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The product code(s) for this leaflet is: PL 00116/0334.
Sodium Chloride 0.9% Intravenous Infusion BP
Sodium Chloride 0.9% w/v Intravenous Infusion BP
Active substance: sodium chloride
This medicine is called ‘Sodium Chloride 0.9% w/v Intravenous Infusion BP’, but will be referred to as ‘Sodium 0.9 Infusion’ throughout the remainder of this leaflet.
1. What Sodium 0.9 Infusion is and what it is used for
2. What you need to know before you are given Sodium 0.9 Infusion
3. How you will be given Sodium 0.9 Infusion
4. Possible side effects
5. How to store Sodium 0.9 Infusion
6. Contents of the pack and other information
Sodium 0.9 Infusion is a solution of sodium chloride in water. Sodium chloride is a chemical substance (often called “salt”) found in the blood.
Sodium 0.9 Infusion is used to treat:
Situations that may cause sodium chloride and water loss include:
Sodium 0.9 Infusion may also be used to deliver or to dilute other medicines for infusion.
If a medicine has been added to Sodium 0.9 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:
When you are given this infusion, your doctor will take blood and urine samples to monitor:
This is especially important for children and (premature) babies as they can retain too much sodium due to their immature kidney function.
Your doctor will take into account if you are receiving parenteral nutrition (nutrition given by infusion into a vein). During long term treatment with Sodium 0.9 Infusion you may need to be given extra nutrition.
Tell your doctor or nurse if you are using, have recently used or might use any other medicines.
It is particularly important that you inform your doctor if you are taking:
These medicines can cause the body to accumulate sodium and water, leading to tissue swelling due to fluid collection under the skin (oedema) and high blood pressure (hypertension).
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.
However, 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 0.9 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 0.9 Infusion if there are particles floating in the solution or if the pack is damaged in any way.
Sodium 0.9 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:
the amount of electrolytes in your body (particularly sodium, in patients with high levels of the hormone vasopressin, or are taking other medicines which increase the effects of vasopressin).
Any unused solution should be thrown away. You should NOT be given an infusion of Sodium 0.9 Infusion from a bag that has been partly used.
If you are given too much Sodium 0.9 Infusion (over-infusion), 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 Sodium 0.9 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 or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them. The frequency of the side-effects is unknown.
Low levels of sodium in the blood that may be acquired during hospitalization (nosocomial hyponatraemia) and related neurological disorder (acute hyponatraemic encephalopathy). Hyponatraemia can lead to irreversible brain injury and death due to (cerebral oedema/swelling) (see also in the section 2 “Warning and precautions”).
Side effects that may occur due to the administration technique include:
Other side effects noted with similar products (other sodium containing solutions) include:
If you get any side effects, talk to your doctor or pharmacist or nurse. This includes any possible side effects 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:
Malta
If any side effects occur, the infusion must be stopped.
Keep this medicine out of the sight and reach of children.
50 ml and 100 ml bags: do not store above 30°C. 250 ml, 500 ml and 1000 ml bags: this medicine does not require any special storage conditions.
You should NOT be given this medicine 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 this medicine if there are particles floating in the solution or if the unit is damaged in any way.
The active substance is sodium chloride: 9 g per litre
The only other ingredient is water for injections
Sodium 0.9 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:
Pack sizes:
Not all pack sizes may be marketed
Marketing Authorisation Holder:
United Kingdom
Ireland and Malta
Manufacturers for Great Britain:
Manufacturers for Ireland and Malta:
This leaflet was last revised in June 2023
For information about Sodium Chloride 0.9% 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-30-02-187