Patient Leaflet Updated 06-Feb-2025 | hameln pharma ltd
Lidocaine Hydrochloride Injection BP 2% w/v
Lidocaine Hydrochloride Injection 2%
Lidocaine Hydrochloride
1. What Lidocaine Hydrochloride Injection 2% is and what it is used for
2. What you need to know before you use Lidocaine Hydrochloride Injection 2%
3. How to use Lidocaine Hydrochloride Injection 2%
4. Possible side effects
5. How to store Lidocaine Hydrochloride Injection 2%
6. Contents of the pack and other information
Lidocaine Hydrochloride Injection 2% is a local anaesthetic. It is used to:
The preparation of this particular medicine (i.e. hameln Lidocaine Hydrochloride Injection 2%) makes it unsuitable for use in the eye – therefore this medicine MUST NOT be used in the eye.
Talk to your doctor, pharmacist or nurse before using Lidocaine Hydrochloride Injection 2%:
Tell your doctor, pharmacist or nurse if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription. This is especially important with the following medicines as they may interact with your Lidocaine Hydrochloride Injection 2%:
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Depending on where and how lidocaine hydrochloride is used, it may affect your ability to drive or operate machinery. Ask your doctor about when it would be safe to drive or operate machines.
You should not drive or use machinery if you are affected by the administration of Lidocaine Hydrochloride Injection 2%.
This medicine (i.e. hameln Lidocaine Hydrochloride Injection 2%) MUST NOT be used in the eye.
Your nurse or doctor will give you the injection.
Your doctor will decide the correct dosage for you and how and when the injection will be given.
Since the injection will be given to you by a doctor or nurse, it is unlikely that you will be given too much.
If you think you have been given too much, or you begin to experience lightheadedness, numbness of your tongue or a ringing in your ears you must tell the person giving you the injection immediately.
Like all medicines, Lidocaine Hydrochloride Injection 2% can cause side effects, although not everybody gets them.
Nervous and psychiatric disorders:
Eye disorders:
Ear disorders:
Heart disorders:
Breathing disorders:
Gastrointestinal disorders:
Skin disorders:
Blood disorders
After spinal injection of lidocaine, you should tell your doctor if you experience any of the following side effects:
For patients going home before the numbness or loss of feeling caused by a local anaesthetic wears off:
If you think this injection is causing you any problems, or you are at all worried, talk to your doctor, nurse or pharmacist.
If you get any side effects, talk to your doctor, pharmacist or nurse: This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: 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 this medicine out of the sight and reach of children.
Your injection will be stored at less than 25°C and protected from light.
Do not use this medicine after the expiry date which is stated on the label and carton. The expiry date refers to the last day of that month.
The active substance is lidocaine hydrochloride. In Lidocaine Hydrochloride Injection 2% each ml of solution contains 20 mg of lidocaine hydrochloride in a sterile solution for injection.
The other ingredients are hydrochloric acid, sodium hydroxide and water for injections.
Lidocaine Hydrochloride Injection 2% is a clear, colourless, solution for injection in a clear glass ampoule containing 2, 5, 10 or 20 ml. Not all ampoule sizes may be marketed.
The marketing authorisation number of this medicine is: PL 01502/0021R.
For any information about this medicine, please contact the Marketing Authorisation Holder
This leaflet was revised in July 2024.
6625/36/24
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