- Brand name
- Plasma-Lyte 148 and 5% Glucose IV Infusion
- Active ingredient
- Sodium chloride; Sodium gluconate; Sodium acetate; Potassium chloride; Magnesium chloride hexahydrate; Glucose
Consumer medicine information (CMI) leaflet
Please read this leaflet carefully before you start using Plasma-Lyte 148 and 5% Glucose IV Infusion.Download CMI (PDF) Download large text CMI (PDF)
What is in this leaflet
This leaflet answers some common questions about Plasma-Lyte 148 and 5% Glucose Replacement Infusion. It does not contain all of the available information. It does not take the place of talking to your doctor, nurse or pharmacist.
All medicines have risks and benefits. Your doctor has weighed the risks of you using this product against the benefit they expect it will have for you.
If you have any concerns about being given this medicine, ask your doctor, nurse or pharmacist.
What Plasma-Lyte 148 and 5% Glucose Replacement Infusion is used for
Plasma-Lyte 148 and 5% Glucose Replacement Infusion is a solution used as a source of water, electrolytes (salts) and calories.
Ask your doctor if you have any questions about why this medicine has been prescribed for you.
Your doctor may have prescribed it for another reason.
Before you start Plasma-Lyte 148 and 5% Glucose Replacement Infusion
When you must not be given it
Plasma-Lyte 148 Replacement and 5% Glucose Infusion must not be given to you if:
- you have an allergy to any ingredient listed at the end of this leaflet;
- you have had an allergic reaction to corn or corn products. Some of the symptoms of an allergic reaction may include skin rash, peeling of the skin and swelling of the face, lips or tongue, causing difficulty swallowing or shortness of breath;
- the expiry date printed on the pack has passed.
You must tell your doctor if you have or have had any of the following medical conditions:
- heart failure;
- respiratory failure (lung disease);
- severe kidney failure;
- high blood pressure (hypertension);
- build up of fluid under the skin, particularly around the ankles (peripheral oedema);
- build up of fluid in the lungs (pulmonary oedema);
- high blood pressure during pregnancy (pre-eclampsia or eclampsia)
- aldosteronism (a disease that causes high levels of hormone called aldosterone);
- any other condition associated with retaining sodium or fluid , such as treatment with steroids;
- diabetes (your blood sugar levels will be monitored closely and your insulin treatment may need to be modified);
- any condition that means you are more likely to have high blood levels of potassium (hyperkalaemia), such as kidney failure, adrenocortical insufficiency, severe dehydration (a loss of water from the body, eg. due to vomiting or diarrhoea) or extensive tissue damage (as can occur in severe burns) – your doctor will need to check your blood potassium levels;
- myasthenia gravis (a disease that causes progressive muscle weakness);
- recovery after an operation;
- head injury within the past 24 hours;
- a high pressure within the skull (intracranial hypertension);
- a stroke;
- are pregnant;
- are breast-feeding.
Taking other medicines
Tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including any that you get without a prescription from your pharmacy, supermarket or health food shop.
Some medicines may interfere with Plasma-Lyte 148 and 5% Glucose Replacement Infusion. These include:
- potassium-sparing diuretics (certain water tablets, eg. amiloride, spironolactone, triamterene);
- angiotensin converting enzyme (ACE) inhibitors (used to treat high blood pressure);
- tacrolimus (used to prevent rejection of a transplant and to treat some skin diseases);
- cyclosporin (used to prevent rejection of a transplant);
These medicines can increase the concentration of potassium in your blood. This can be life-threatening. A rise in your blood potassium levels is more likely to occur if you have kidney disease.
- corticosteroids (anti-inflammatory medicines);
- acidic medicines including: salicylates used to treat inflammation (aspirin), sleeping tablets (barbiturates) and lithium (used to treat psychiatric illnesses);
- alkaline (basic) medicines including: sympathomimetics (medicines used in cough & cold preparations (eg. phenylephrine and pseudoephedrine), and for treating ADHD (eg. dexamphetamine).
How Plasma-Lyte 148 and 5% Glucose Replacement Infusion is given
How much it is given
Your doctor will decide how much Plasma-Lyte 148 and 5% Glucose Replacement Infusion will be given to you, which, depends on your need and condition.
You should not be given Plasma-Lyte 56 Maintenance and 5% Glucose Infusion if there are particles floating in the solution or if the pack is damaged in any way.
How it is given
The Plasma-Lyte 148 and 5% Glucose Replacement Infusion will be given at a slow rate of injection (drip) by your health professional. Usually, you will need to stay in a health institution (hospital, nursing home, etc.) but in some cases at home, as it requires a special medical equipment to deliver the medicine into your circulation. This delivery should be attended by a health professional. A cannula (administration needle) is placed in a vein by your doctor or nurse.
The infusion is for single use, and for one person only. Any unused portion must be discarded and not used later, either for you or anyone else.
Your doctor will decide when to stop giving you this infusion.
Ask your doctor or nurse if you want to know more about the use of PlasmaLyte 148 and 5% Glucose Replacement Infusion.
If you are given too much (overdose)
The doctor or nurse giving you the Plasma-Lyte 148 and 5% Glucose Replacement Infusion has had experience in the use of this sort of medicine, so it is unlikely that you will be given an overdose. However, in case of an overdose, the infusion will be discontinued and another treatment may be needed. You may experience some of the effects listed under “Side effects” below.
Tell your doctor, pharmacist or nurse as soon as possible if you do not feel well while you are being given Plasma-Lyte 148 and 5% Glucose Replacement Infusion.
As with any medicine, some side effects may occur.
Tell your doctor immediately if you notice any of the following:
- skin rash;
- shortness of breath (dyspnoea);
- difficulty breathing;
- swelling of the skin of the face, lips and swelling of the throat;
- redness of the skin (erythema).
These are very serious side effects. You may need urgent medical attention.
All of these side effects are very rare.
Other side effects are:
- reactions due to the administration technique:
- fever (febrile response);
- infection at the site of infusion;
- local pain or reaction (redness or swelling) at the site of infusion;
- irritation or inflammation of the vein into which the solution is infused (phlebitis);
- formation of a blood clot (venous thrombosis) at the site of infusion;
- escape of the infusion solution into the tissues around the vein (extravasation);
- an excess of fluid in the body (hypervolaemia);
- high levels of blood potassium which can cause abnormal heart rhythm (hyperkalaemia);
- low blood pressure (hypotension);
- chest discomfort;
- feeling of weakness;
- cold sweat;
Tell your doctor, pharmacist or nurse if you notice anything else that is making you feel unwell.
Other side effects not listed above may occur in some patients.
Discuss any concerns you have with your doctor.
After using Plasma-Lyte 148 and 5% Glucose Replacement Infusion
Plasma-Lyte 148 and 5% Glucose Replacement Infusion will be stored in the pharmacy or the hospital ward. It is recommended that the product be stored below 30°C. Do not freeze.
What it looks like
Plasma-Lyte 148 and 5% Glucose Replacement Infusion is a clear solution filled in plastic bags.
What is in Plasma-Lyte 148 and 5% Glucose Replacement Infusion
The active components are Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, Magnesium Chloride and Glucose-anhydrous.
The other ingredients are water for injections and hydrochloric acid.
Name and address of sponsor
Baxter Healthcare Pty Ltd
1 Baxter Drive
Old Toongabbie NSW 2146
AUST R number
AUST R 19438
Date of preparation: