Consumer medicine information

Sodium Chloride Injection BP 0.9%

Sodium chloride

BRAND INFORMATION

Brand name

Sodium Chloride Injection BP 0.9% (Fresenius Kabi)

Active ingredient

Sodium chloride

Schedule

Unscheduled

 

Consumer medicine information (CMI) leaflet

Please read this leaflet carefully before you start using Sodium Chloride Injection BP 0.9%.

SUMMARY CMI

Sodium Chloride Injection BP 0.9%

Consumer Medicine Information (CMI) summary

The full CMI on the next page has more details. If you are worried about using this medicine, speak to your doctor or pharmacist.

1. Why am I using Sodium Chloride Injection BP 0.9%?

Sodium chloride Injection BP 0.9% contains the active ingredient sodium chloride. Sodium Chloride 0.9% is used to replace lost body fluids and salts, dilute other medicines, and/or act as a sterile liquid for washing wounds, nasal passages or duri ng surgery.

For more information, see Section 1. Why am I using Sodium Chloride Injection BP 0.9%? in the full CMI.

2. What should I know before I use Sodium Chloride Injection BP 0.9%?

Do not use if you have ever had an allergic reaction to Sodium Chloride Injection BP 0.9% or any of the ingredients listed at the end of the CMI.

Talk to your doctor if you have any other medical conditions, take any other medicines, or are pregnant or plan to become pregnant or are breastfeeding.

For more information, see Section 2. What should I know before I use Sodium Chloride Injection BP 0.9%? in the full CMI.

3. What if I am taking other medicines?

Some medicines may interfere with Sodium Chloride 0.9% and affect how it works.

A list of these medicines is in Section 3. What if I am taking other medicines? in the full CMI.

4. How do I use Sodium Chloride Injection BP 0.9%?

  • Sodium Chloride Injection BP 0.9% will be given to you by your doctor or specially trained nurse.
    They will decide what dose and how long you will receive it for. This depends on your medical condition and other factors.
  • More instructions can be found in Section 4. How do I use Sodium Chloride Injection BP 0.9%? in the full CMI.

5. What should I know while using Sodium Chloride Injection BP 0.9%?

Things you should do
  • If you become pregnant while being given Sodium Chloride Injection BP 0.9% tell your doctor immediately.
  • Remind any doctor, dentist or pharmacist or nurse you visit that you have been given using Sodium Chloride 0.9% Injection.
  • Before surgery, tell the surgeon or anaesthetist that you have been given this medicine.
Driving or using machines
  • Be careful driving or operating machinery until you know how Sodium Chloride 0.9% affects you.
  • If you feel light-headed, dizzy or faint when getting out of bed or a chair, get up slowly.
Looking after your medicine
  • Sodium Chloride Injection BP 0.9% will be stored in the surgery, by your doctor or pharmacist under the recommended conditions of ‘Store below 25°C’.

For more information, see Section 5. What should I know while using Sodium Chloride Injection BP 0.9%? in the full CMI.

6. Are there any side effects?

Sodium Chloride 0.9% may cause nausea, vomiting, diarrhoea, cramps, decrease in saliva, tears or urination, increase in thirst and sweating, increase in heart rate, difficulty breathing or breathlessness which may worsen when lying down, swelling of hands, ankles and feet, dizziness, light headedness, drowsiness, restlessness or irritability, headaches, confusion, muscle weakness, twitching, rigidity or convulsions.

For more information, including what to do if you have any side effects, see Section 6. Are there any side effects? in the full CMI.



FULL CMI

Sodium Chloride Injection BP 0.9%

Active ingredient(s): sodium chloride


Consumer Medicine Information (CMI)

This leaflet provides important information about using Sodium Chloride Injection. You should also speak to your doctor or pharmacist if you would like further information or if you have any concerns or questions about using Sodium Chloride Injection.

Where to find information in this leaflet:

1. Why am I using Sodium Chloride Injection?
2. What should I know before I use Sodium Chloride Injection?
3. What if I am taking other medicines?
4. How do I use Sodium Chloride Injection?
5. What should I know while using Sodium Chloride Injection?
6. Are there any side effects?
7. Product details

1. Why am I using Sodium Chloride Injection?

Sodium Chloride Injection contains the active ingredient Sodium Chloride.

Sodium Chloride Injection is used to:

  • replace lost body fluids and salts.
  • dilute other medicines, which may be given by injection or drip
  • act as a sterile liquid for washing wounds, nasal passages or during surgery

Your doctor may have prescribed it for another reason.

Ask your doctor if you have any questions about why this medicine has been prescribed for you.

2. What should I know before I use Sodium Chloride Injection?

Warnings

Your doctor will have considered the need to give you Sodium Chloride 0.9% carefully. Make sure to tell the doctor if you have any allergies.

Do not use Sodium Chloride Injection if you are allergic to

  • Sodium chloride
  • Any other medicines
  • Any other substance such as food dyes, preservatives or plastics
  • Any of the ingredients listed at the end of this leaflet.

Some of the symptoms of an allergic reaction may include:

  • shortness of breath
  • wheezing or difficulty breathing
  • swelling of the face, lips, tongue, or other parts of the body
  • rash, itching or hives on the skin.
  • Always check the ingredients to make sure you can use this medicine.

Check with your doctor if you:

  • have any other medical conditions such as:
    - Heart problems
    - Severe kidney disease
    - Breathlessness which may be severe or worsen when lying down
    - Excess fluid in the lungs
    - Swelling due to excess fluid
    - Kidney disease
    - High blood pressure including high blood pressure due to pregnancy
    - Problems with urinary tract

During treatment, you may be at risk of developing certain side effects. It is important you understand these risks and how to monitor for them. See additional information under Section 6. Are there any side effects?

Pregnancy and breastfeeding

Check with your doctor if you are pregnant or intend to become pregnant.

Talk to your doctor if you are breastfeeding or intend to breastfeed.

Unless specifically prescribed by your doctor, you should not be given Sodium Chloride 0.9% if you are pregnant or breast feeding. Ask your doctor about the risks and benefits involved.

Use in Children

  • Sodium Chloride 0.9% should be administered with care to very young patients.

Use in Elderly

  • Sodium Chloride 0.9% should be administered with care to elderly patients

3. What if I am taking other medicines?

Tell your doctor or pharmacist if you are taking any other medicines, including any medicines, vitamins or supplements that you buy without a prescription from your pharmacy, supermarket or health food shop.

Some medicines may interfere with Sodium Chloride 0.9% and affect how it works.

These include:

  • Corticosteroids
  • Corticotrophin
  • Other drugs that cause sodium to be retained in the body.

Check with your doctor or pharmacist if you are not sure about what medicines, vitamins or supplements you are taking and if these affect Sodium Chloride Injection.

4. How do I use Sodium Chloride Injection?

How much to use

  • Your doctor will decide what dose, how often and how long you will receive it. This depends on your condition and other factors, such as your weight, age, blood tests, how well your kidneys are working, and whether or not other medicines are being given at the same time.

How to use Sodium Chloride 0.9%

Sodium Chloride 0.9% Injection will be given to you by your doctor or specially trained nurse.

If you are given too much Sodium Chloride Injection

This rarely happens as Sodium Chloride Injection is administered under the care of a trained professional in a hospital or clinic setting.

However, the first signs of an overdose can be nausea, vomiting, diarrhoea, cramps, reduced saliva, increased thirst and sweating.

You should immediately:

  • phone the Poisons Information Centre
    (by calling 13 11 26), or
  • contact your doctor, or
  • go to the Emergency Department at your nearest hospital.

You should do this even if there are no signs of discomfort or poisoning.

5. What should I know while using Sodium Chloride Injection?

Things you should do

If you are about to be started on any new medicine, remind your doctor and pharmacist that you have been given Sodium Chloride 0.9%.

Tell any other doctors, dentists, and pharmacists who treat you that you have been given Sodium Chloride 0.9%.

If you are going to have surgery, tell the surgeon or anaesthetist that you have been given Sodium Chloride 0.9%. It may affect other medicines used during the surgery.

If you feel lightheaded or faint when getting out of bed or standing up, get up slowly.

Standing up slowly, especially when you get up from a bed or a chair, will help your body get used to the change in position and blood pressure. If this problem continues to get worse talk to your doctor

Call your doctor straight away if you:

  • become pregnant during the course of Sodium Chloride 0.9% treatment.

Remind any doctor, dentist, pharmacist or nurse you visit that you have been given Sodium Chloride 0.9%.

Driving or using machines:

Be careful before you drive or use any machines or tools until you know how Sodium Chloride 0.9% affects you.

Sodium Chloride 0.9% may cause dizziness, lightheadedness, drowsiness, or weakness in some people. If you have any of these symptoms, do not drive, operate machinery, or do anything else dangerous.

Looking after your medicine

  • Sodium Chloride Injection 0.9% will be stored in the surgery, pharmacy or ward of a hospital. The medicine is kept in a cool dry place where the temperature stays below 25°C.
  • Sodium Chloride Injection 0.9% will only be opened when it is time for you to have the injection.
  • It should not be stored after it is opened nor used for more than one person

Keep it where young children cannot reach it.

Getting rid of any unwanted medicine

Any Sodium Chloride 0.9% Injection which is not used and which is left in the container, will be disposed of in a safe manner by your doctor or pharmacist.

6. Are there any side effects?

All medicines can have side effects. The use of Sodium Chloride 0.9% to replace lost body fluids and salts or addition to intravenous fluids is unlikely to result in any side effects. If you do experience any side effects, most of them are minor and temporary. However, some side effects may need medical attention.

See the information below and, if you need to, ask your doctor or pharmacist if you have any further questions about side effects.

Less serious side effects

Less serious side effectsWhat to do
A decrease in saliva, tears or urination and/or an increase in thirst and sweating may be experienced.
Other side effects may include:
Nervous system:
  • headaches, confusion
Musculoskeletal:
  • cramps
Speak to your doctor if you have any of these less serious side effects and they worry you.

Serious side effects

Serious side effectsWhat to do
Swelling of hands, ankles and feet may be experienced.
Other side effects may include:
Cardiovascular:
  • increase in heart rate
Gastrointestinal:
  • nausea, vomiting, diarrhoea
Respiratory:
  • difficulty breathing or breathlessness which may worsen when lying down
Musculoskeletal:
  • muscle weakness, twitching, rigidity, or convulsions
Nervous system:
  • dizziness, light headedness, drowsiness, restlessness, or irritability
Call your doctor straight away or go straight to the Emergency Department at your nearest hospital if you notice any of these serious side effects.

Tell your doctor or pharmacist if you notice anything else that may be making you feel unwell.

Other side effects not listed here may occur in some people.

If you are over 65 years of age or very young, you may have an increased chance of getting side effects

Reporting side effects

After you have received medical advice for any side effects you experience, you can report side effects to the Therapeutic Goods Administration online at www.tga.gov.au/reporting-problems. By reporting side effects, you can help provide more information on the safety of this medicine.

Always make sure you speak to your doctor or pharmacist before you decide to stop taking any of your medicines.

7. Product details

This medicine is only available with a doctor's prescription.

What Sodium Chloride Injection contains

Active ingredient
(main ingredient)
Sodium Chloride
Other ingredients
(inactive ingredients)
Water for Injections
Potential allergensNone

Do not take this medicine if you are allergic to any of these ingredients.

What Sodium Chloride Injection looks like

Sodium Chloride Injection is a clear, colourless solution supplied in ampoules in the following strengths:

5 mL AUST R 197200

10 mL AUST R 197198

20 mL AUST R 197199

Who distributes Sodium Chloride Injection

Fresenius Kabi Australia Pty Limited
Level 2, 2 Woodland Way
Mount Kuring-gai NSW 2080
Australia
Telephone: (61-2) 9391 5555

Fresenius Kabi New Zealand Limited
c/o GNZCC, HSBC Tower, Level 14, 188 Quay Street,
Auckland
New Zealand
Freecall: 0800 144 892

This leaflet was prepared in November 2021

Published by MIMS February 2022

BRAND INFORMATION

Brand name

Sodium Chloride Injection BP 0.9% (Fresenius Kabi)

Active ingredient

Sodium chloride

Schedule

Unscheduled

 

1 Name of Medicine

Sodium chloride.

2 Qualitative and Quantitative Composition

Sodium Chloride Injection BP 0.9% contains sodium chloride 0.9% (9 mg/mL) in Water for Injections.
For the full list of excipients, see Section 6.1 List of Excipients.

3 Pharmaceutical Form

Solution for Injection.
Sodium Chloride Injection BP 0.9% is a sterile, preservative-free solution, pH 4.5-7.0.

4 Clinical Particulars

4.1 Therapeutic Indications

Sodium Chloride Injection BP 0.9% can be used as the vehicle for many parenteral drugs and as an electrolyte replenisher for maintenance or replacement of deficits of extracellular fluid. It can also be used as a sterile irrigation medium.

4.2 Dose and Method of Administration

To be used as directed by a physician.
Parenteral drug products should be inspected prior to administration for particulate matter and discolouration. Sodium Chloride Injection BP 0.9% does not contain any antimicrobial preservatives. Care should be taken with intravenous technique to avoid injection site reactions and infections.
Dosage is dependent on the age, weight, clinical and fluid/ electrolyte condition of the patient.

4.3 Contraindications

Congestive heart failure.
Severe renal impairment.
Conditions of sodium retention and oedema.
Liver cirrhosis.
Irrigation during electrosurgical procedures.

4.4 Special Warnings and Precautions for Use

Solutions containing sodium chloride should be used cautiously in patients with cardiovascular diseases such as congestive heart failure, hypertension, impaired renal function or other renal diseases such as urinary tract obstruction, pregnancy associated hypertension, pulmonary or peripheral oedema, hypoproteinaemia, those receiving corticosteroids or corticotrophin or any condition associated with sodium retention.
Sodium chloride solutions should be used with caution in geriatric patients and infants.
Excessive administration of sodium chloride solution may result in resulting in hypernatraemia, dehydration of internal organs, hypokalaemia and acidosis. Monitoring of fluid, electrolyte and acid-base balance may be necessary.
When used as a vehicle for intravenous drug delivery, the Product Information document of such drugs should be checked prior to use to ensure compatibility with the sodium chloride solution. Reconstitution instructions should be read carefully.
Do not use unless the solution is clear. The entire contents of the ampoule should be used promptly.
Intravenous infusion during or immediately after surgery may result in sodium retention.

Use in the elderly.

No data available.

Paediatric use.

No data available.

Effects on laboratory tests.

No data available.

4.5 Interactions with Other Medicines and Other Forms of Interactions

Additives may be incompatible with sodium chloride.
Do not store solutions containing additives unless compatibility has been proven.
Do not administer such preparations unless the solution is clear.
Comedication of drugs inducing sodium retention may exacerbate any systemic effects.

4.6 Fertility, Pregnancy and Lactation

Effects on fertility.

No data available.
Safety in pregnancy has not been established. Use is recommended only when clearly indicated.
Safety in lactation has not yet been established. Use of this product whilst breastfeeding is recommended only when potential benefits outweigh potential risks to the newborn.

4.7 Effects on Ability to Drive and Use Machines

The effects of this medicine on a person's ability to drive and use machines were not assessed as part of its registration.
However, adverse effects of these medicines include dizziness, which could affect the ability to drive or use machines (see Section 4.8 Adverse Effects (Undesirable Effects)).

4.8 Adverse Effects (Undesirable Effects)

Thrombophlebitis may occur at the injection site during prolonged infusions.
Excess intravenous administration of sodium chloride may cause hypernatraemia, hypokalaemia and acidosis.
Hypernatraemia rarely occurs with therapeutic doses of sodium chloride, but may occur in excessive administration. A serious complication of this is dehydration of the brain causing somnolence and confusion, which may progress to convulsions, coma and ultimately respiratory failure and death. Other symptoms include thirst, reduced salivation and lachrymation, fever, tachycardia, hypertension, headache, dizziness, restlessness, weakness and irritability.

Reporting of suspected adverse effects.

Reporting suspected adverse reactions after registration of the medicinal product is important. It allows continued monitoring of the benefit-risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions at www.tga.gov.au/reporting-problems.

4.9 Overdose

Symptoms of over dosage.

Excess sodium chloride within the body may produce the following general gastrointestinal effects: nausea, vomiting, diarrhoea and cramps.
Salivation and lacrimation are reduced, whilst thirst and swelling are increased.
Possible other symptoms include hypotension, tachycardia, renal failure, peripheral and pulmonary oedema and respiratory arrest.
Symptoms of the CNS include headache, dizziness, irritability, restlessness, weakness, muscle twitching or rigidity, convulsions, coma and death.

Treatment of over dosage.

Normal plasma sodium concentrations should be restored at no more than 10-15 mmol/day with IV hypotonic saline. Dialysis may be required if there is renal impairment, if plasma sodium levels are greater than 200 mmol/L or if the patient is moribund. Convulsions should be treated with diazepam.
For information on the management of overdose, contact the Poison Information Centre on 131126 (Australia).

5 Pharmacological Properties

5.1 Pharmacodynamic Properties

Mechanism of action.

Sodium Chloride Injection BP 0.9% provides a source of sodium ions (154 mmol/L), chloride ions (154 mmol/L) and water. With an osmolarity of approx. 308 mOsmol/L, the product is isotonic, and therefore designated as physiological sodium chloride solution.
Sodium is the major cation of extracellular fluid and functions principally in the control of water distribution, fluid and electrolyte balance and osmotic pressure of body fluids. Chloride, the major extracellular anion, closely follows the physiological disposition of the sodium cation in maintenance of acid base balance, isotonicity and electrodynamic characteristics of cells.

Clinical trials.

No data available.

5.2 Pharmacokinetic Properties

As sodium chloride intravenous preparations are directly administered to the circulation, the bioavailability of the components is 100%.

Excretion.

Excess sodium is predominantly excreted by the kidneys, with small amounts lost in faeces and sweat.

5.3 Preclinical Safety Data

Genotoxicity.

The active ingredients sodium and chloride are not mutagenic. They are basic cellular components.

Carcinogenicity.

The active ingredients sodium and chloride are not carcinogenic. They are basic cellular components.

6 Pharmaceutical Particulars

6.1 List of Excipients

Water for injections as well as hydrochloric acid and sodium hydroxide for pH adjustment.

6.2 Incompatibilities

Additives may be incompatible with sodium chloride.

6.3 Shelf Life

In Australia, information on the shelf life can be found on the public summary of the Australian Register of Therapeutic Goods (ARTG). The expiry date can be found on the packaging.

6.4 Special Precautions for Storage

Store below 25°C.

6.5 Nature and Contents of Container

AUST R 197200 Sodium Chloride Injection BP 0.9% 5 mL ampoule (20's).
AUST R 197198 Sodium Chloride Injection BP 0.9% 10 mL ampoule (20's, 50's).
AUST R 197199 Sodium Chloride Injection BP 0.9% 20 mL ampoule (20's).
Sodium Chloride Injection BP 0.9% are available in LDPE and PP ampoules.
* Not all pack sizes/volumes may be marketed.

6.6 Special Precautions for Disposal

In Australia, any unused medicine or waste material should be disposed of in accordance with local requirements.

6.7 Physicochemical Properties

Chemical structure.

Molecular formula: NaCl.
Molecular weight: 58.44.
Sodium chloride is a white, crystalline powder or colourless crystals, freely soluble in water and practically insoluble in ethanol.

CAS number.

7647-14-5.

7 Medicine Schedule (Poisons Standard)

Australia: Unscheduled.

Summary Table of Changes