BALANCE 1.5% GLUCOSE, 1.75 mmol/L CALCIUM, PERITONEAL DIALYSIS SOLUTION

2. What you need to know before starting to use balance

Do not usebalance1.5% glucose, 1.75 mmol/l calcium

• if your blood potassium level is very low
• if your blood calcium level is very high
• if you have a metabolic disorder known as lactic acidosis

Peritoneal dialysis should not be started if you have:

• abdominal region alterationssuch as

• wounds, or after surgery
• burns
• extensive skin inflammatory reactions
• peritonitis
• uncured suppurating wounds
• umbilical, inguinal, or diaphragmatic hernias
• tumors in the abdomen or intestine

• inflammatory bowel diseases
• intestinal obstruction
• pulmonary disease, especially pneumonia
• generalized blood infection caused by bacteria
• very high levels of fat in the blood
• accumulation of toxins from urine in the blood, which cannot be eliminated by blood cleaning
• severe malnutrition and weight loss, especially if adequate protein intake is not possible.

Warnings and precautions

Inform your doctor immediately:

• in case of severe loss of electrolytes (salts)caused by vomiting and/or diarrhea.
• in case of abnormal kidneys(polycystic kidneys)
• in case of having peritonitis, recognizable because the peritoneal dialysis solution that comes out of your peritoneum is cloudy and/or abdominal pain. Show your doctor the bag containing the drainage solution.
• in case of severe abdominal pain, abdominal distension, or vomiting. This may be a sign of encapsulating peritoneal sclerosis, a complication of peritoneal dialysis treatment that can be life-threatening.

Peritoneal dialysis may cause loss of proteinsand water-soluble vitamins.

It is recommended to follow a suitable diet or take nutritional supplements to avoid deficiency states.

Your doctor should check the balance of electrolytes (salts), kidney function, body weight, and nutritional status.

Use ofbalancewith other medicines

Inform your doctor or pharmacist if you are using, have recently used, or may need to use any other medicine.

Peritoneal dialysis may alter the effect of some medicines, so your doctor may need to change the dose for some of them, especially the following:

• medicines for heart failure, such as digoxin.

Your doctor will check your blood potassium level and, if necessary, take appropriate measures.

• medicines that affect calcium levelssuch as those containing calcium or vitamin D.

• medicines that increase urine excretion, such as diuretics.
• medicinesadministered orally and that lower blood sugar levelsor insulin. Blood sugar levels should be regularly monitored. Diabetic patients may need to adjust their daily insulin dose.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor before using this medicine. There is no adequate data on the use of balancein pregnant or breastfeeding women. If you are pregnant or breastfeeding, you should use balanceonly if your doctor considers it absolutely necessary.

Driving and using machines

The influence of balanceon the ability to drive or use machines is negligible or non-existent.

3. How to use balance

Follow your doctor's instructions for administering this medicine exactly. If you are unsure, consult your doctor or pharmacist again.

Your doctor will determine the method, duration, and frequency of use, as well as the required volume of solution and the dwell time in the peritoneal cavity.

If you have tension in the abdominal region, your doctor may reduce the volume.

Continuous Ambulatory Peritoneal Dialysis (CAPD)

• Adults:The usual dose is between 2000-3000 ml of solution four times a day, depending on body weight and kidney function.

The solution is drained after a dwell time of between 2 and 10 hours.

• Children:The doctor will determine the required volume of dialysis solution based on tolerance, age, and body surface area.

The recommended initial dose is 600-800 ml/m2 of body surface area four times a day (up to 1000 ml/m2 at night).

Automated Peritoneal Dialysis (APD)

For this, the sleep•safeor Safe•Lock system is used. The bag exchange is controlled automatically by the cycler during the night.

• Adults:The normal prescription is 2000 ml (maximum 3000 ml) per exchange with 3-10 exchanges during the night and the cycler time of 8 to 10 hours, and one or two exchanges during the day.

• Children:The volume per exchange should be 800-1000 ml/m2 (up to 1400 ml/m2) of body surface area with 5-10 exchanges during the night.

Use balanceonly in the peritoneal cavity.

Use balanceonly if the solution is clear and the packaging is not damaged.

balanceis available in a double-chamber bag. Before using the solution in the two chambers, mix the solutions as described below.

Instructions for use:

Systemstay•safefor Continuous Ambulatory Peritoneal Dialysis (CAPD)

First, heat the bag with the solution to body temperature. This should be done using a suitable bag warmer. A 2000 ml bag at an initial temperature of 22°C will need about 120 minutes of warming time. You can obtain more detailed information in the manual of your warmer. To heat the solution, microwaves should not be used due to the risk of local overheating. The bag exchange can be carried out after warming the solution.

1. Preparation of the solution

Check the bag with the tempered solution (label, expiration date, transparency of the solution, integrity of the bag and overbag, integrity of the weld). Place the bag on a solid surface. Open the overbag of the bag and the disinfection cap. Wash your hands using an antimicrobial washing solution. Roll up the bag, which is placed horizontally on the overbag, from one of the lateral edges until the intermediate weld opens. The solutions from the two chambers mix automatically. Now roll up the bag from the top edge until the lower triangle weld is completely open. Check that all welds are completely open. Check that the solution is clear and that the bag has no leaks.

1. Preparation of the bag exchange

Hang the bag with the solution on the upper hanger of the infusion stand, unroll the tubes of the bag with the solution, and place the DISC connector in the organizer. After unrolling the tubes of the drainage bag, hang the bag on the lower hanger of the infusion stand. Place the catheter connector in one of the two connections of the organizer. Put the new disinfection cap on the remaining free connection. Disinfect your hands and remove the protective cap from the DISC connector. Connect the catheter connector to the DISC connector.

1. Outflow

Open the extension valve. The outflow starts.

Position ?

1. Purge

Once the outflow is complete, purge the drainage bag with new liquid (approximately 5 seconds).

Position ??

1. Inflow

Start the inflow by turning the rotary switch to the

Position ???

1. Safety step

Close the catheter extension by inserting the PIN into the catheter connector.

Position ????

1. Disconnection

Remove the protective cap from the new disinfection cap and screw it onto the old one. Unscrew the catheter connector from the DISC connector and screw it onto the new disinfection cap.

1. Closure of the DISC connector

Close the DISC connector with the open end of the used disinfection cap, which is placed in the right hole of the organizer.

1. Check the transparency and weight of the drained dialysate and if the effluent is clear, discard it.

Systemsleep•safefor Automated Peritoneal Dialysis (APD)

During automated peritoneal dialysis (APD), the cycler heats the solution automatically.

Systemsleep•safeof 3000 ml

1. Preparation of the solution:see system stay•safe
2. Unroll the tube of the bag

1. Remove the protective cap
2. Place the connector in the free port of the sleep•safe tray
3. The bag is ready for use with the sleep•safe equipment

Systemsleep•safeof 5000 and 6000 ml

1. Preparation of the solution

Check the bag with the solution (label, expiration date, transparency of the solution, integrity of the bag and overbag, integrity of the weld). Place the bag on a solid surface. Open the overbag of the bag. Wash your hands using an antimicrobial washing solution. Unfold the intermediate weld and the bag connector. Roll up the bag, which is placed horizontally on the overbag, from the diagonal end towards the bag connector. The intermediate weld will open. Continue until the weld of the small chamber also opens. Check that all welds are completely open. Check that the solution is clear and that the bag has no leaks.

1. – 5.: see the sleep•safe system of 3000 ml.

SystemSafe•Lockfor Automated Peritoneal Dialysis (APD)

During automated peritoneal dialysis (APD), the cycler heats the solution automatically.

1. Preparation of the solution: see the sleep•safe system of 5000 and 6000 ml
2. Remove the protective cap from the connector of the connection line.
3. Connect the lines to the bag.
4. Break the internal stop by bending the line and the PIN more than 90° on both sides.
5. The bag is ready for use.

The bags are for single use, and any unused solution should be discarded.

After proper training, balancecan be used independently at home. Make sure to follow all the steps you have learned during training and maintain adequate hygiene conditions when exchanging bags.

Always check the turbidity of the drained dialysate. See section 2.

If you use morebalancethan you should

If you infuse an excess of dialysis solution into the peritoneal cavity, it can be drained. If you use too many bags, contact your doctor, as it may cause electrolyte and/or fluid imbalance.

In case of overdose or accidental ingestion, consult your doctor or pharmacist or call the Toxicology Information Service, phone 91 562 04 20, indicating the medicine and the amount ingested.

If you forget to usebalance

Try to reach the total prescribed volume for each 24-hour period to avoid consequences that may put your life at risk. You should consult your doctor if you have doubts.

If you have any other questions about the use of this medicine, ask your doctor, pharmacist, or nurse.

4. Possible side effects

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

You may experience the following side effects as a result of peritoneal dialysis treatment in general:

very common (may affect more than 1 in 10 people)

• peritonitis, which is noticed by a cloudy dialysate drainage solution coming out of your peritoneum, abdominal pain, fever, discomfort, or, in very rare cases, blood infection.

Show your doctor the bag containing the drainage solution.

• skin inflammation at the catheter exit site or along the length of the catheter, recognizable by redness, swelling, pain, exudation, or crusts.
• hernia in the abdominal wall

Contact your doctor immediately if you experience any of these side effects.

Other side effects of the treatment are the following:

common (may affect up to 1 in 10 people)

• problems with the entry or exit of the dialysate
• feeling of stretching or fullness of the abdomen
• shoulder pain

uncommon (may affect up to 1 in 100 people)

• diarrhea
• constipation

very rare(may affect up to 1 in 10,000 people)

• blood infection

not known(frequency cannot be estimated from the available data)

• breathing difficulties
• discomfort
• encapsulating peritoneal sclerosis, whose symptoms could be abdominal pain, abdominal distension, or vomiting

You may experience the following side effects when using balance:

very common(may affect more than 1 in 10 people)

• potassium deficiency

common (may affect up to 1 in 10 people)

• excess calcium if the ingested calcium is too high
• high blood sugar levels
• high levels of fat in the blood
• weight gain

uncommon (may affect up to 1 in 100 people)

• body fluid level too low, which can be recognized by rapid weight loss, decreased blood pressure, rapid pulse.
• body fluid level too high, which can be recognized by the presence of water in tissues and lungs, high blood pressure, breathing difficulties.
• dizziness

Reporting of side effects

If you experience any side effects, consult your doctor, pharmacist, or nurse, even if they are not listed in this leaflet. You can also report them directly through the Spanish Medicines Monitoring System for Human Use: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of balance

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

Do not use this medicine after the expiration date stated on the bag and carton after EXP. The expiration date is the last day of the month indicated.

Do not store at a temperature below 4°C.

The ready-to-use solution should be used immediately, within 24 hours after mixing.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. This will help protect the environment.

6. Container Content and Additional Information

Composition ofbalance

• The active principles in one liter of ready-to-use solutionare:

Calcium chloride dihydrate 0.2573 g

Sodium chloride 5.640 g

Sodium (S)-lactate solution 7.85 g

(3.925 g sodium (S)-lactate)

Magnesium chloride hexahydrate 0.1017 g

Glucose monohydrate 16.5 g

(15.0 g anhydrous glucose)

These amounts of active substance are equivalent to:

1.75 mmol/l calcium, 134 mmol/l sodium, 0.5 mmol/l magnesium, 101.5 mmol/l chloride, 35 mmol/l lactate, and 83.2 mmol/l glucose.

The other components are water for injectable preparations, hydrochloric acid, sodium hydroxide, and sodium bicarbonate.

Appearance of the Product and Container Content

The solution is transparent and colorless.

The theoretical osmolarity of the ready-to-use solution is 358 mOsm/l, and the pH is approximately 7.0.

balanceis available in double-chamber bags. One chamber contains the alkaline sodium lactate solution, and the other chamber contains the acidic glucose solution with electrolytes.

balanceis available in the following application systems and container sizes:

Only some container sizes may be marketed.

Marketing Authorization Holder:

Fresenius Medical Care Deutschland GmbH, Else-Kröner-Straße 1, 61352 Bad Homburg v.d.H. Germany

Manufacturer:

Fresenius Medical Care Deutschland GmbH, Frankfurter Straße 6-8, 66606 St. Wendel Germany

Local Representative:

Fresenius Medical Care España S.A.

C/ Ronda de Poniente, 8, ground floor, Parque Empresarial Euronova,

28760 Tres Cantos (Madrid)

Spain

This medicinal product is authorized in the Member States of the European Economic Area under the following names:

See the end of this multilingual prospectus.

Date of the last revision of this prospectus: 01/2020

Detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/.