the amount of calcium

in the blood in adult patients where it is too high due to the presence of a tumour. Tumours can accelerate normal bone change in such a way that the release of calcium from bone is increa sed. This condition is known as tumour-induced hyper-calcaemia (TIH).

Osate will always be given to you by a doctor or a nurse as an infusion in a vein.

2.    WHAT YOU NEED TO KNOW BEFORE YOU ARE GIVEN OSATE

Follow carefully all instructions given to you by your doctor.

Your doctor will carry out blood tests before you start treatment with Osate and will check your response to treatment at regular intervals.

You should not be given Osate:

•    if you are allergic to zoledronic acid, another bisphosphonate (the group of substances to which Osate belongs), or any of the other ingredients of this medicine (listed in section 6.1)

•    if you are breast-feeding. Warnings and precautions

Talk to your doctor or nurse before you are given Osate:

•    if you have or have had a kidney problem

•    if you have or have had pain, swelling or numbness of the

jaw, a feeling of heaviness in the jaw or loosening of a tooth

•    if you are having dental treatment or are due to undergo dental surgery, tell your dentist that you are being treated with Osate

•    if you have any pain in your thigh, hip or groin. It is also important that you tell your doctor if you experience this after starting treatment with Osate (see section 4).

Children and adolescents Osate is not recommended for use in children and adolescents below the age of 18 years.

Patients aged 65 years and over Osate can be given to people aged 65 years and over. There is no

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evidence to suggest that any extra precautions are needed.

Other medicines and Osate

Tell your doctor if you are taking or have recently taken any other medicines. It is especially important that you tell your doctor if you are also taking:

•    Aminoglycosides (medicines used to treat severe infections), since the combination of these with bisphosphonates may cause the calcium level in the blood to become too low

•    Thalidomide (a medicine used to treat a certain type of blood cancer involving the bone) or any other medicines which may harm your kidneys

•    Other medicines that also contains zoledronic acid and is used to treat osteoporosis and other non-cancer diseases of the bone, or any other bisphosphonate, since the combined effects of these medicines taken together with Osate are unknown

•    Anti-angiogenic medicines (used to treat cancer), since the combination of these with Osate has been associated with reports of osteonecrosis of the jaw (ONJ).

Pregnancy, breast-feeding and fertility

You should not be given Osate if you are pregnant. Tell your doctor if you are or think that you may be pregnant.

You must not be given Osate if you are breast-feeding.

If you are pregnant or breastfeeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine.

Driving and using machines

There have been very rare cases of drowsiness and sleepiness with the use of Osate. You should therefore be careful when driving, using machinery or performing other tasks that need full attention.

Important information about some of the ingredients in Osate

This medicine contains less than 1 mmol sodium (23 mg) per vial, i.e. essentially sodium-free.

3. HOW OSATE IS GIVEN

•    Osate must only be given by healthcare professionals trained in administering bisphosphonates intravenously, i.e. through a vein

•    Your doctor will recommend that you drink enough water before each treatment to help prevent dehydration

•    Carefully follow all the other instructions given to you by your doctor, nurse or pharmacist.

How much Osate is given

•    The usual single dose given is 4 mg

•    If you have a kidney problem, your doctor will give you a lower dose depending on the severity of your kidney problem.

How often Osate is given

•    If you are being treated for the prevention of bone complications due to bone metastases, you will be given one infusion of Osate every three to four weeks

•    If you are being treated to reduce the amount of calcium in your blood, you will normally only be given one infusion of Osate.

How Osate is given

•    Osate is given as a drip (infusion) into a vein which should take at least 15 minutes and should be administered as a single intravenous solution in a separate infusion line.

Patients whose blood calcium levels are not too high will also be prescribed calcium and vitamin D supplements to be taken each day.    .../...


THE FOLLOWING INFORMATION IS INTENDED FOR HEALTHCARE PROFESSIONALS ONLY:


How to prepare and administer Osate

To prepare an infusion solution containing 4 mg zoledronic acid, further dilute the Osate concentrate (5.0 ml) with 100 ml of calcium-free or other divalent cation-free infusion solution. If a lower dose of Osate is required, first withdraw the appropriate volume as indicated below and then dilute it further with 100 ml of infusion solution. To avoid potential incompatibilities, the infusion solution used for dilution must be either 0.9% w/v sodium chloride or 5% w/v glucose solution.

Do not mix Osate concentrate with calcium-containing or other divalent cation-containing solutions such as lactated Ringer's solution.


Instructions for preparing reduced doses of Osate:

Withdraw the appropriate volume of the liquid concentrate, as follows:

•    4.4 ml for 3.5 mg dose

•    4.1 ml for 3.3 mg dose

•    3.8 ml for 3.0 mg dose

For single use only. Any unused solution should be discarded. Only clear solution free from particles and discolouration should be used. Aseptic techniques must be followed during the preparation of the infusion.

Chemical and physical in-use stability has been demonstrated for 24 hours at 2°C -    8°C;

however from a microbiological point of view, the diluted solution for infusion should be used immediately. If not used immediately, in-use storage times and


If you are given more Osate than

• Sudden coldness with fainting,

you should

limpness or collapse

If you have received doses higher

• Difficulty in breathing with

than those recommended, you

wheezing or coughing

must be carefully monitored by

• Urticaria.

your doctor. This is because you

Rare side effects

may develop serum electrolyte

(may affect up to 1 in 1.000

abnormalities (e.g. abnormal

people):

levels of calcium, phosphorus

• Slow heartbeat

and magnesium) and/or changes

• Confusion

in kidney function, including

• Unusual fracture of the thigh

severe kidney impairment.

bone particularly in patients on

If your level of calcium falls too

long-term treatment for

low, you may have to be given

osteoporosis may occur rarely.

supplemental calcium by

Contact your doctor if you

infusion;

experience pain, weakness or

If you have any further questions

discomfort in your thigh, hip or

on the use of this medicine, ask

groin as this may be an early

your doctor or nurse.

indication of a possible fracture of the thigh bone

4. POSSIBLE SIDE EFFECTS

• Interstitial lung disease

Like all medicines, this medicine

(inflammation of the tissue

can cause side effects, although

around the air sacks of the

not everybody gets them. The

lungs)

most common ones are usually

Very rare side effects (may affect

mild and will probably disappear

up to 1 in 10.000 people):

after a short time.

• Fainting due to low blood

Tell your doctor about any of the

pressure

following serious side effects

• Severe bone, joint and/or

straight away:

muscle pain, occasionally

Common side effects

incapacitating

(may affect up to 1 in 10 people):

• Painful redness and/or swelling

• Severe kidney impairment

of the eye.

(will normally be determined by

If you get any side effects, talk to

your doctor with certain

your doctor or nurse. This

specific blood tests);

includes any possible side

• Low level of calcium in the

effects not listed in this leaflet.

blood.

You can also report side effects

Uncommon side effects

directly via Yellow Card Scheme,

(may affect up to 1 in 100 people):

Tel: Freephone 0808 100 3352

• Pain in the mouth, teeth and/or

Website:

jaw, swelling or sores inside the

www.mhra.gov.uk/yellowcard.

mouth, numbness or a feeling of

By reporting side effects you can

heaviness in the jaw, or

help provide more information on

loosening of a tooth. These could be signs of bone damage

the safety of this medicine.

in the jaw (osteonecrosis). Tell

5. HOW TO STORE OSATE

your doctor and dentist

Your doctor, nurse or pharmacist

immediately if you experience

knows how to store Osate

such symptoms

properly.

• Irregular heart rhythm (atrial

Keep this medicine out of the

fibrillation) has been seen in

sight and reach of children.

patients receiving zoledronic

Do not throw away any medicines

acid for postmenopausal

via wastewater. Ask you

osteoporosis. It is currently

pharmacist how to throw away

unclear whether zoledronic

medicines you no longer use.

acid causes this irregular heart

These measures will help protect

rhythm but you should report it

the environment.

to your doctor if you experience

Do not use this medicine after the

such symptoms after you have

expiry date which is stated on the

received zoledronic acid

carton and vial label after EXP.

• Severe allergic reaction:

The expiry date refers to the last

shortness of breath, swelling

day of that month.

mainly of the face and throat.

This medicine does not require

Tell your doctor about any of the

any special storage conditions

following side effects as soon as

until the vial has been opened and

possible:

Very common side effects

the concentrate is diluted.

(may affect more than 1 in 10

6. CONTENTS OF THE PACK AND

people):

OTHER INFORMATION

• Low level of phosphate in the

What Osate contains

blood.

• The active substance of Osate

Common side effects

is zoledronic acid. One vial

(may affect up to 1 in 10 people):

contains 4 mg zoledronic acid,

• Headache and a flu-like

corresponding to 4.264 mg

syndrome consisting of fever,

zoledronic acid monohydrate

fatigue, weakness, drowsiness,

(as monohydrate),

chills and bone, joint and/or

corresponding to 4.264 mg

muscle ache. In most cases no

zoledronic acid monohydrate.

specific treatment is required

• The other ingredients are:

and the symptoms disappear

mannitol, sodium citrate, water

after a short time (couple of

for injections.

hours or days)

What Osate looks like and

• Gastrointestinal reactions such

contents of the pack

as nausea and vomiting as well

Osa te is supplied as a liquid

as loss of appetite

concentrate in a vial. One vial

• Conjunctivitis

contains 4 mg of zoledronic acid.

• Low level of red blood cells

Each pack contains the vial with

(anaemia).

concentrate. Osate is supplied as

Uncommon side effects

packs containing 1, 4 or 10 vials.

(may affect up to 1 in 100 people):

Not all pack sizes may be

• Hypersensitivity reactions

marketed.

• Low blood pressure

Marketing Authorisation Holder

• Chest pain

and Manufacturer

• Skin reactions (redness and

Marketing Authorisation Holder

swelling) at the infusion site,

STRAGEN UK Ltd

rash, itching

Castle Court, 41 London Road

• High blood pressure, shortness

Reigate, Surrey RH2 9RJ

of breath, dizziness, sleep

Phone: +44 (0)870 351 87 44

disturbances, tingling or

Email: info@stragenuk.com

numbness of the hands or feet,

Manufacturer

diarrhoea

Lisa Pharma

• Low counts of white blood cells

Via Licinio 11, 22036 ERBA (Como)

and blood platelets • Low level of magnesium and

Italy

potassium in the blood. Your

This leaflet was last revised in

doctor will monitor this and take any necessary measures • Sleepiness

04/2013

• Tearing of the eye, eye

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1

1

1

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1

1

1

1

1

sensitivity to light

conditions prior to use are the

Since no data are available on the

responsibility of the user and

compatibility of Osate with other

would normally not be longer than

intravenously administered substan-

24 hours at 2°C - 8°C.

ces, Osate must not be mixed with

The refrigerated solution should

other medications/substances and

then be equilibrated to room

should always be given through a

temperature prior to administration.

separate infusion line.

The solution containing zoledronic

How to store Osate

acid is given as a single 15-minute

• Keep Osate out of the sight and

intravenous infusion in a separate

reach of children

infusion line. The hydration status

• Do not use Osate after the

of patients must be assessed

expiry date stated on the pack

prior to and following adminis-

• The unopened vial does not

tration of Osate to ensure that

require any specific storage

they are adequately hydrated.

conditions

Studies with several types of

• The diluted Osate infusion

infusion lines made from

solution should be used

polyvinylchloride, polyethylene

immediately in order to avoid

and polypropylene showed no incompatibility with Osate.

microbial contamination.