Patient Leaflet Updated 03-Jun-2025 | Baxter Healthcare Ltd
Sodium Chloride 0.45% Solution for Infusion
Sodium Chloride 0.45 % Solution for Infusion
Active substance: sodium chloride
This medicine is called `Sodium Chloride 0.45% Solution for Infusion’, but will be referred to as `Sodium 0.45 Infusion’ throughout the remainder of this leaflet.
1. What Sodium 0.45 Infusion is and what it is used for
2. What you need to know before you are given Sodium 0.45 Infusion
3. How you will be given Sodium 0.45 Infusion
4. Possible side effects
5. How to store Sodium 0.45 Infusion
6. Contents of the pack and other information
Sodium 0.45 Infusion is a solution of sodium chloride in water. Sodium chloride is a chemical substance (often called “salt”) found in the blood.
Sodium 0.45 Infusion is used to treat:
Sodium 0.45 infusion may also be used to deliver or to dilute other medicines for infusion.
If a medicine has been added to Sodium 0.45 Infusion, the Package Leaflet of the added medicine must be consulted to determine whether or not you can receive the solution.
Please tell your doctor if you have or have had any of the following medical conditions:
This may increase the risk of low levels of sodium in your blood and can lead to headache, nausea, seizures, lethargy, coma, swelling of the brain and death. Brain swelling increases the risk of death and brain damage. People who are at higher risk of brain swelling are:
Some patients are at higher risk for having or developing a too low sodium concentration in your blood (hyponatraemia). In general this applies to:
Please 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:
You should ask your doctor about what you can eat or drink.
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.
If another medicine is to be added to your solution for infusion during pregnancy or breast-feeding you should:
Ask your doctor or nurse for advice before driving or using machines.
Sodium 0.45 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, the reason for treatment and whether or not the infusion is being used to deliver or dilute another medicine.
The amount you are given may also be affected by other treatments you are receiving.
You should NOT be given Sodium 0.45 Infusion if there are particles floating in the solution or if the pack is damaged in any way.
Sodium 0.45 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:
This is especially important for children as they have a limited ability to regulate fluids and electrolytes.
Any unused solution should be thrown away. You should NOT be given an infusion of Sodium 0.45 Infusion from a bag that has been partly used.
If you are given too much Sodium 0.45 Infusion (over-infusion), or it is given too fast, this may lead to the following symptoms:
If Sodium 0.45 Infusion is given too fast when you have higher than normal levels of salts in the blood (hypertonicity), swelling of the brain (brain oedema) is possible, especially if you often have higher than normal levels of sodium in the blood (hypernatraemia).
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 Sodium 0.45 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 medicine, ask your doctor or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The side effects that may occur due to the administration technique include:
Other side effects noted with similar products (sodium chloride containing solutions) include:
If a medicine has been added to the solution for infusion, the added medicine may also cause side effects.
These side effects will depend on the medicine that has been added. You should read the Package Leaflet of the added medicine for a list of possible symptoms.
If you get any side effect, talk to your doctor or nurse. This includes any possible side effect not listed in this leaflet. You can also report side effects directly via the national reporting system listed below. By reporting side effects, you can help provide more information on the safety of this medicine.
United Kingdom:
Via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard
Ireland
If any side effects occur, the infusion must be stopped.
Keep this medicine out of the sight and reach of children.
Sodium 0.45 Infusion does not require special storage conditions.
Sodium 0.45 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 Sodium 0.45 Infusion, if there are particles floating in the solution or if the unit is damaged in any way.
The active substance is sodium chloride: 4,5 g per litre.
The only other ingredient is water for injections
Sodium Chloride 0.45% Solution for 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 size is 500 ml
The bags are supplied in cartons. Each carton contains 20 bags of 500 ml
Marketing Authorisation Holder for the United Kingdom:
Marketing Authorisation Holder for Ireland:
Manufacturers for Great Britain:
Manufacturers for Ireland:
This medicinal product is authorised in the Member States of the EEA under the following names:
Ireland, UK: Sodium Chloride 0.45 % Solution for Infusion
Finland: Natriumklorid Baxter Viaflo 4,5 mg/ml infuusioneste, liuos
This leaflet was last approved in September 2024
For information about Sodium Chloride 0.45% 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-30-02-250
Caxton Way, Thetford, Norfolk, IP24 3SE, UK
0800 0260516
https://medinfo.baxterhealthcare.co.uk
https://www.baxterhealthcare.co.uk/
0800 028 9881