Find similar products:
The text only version may be available in large print, Braille or audio CD. For further information call emc accessibility on 0800 198 5000. The product code(s) for this leaflet is: PL 12064/0038.
Midazolam 1mg/ml Injection
Midazolam 1mg/ml Injection
Midazolam Hydrochloride
1. What Midazolam Injection is and what it is used for
2. What you need to know before you are given Midazolam Injection
3. How Midazolam Injection will be given
4. Possible side effects
5. How to store Midazolam Injection
6. Contents of the pack and other information
Midazolam belongs to a group of medicines known as benzodiazepines. It is a short-acting medicine that is used to induce sedation (a very relaxed state of calm, drowsiness or sleep) and relieves anxiety and muscle tension.
This medicine is used for:
You must not be given Midazolam Injection if any of the above apply to you. If you are not sure, talk to your doctor or nurse before you are given this medicine.
Children and babies
If your child is going to be given this medicine:
Adults
Before Midazolam Injection is given, let your doctor or nurse know if:
If any of the above apply to you, or if you are not sure, talk to your doctor or nurse before you are given Midazolam Injection.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription and herbal medicines.
This is extremely important, as using more than one medicine at the same time can strengthen or weaken the effect of the medicines involved. In particular, tell your doctor or nurse if you are taking any of the following medicines:
If any of the above apply to you, or if you are not sure, talk to your doctor or nurse before you are given Midazolam Injection.
Concomitant use of Midazolam Injection and opioids (strong pain killers, medicines for substitution therapy and some cough medicines) increases the risk of drowsiness, difficulties in breathing (respiratory depression), coma and may be life-threatening. Because of this, concomitant use should only be considered when other treatment options are not possible.
However, if your doctor does prescribe Midazolam Injection together with opioids the dose and duration of concomitant treatment should be limited by your doctor. Please tell your doctor about all opioid medicines you are taking, and follow your doctor's dose recommendation closely. It could be helpful to inform friends or relatives to be aware of the signs and symptoms stated above. Contact your doctor when experiencing such symptoms.
If you are going to have an inhaled anaesthetic (one that you breathe in) for an operation or for dental treatment, it is important to tell your doctor or dentist that you have been given Midazolam Injection.
Do not drink alcohol if you have been given Midazolam Injection. This is because alcohol can increase the sedative effect of Midazolam Injection and may cause problems with your breathing.
Tell your doctor if you are pregnant, think you may be pregnant or are planning to have a baby. Your doctor will decide if this medicine is suitable for you
Midazolam Injection may harm your unborn baby when used in early pregnancy. When high doses are administered during late pregnancy, labour or caesarean section, you might have an inhalation risk and your baby might have an irregular heartbeat, state of low muscle tone (hypotonia), feeding difficulties, a low body temperature and difficulty in breathing. With prolonged administration during late pregnancy, your baby may develop a physical dependence and risk of withdrawal symptoms after birth.
Do not breast-feed for 24 hours after being given Midazolam Injection. This is because Midazolam Injection may pass into your breast milk.
This medicine can affect your ability to drive and operate machinery as it may make you sleepy or dizzy.
Talk to your doctor or pharmacist if you are not sure whether it is safe for you to drive while taking this medicine.
This medicine contains 3.46 mg sodium (main component of cooking/table salt) in each ml. This is equivalent to 0.17% of the recommended maximum daily dietary intake of sodium for an adult.
Talk to your pharmacist or doctor if you need Midazolam Injection on a daily basis for a prolonged period of time, especially if you have been advised to have a low salt diet.
Midazolam Injection should be given only by experienced healthcare professionals (doctor or nurse). It should be given in a place (hospital, clinic or surgery) equipped to monitor and support the patient's breathing, heart and circulation (cardiovascular function) and recognise the signs of and manage the expected side effects of anaesthesia.
Your doctor will decide on a suitable dose for you. The dose you are given will depend on why you are being treated and the type of sedation needed. Your weight, age, your state of health, how you respond to Midazolam Injection and whether other medicines are needed at the same time will also influence the dose that you are given.
If you need strong painkillers, you will be given these first and then be given Midazolam Injection. The dose will be adjusted specially for you.
You should always be taken home by a responsible adult after your treatment.
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, however, tell your doctor or nurse if you have any concerns.
If you are accidentally given too much Midazolam Injection you may:
If you receive long term treatment with Midazolam Injection (are given the medicine for a long time) you may:
Your doctor will reduce your dose gradually to avoid these effects happening to you.
Benzodiazepine medicines, like Midazolam Injection, may make you dependent if used for a long time (for instance in intensive care). This means that if you stop treatment suddenly, or lower the dose too quickly, you may get withdrawal symptoms. The symptoms can include:
If you have any further questions on the use of this medicine, ask your doctor or nurse.
Like all medicines, Midazolam Injection can cause side effects, although not everybody gets them.
The following undesirable effects have been reported (frequency not known).
Life-threatening side effects are more likely to occur in adults over 60 years of age and those who already have breathing difficulties or heart problems, particularly if the injection is given too fast or at a high dose
Not known: frequency cannot be estimated from the available data
If you get any side effects, talk to your doctor 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 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.
Your doctor or pharmacist is responsible for storing Midazolam Injection . They are also responsible for disposing of any unused Midazolam Injection correctly.
Keep out of the sight and reach of children.
You should not be given Midazolam Injection after the expiry date which is printed on the carton and vial label. The doctor, nurse or anaesthetist 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.
Do not store above 25°C. Keep the container in the outer carton in order to protect from light.
The active substance is Midazolam Hydrochloride 50mg in 50ml.
The other ingredients are hydrochloric acid 10%, sodium chloride, sodium hydroxide and water for injections
Midazolam Injection is a clear, colourless solution supplied in a clear glass vial containing 50ml of the solution.
This leaflet was last revised in August 2023.
Product Licence Number: PL 12064/0038
D06046