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The product code(s) for this leaflet is: PL 00116/0338.
Potassium Chloride 0.15 % w/v and Glucose 5% w/v Solution for Infusion -BP
Potassium Chloride 0.15% w/v & Glucose 5% w/v Solution for Infusion BP
Active substances: potassium chloride and glucose monohydrate
1. What Potassium 0.15 & Glucose Infusion is and what it is used for
2. What you need to know before you are given Potassium 0.15 & Glucose Infusion
3. How you will be given Potassium 0.15 & Glucose Infusion
4. Possible side effects
5. How to store Potassium 0.15 & Glucose Infusion
6. Content of the pack and other information
Potassium 0.15 & Glucose Infusion is a solution of potassium chloride and glucose in water. Potassium chloride is a chemical substance (often called a “salt”) found in the blood. Glucose is one of the body’s sources of energy. This solution for infusion provides 200 kilocalories per litre.
Potassium 0.15 & Glucose Infusion is used as a source of carbohydrate (sugar) in the prevention and treatment of:
Please tell your doctor if you have or have had any of the following medical conditions:
When you are given this infusion, your doctor will take blood and urine samples and monitor:
Your doctor will take into account if you are receiving parenteral nutrition (nutrition given by infusion into a vein). During long term treatment with Potassium 0.15 & Glucose Infusion you may need to be given extra nutrition
As Potassium 0.15 & Glucose Infusion contains sugar (glucose), it can cause a high level of sugar in the blood (hyperglycaemia). If this occurs, your doctor may:
This is particularly important if you are diabetic.
Potassium 0.15 & Glucose Infusion should be given with special care in children.
In newborns, especially born premature and with low birth weight are at increased risk of developing a too low or too high level of sugar in the blood (hypo or hyperglycemia) due to infusion of glucose solutions.
Low level of sugar in the newborn can cause prolonged seizures, coma and brain damage. High level of sugar has been associated with bleeding into the brain, late onset bacterial and fungal infection, infection in the intestinal track (necrotizing enterocolitis), affects eyes (retinopathy of prematurity), lungs problems (bronchopulmonary dysplasia), prolonged length of hospital stay, and death.
Pediatric patients should be closely monitored. In cases where normal regulation of the water content of the blood is disturbed due to increased secretion of Antidiuretic Hormone (ADH), the infusion of fluids with a low concentration of sodium chloride (hypotonic fluids) may result in a low level of sodium in the blood (hyponatraemia). This can lead to headache, nausea, seizures, lethargy, coma, swelling of the brain (cerebral oedema) and death; therefore these symptoms (acute symptomatic hyponatraemic encephalopathy) are considered a medical emergency.
Tell your doctor or nurse if you are taking, have recently taken or might take any other medicines.
It is particularly important that you inform your doctor if you are taking medicines that increase the concentration of potassium in the blood, such as:
Some medicines act on the hormone vasopressin. These may include:
Potassium 0.15 & Glucose Infusion must not be added or given through the same needle with citrate anticoagulated/preserved blood. This can damage the red blood cells or cause them to clump together.
You should ask your doctor about what you can eat or drink.
Ask your doctor or nurse for advice before taking this medicine.
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or nurse for advice before taking this medicine.
Changes in the potassium levels in your blood can affect how well your heart and your unborn baby’s heart work. Your doctor will therefore carefully monitor the levels of the chemicals in your blood.
Potassium 0.15 & Glucose Infusion can be given during pregnancy. The amount you are given must be carefully controlled by your doctor.
However, if another medicine is to be added to your solution for infusion during pregnancy or breast-feeding you should:
Potassium 0.15 & Glucose Infusion does not affect your ability to drive or use machines.
Potassium 0.15 & Glucose Infusion will be given to you by a doctor or nurse. Your doctor will decide on how much you need and when it is to be given. This will depend on your age, weight, condition, state of hydration (the amount of water in your body) and the reason for treatment. The amount you are given may also be affected by other treatments you are receiving.
You should NOT be given Potassium 0.15 & Glucose Infusion if there are particles floating in the solution or if the pack is damaged in any way.
The speed of infusion will be decided by your doctor.
If you require a large volume or rapid infusion of Potassium 0.15 & Glucose Infusion, your doctor may monitor your ECG (heart tracing).
Potassium 0.15 & Glucose Infusion will usually be given to you through a plastic tube attached to a needle in a vein. Usually a vein in your arm is used to give you the infusion. However, your doctor may use another method to give you the medicine.
Before and during the infusion, your doctor will monitor:
If you suffer from poor kidney function, you may receive a lower dose.
Any unused solution should be thrown away. You should NOT be given an infusion of Potassium 0.15 & Glucose Infusion from a bag that has been partly used.
If you are given too much Potassium 0.15 & Glucose Infusion (over-infusion), or you are given your infusion too quickly, this may lead to the following symptoms:
If you develop any of these symptoms you must inform your doctor immediately. Your infusion will be stopped and you will be given treatment depending on the symptoms.
If a medicine has been added to your Potassium 0.15 & Glucose Infusion before over-infusion occurs, that medicine may also cause symptoms. You should read the Package Leaflet of the added medicine for a list of possible symptoms.
Your doctor will decide when to stop giving you this infusion.
If you have any further questions on the use of this product, ask your doctor.
Like all medicines, Potassium 0.15 & Glucose Infusion can cause side effects, although not everybody gets them.
The side effects that may occur due to the administration technique include:
Low levels of sodium in the blood that may be acquired during hospitalization (nosocomial hyponatraemia) and related neurological disorders (acute hyponatremic encephalopathy). Hyponatraemiacan lead to irreversible brain injury and death due to cerebral oedema/swelling (see also in section 2 “warnings and precautions”)
If you get any side effects talk to your doctor or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting options below. By reporting side effects you can help provide more information on the safety of this medicine.
Ireland
Malta
United Kingdom
Keep this medicine out of the sight and reach of children.
Potassium 0.15 & Glucose Infusion does not require special storage conditions.
Potassium 0.15 & Glucose Infusion should NOT be given to you after the expiry date which is stated on the bag after EXP. The expiry date refers to the last day of that month.
You should not be given Potassium 0.15 & Glucose Infusion, if there are particles floating in the solution or if the unit is damaged in any way.
The active substances are:
The other ingredients are
Potassium 0.15 & Glucose Infusion is a clear solution, free from visible particles. It is supplied in polyolefin/polyamide plastic bags (Viaflo). Each bag is wrapped in a sealed, protective, outer plastic overpouch.
The bag sizes are:
The bags are supplied in cartons. Each carton contains one of the following quantities:
Not all pack sizes may be marketed
Marketing Authorisation Holder :
United Kingdom
Ireland and Malta
Manufacturers for Great Britain:
Manufacturers for Ireland:
This leaflet was last revised in June 2023
For information about Potassium 0.15 & Glucose Infusion or to request this leaflet in formats such as audio or large print please contact the Marketing Authorisation Holder: Tel: + 44 (0) 1635 206345.
Baxter and Viaflo are trademarks of Baxter International lnc.
TH-30-02-216