Document: leaflet MAH BRAND_PL 03551-0067 change

• leaflet MAH BRAND_PL 00116-5048R
• leaflet MAH BRAND_PL 03551-0067
• leaflet MAH BRAND_PL 12580-0020

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95/12260872/0714

What is in this leaflet:

1.    What Compound Sodium Lactate is and what it is used for

2.    What you need to know before you use Compound Sodium Lactate

3.    How to use Compound Sodium Lactate

4.    Possible side effects

5.    How to store Compound Sodium Lactate

6.    Contents of the pack and other information

1. What Compound Sodium Lactate is and what it is used for

Compound Sodium Lactate is a solution for supply of fluid and salts to the body. It is supplied to you through a vein drip (an infusion). Its salt composition is similar to that of human blood.

You will receive this solution if

•    you need to receive fluids and salts. This applies when your acid-base balance is normal or your blood is a little bit too acidic (mild acidosis)

•    you have lost water

•    you have lost water and salts

•    you have lost blood and need this replaced for a short time

•    your doctor wants to give you salts or some drugs that need to be dissolved or diluted.

2. What you need to know before you use Compound Sodium Lactate

Do not use Compound Sodium Lactate if you have

•    an impairment to metabolise lactate connected with high levels of lactate in your blood (see also section "Take special care with...")

•    too much water in your body (water intoxication)

•    too high blood volume (circulatory overload)

•    a weak heart that can not pump enough blood into your lungs or circulation (congestive heart failure)

•    abnormally high blood pressure (hypertension)

•    impaired kidney function

•    severe liver damage

•    an accumulation of fluid and sodium (oedema with sodium retention)

•    too alkaline blood due to hyperventilation (respiratory alkalosis)

Your doctor will not give you this medicine to correct abnormally high levels of acids in the blood caused by your metabolism (severe metabolic acidosis)

Warnings and precautions

Your doctor will exercise particular caution if you have

•    lost water while retaining the salts

•    too high blood levels of potassium, sodium, calcium or chloride

•    abnormally high levels of bases in the blood caused by your metabolism (severe metabolic alkalosis)

•    failure of your lungs

•    excess water in your body (peripheral oedema)

•    a condition where you are retaining sodium, such as high blood pressure, toxaemia of pregnancy (see "Pregnancy and breast-feeding"), too high levels of aldosterone in your body, treatment with cortisone

•    a condition where you are retaining potassium, e.g. acute deficiency of water in your body, extensive tissue destruction as occurs with severe burns

•    a disease associated with high levels of vitamin D in your blood such as sarcoidosis

•    kidney stones or a history of them

If you have constantly low blood sodium levels your doctor will take special care to give you this solution slowly. This will prevent possible brain damages (osmotic demyelinisation syndrome).

Children

Your doctor will take special care of your child aged less than 3 months if he/ she receives this solution.

Use as vehicle solution

Please note: If this solution is used as vehicle solution the safety information of the additive provided by the respective manufacturer has to be taken into account.

While you receive this solution the following parameters will be checked to ensure that these are normal:

•    your blood salt and lactate levels

•    your acid-base balance

•    your fluid balance

Other medicines and Compound Sodium Lactate

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

Your doctor will administer this solution to you only with caution if you are taking

•    cortisone or carbenoxolone

•    medicines for the treatment of heart weakness (e.g. digitalis preparations, digoxin).

•    medicines that cause an increase of your serum potassium level (see the list below).

-    medicines that increase your urine flow and retain potassium (e.g. tri-amteren, amilorid, spironolactone, alone or in association)

-    medicines that are used for the treatment of high blood pressure (ACE inhibitors, e.g. captopril, enalapril; Angiotensin II receptor antagonists, eg. valsartan, losartan)

-    some drugs that are used to suppress your immune system (e.g. tacrolimus, cyclosporine)

-    a special drug called suxamethonium used to relax your muscles

•    simultaneously thiazid-diuretics and vitamin D

•    concomitantly medicines for the treatment of brittle bone disease (e.g. bisphosphonates, fluorides) or specific antibiotics (e.g. fluorchinolones, tetracyclines)

•    stimulating medicinal products (e.g. ephedrine, pseudoephedrine, desam-phetaminesulphate, fenfluramine hydrochloride).

Lactate leads to an alkalinisation of your urine. This may change the excretion of certain drug substances (e.g. salicylic acid).

Some drugs must not be mixed with Compound Sodium Lactate. These include drugs containing oxalate, phosphate or carbonate/bicarbonate. Doctors only add drugs to Compound Sodium Lactate if they are sure they are safe to mix.

Incompatibility has been reported with novobiocin sodium, oxytetracycline hydrochloride, sodium bicarbonate, sodium calcium edetate, and sulphadi-azine sodium.

Pregnancy and breast-feeding

Ask your doctor or pharmacist for advice before taking or using any medicine. Pregnancy

If you are pregnant, please inform your doctor. Your doctor will administer this solution to you only if he thinks it is necessary.

Your doctor will exercise particular caution if you have toxaemia of pregnancy. This is a condition of the third trimester when the patient has the following symptoms:

•    high blood pressure

•    swelling of body tissues

•    protein in the urine.

Breast-feeding

Calcium is excreted in human milk, but at therapeutic doses of Compound Sodium Lactate no effects on the breastfed newborns/infants are anticipated. Therefore Compound Sodium Lactate can be used during breast-feeding.

Driving and using machines

This medicine has no influence on the ability to drive and use machines.

3. How to use Compound Sodium Lactate Dosage

This medicine will be administered to you by a doctor or health-care professional.

The doctor will decide the right dose of Compound Sodium Lactate depending on your fluid and electrolyte requirements. Thus your age, weight, clinical condition and physiological (acid-base) status will be taken into account.

BlBRAUN

The recommended dosages are:

Adults and adolescents

Maximum daily dose

Normal fluid requirements are met with 40 ml per kg body weight per day. Your doctor may determine individual adaptation of the dose and infusion

Maximum infusion rate:

The infusion rate will be adjusted according to your clinical condition. The infusion rate should normally not exceed the following values:

5 ml per kg body weight per hour Children

The dose is adjusted according to the individual requirements of fluid and electrolytes. Thus the patient's age, weight, clinical and biological (acid-base balance) conditions and concomitant therapy should be taken into account.

Elderly patients

Basically the same dosage as for adults applies, but caution will be exercised if you are suffering from further diseases like heart weakness that may frequently be associated with advanced age.

Patients with burns Adults

During the first 24 hours you will receive 4 ml of solution per kg per percent burn.

Children

During the first 24 hours your child will receive 4 ml of solution per kg per percent burn. Thus the following volume is added as maintenance for children according to his/her weight

-    for children weighing 0 - 10 kg the amount is 4 ml per kg body weight per hour;

-    for children weighing 10 - 20 kg the amount is 40 ml per h + 2 ml per kg body weight per hour;

-    for children weighing more than 20 kg, the amount is 60 ml per h + 1 ml per kg body weight per hour.

Use as vehicle solution

If Compound Sodium Lactate is used as vehicle solution for compatible electrolyte concentrates and medicinal products, the instructions for use relating to the medicinal product to be added will be observed.

If you use more Compound Sodium Lactate than you should

An overdose may lead to hyperhydration (excess fluid in the body), which will be followed by

•    increased skin tension,

•    congestion in your veins,

•    swelling of body tissues

•    water on the lungs or in your brain

•    disorders of your fluid, salt and acid-base balance,

•    high salt levels in your blood.

If an overdose occurs, your doctor will give you any necessary treatment.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowca rd.

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

5. How to store Compound Sodium Lactate

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 label. The expiry date refers to the last day of that month.

This medicinal product does not require any special storage conditions.

Containers are for single-use only. Discard container and any unused content after use.

No special requirements for disposal. Only to be used if the solution is clear, colourless and the container and its closure do not show visible signs of damage.

Do not reconnect partially used containers.

6. Contents of the pack and other information

What Compound Sodium Lactate contains

•    The active substances:

1000 ml of the solution contain Sodium chloride

Sodium lactate solution (50% w/w)

(equivalent to sodium lactate, 3.12 g) Potassium chloride Calcium chloride dihydrate

Electrolyte concentrations:

Sodium

Potassium

Calcium

Chloride

Lactate

•    The other ingredient is Water for injections

Theoretical osmolarity:

Titration acidity: pH:

What Compound Sodium Lactate looks like and contents of the pack

It is a solution for infusion, i.e. for administration by a vein drip.

It is a clear, colourless solution of salts in water.

It comes in

•    polyethylene bottles containing 500 ml or 1000 ml, available in packs of 10 x 500 ml and 10 x 1000 ml

•    plastic bags containing 500 ml or 1000 ml, available in packs of 20 x 500 ml and 10 x 1000 ml

Not all pack sizes may be marketed

4. Possible side effects

Like all medicines, Compound Sodium Lactate can cause side effects, although not everybody gets them.

However, it is unlikely that any adverse effect occurs as long as this medicine is used as directed.

Yet, if you notice any side effects, please tell your doctor or pharmacist. Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can

Marketing authorisation holder and manufacturer

B. Braun Melsungen AG

Carl-Braun-StraBe 1, 34212 Melsungen, Germany

Postal address

34209 Melsungen, Germany Phone: +49-5661-71-0 Fax:    +49-5661-71-4567

This leaflet was last revised in May 2014.

The following information is only intended for health-care professionals:

Special warnings and precautions for use

Lactate utilisation may be impaired in the presence of hypoxia or hepatic insufficiency.

Compound sodium lactate contains an amount of potassium that is similar to that of the physiological concentration of potassium in human blood. Nevertheless it is not suitable for the treatment of patients with severe potassium deficiency.

As the solution contains metabolisable ions (e.g. lactate) it may cause metabolic alkalosis.

Care should be taken to prevent extravasation during intravenous infusion.

In case of concomitant blood transfusion, the solution must not be administered via the same infusion set.

If lactate accumulates during infusion, the dosage and infusion rate should be reduced or administration of the solution should eventually be discontinued. Important information about the container

The plastic container contains a significant volume of air. To avoid risk of air embolism, all air must be expelled before starting a pressure infusion. Treatment of overdose:

Cessation of infusion, administration of diuretics with continuous monitoring of serum electrolytes, correction of electrolyte and acid-base imbalances.

In severe cases of overdose dialysis may be necessary.

Shelf life after admixture of additives

From the 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.

B BRAUN

B. Braun Melsungen AG

34209 Melsungen, Germany

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