Patient Leaflet Updated 24-Sep-2018 | Martindale Pharma, an Ethypharm Group Company
Sodium Bicarbonate 8.4% w/v Solution for Injection
Sodium Bicarbonate 8.4% w/v
Solution for Injection
Sodium Bicarbonate
This medicine will be referred to as Sodium Bicarbonate Injection in the rest of this leaflet.
1. What Sodium Bicarbonate Injection is and what it is used for
2. What you need to know before you are given Sodium Bicarbonate Injection
3. How Sodium Bicarbonate Injection is given
4. Possible side effects
5. How to store Sodium Bicarbonate Injection
6. Contents of the pack and other information
Sodium Bicarbonate is one of a group of medicines known as alkalinising agents. It is used to correct the acid-alkaline balance in the body.
Sodium bicarbonate is used to reduce the amount of acid in the body after a heart attack in patients who have the following conditions: too much acid in their body or too much potassium in their blood.
It can also be used to treat patients who have taken too much tricyclic antidepressant medicine. Sodium Bicarbonate will only be used after other resuscitation methods have been attempted.
If any of the above apply to you or your child please tell your doctor or nurse before you are given Sodium Bicarbonate Injection.
Talk to your doctor, pharmacist or nurse before you are given Sodium Bicarbonate Injection.
Your doctor or nurse may want to regularly check your blood acid levels during the course of treatment with this medicine.
Tell your doctor, pharmacist or nurse if you are taking, have recently taken or might take any other medicines.
Including:
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask you doctor or pharmacist for advice before taking this medicine.
This medicinal product contains 23.00 mg sodium per ml, equivalent to 1.15% of the WHO recommended maximum daily intake of 2g sodium for an adult.
This medicine is unlikely to affect your ability to drive or use machines.
Your doctor will give you Sodium Bicarbonate Injection by slow injection into the vein (intravenous injection).
Your doctor will decide on how much Sodium Bicarbonate Injection you should be given.
As this medicine will be given to you whilst you are in hospital, it is unlikely that you will be given too little or too much. Your doctor has information on how to recognise and treat an overdose. If you are concerned about your treatment please talk to your doctor.
Signs of too much sodium bicarbonate include hyperventilation (over breathing), very sensitive to slight stimuli, twitching and high potassium levels in your blood which may cause you to feel dizzy or tired.
Like all medicines, Sodium Bicarbonate Injection can cause side effects, although not everybody gets them.
Side effects 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 Yellow Card Scheme. Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.
Keep all medicines out of the sight and reach of children.
This Sodium Bicarbonate Injection should not be used after the expiry date which is stated on the carton and ampoule label. The doctor or nurse will check that the expiry date on the label has not been passed before administering the injection to you. The expiry date refers to the last day of that month. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment. This product should only be used in a hospital environment and will be safely disposed of by your doctor.
The active substance is Sodium Bicarbonate 8.4%w/v
The other ingredients are disodium edetate, nitrogen and water for injections.
Sodium Bicarbonate Injection is a clear, colourless solution supplied in 5ml and 10ml glass ampoules. Each pack contains 10 ampoules.
If you would like any more information, or would like the leaflet in a different format, please contact Medical Information at the above address
Product licence number: PL 01883/0023
This leaflet was last revised in August 2018
D0422100000
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