• Keep this leaflet. You may need to read it again.
• If you have further questions, ask your anaesthetist or doctor.
• If you get any side effects, talk to your anaesthetist or other doctor. This includes any possible side effects not listed in this leaflet. See section 4.

1. What Bridion is and what it is used for
2. What you need to know before Bridion is given
3. How Bridion is given
4. Possible side effects
5. How to store Bridion
6. Contents of the pack and other information

Bridion contains the active substance sugammadex. Bridion is considered to be a Selective Relaxant Binding Agent since it only works with specific muscle relaxants, rocuronium bromide or vecuronium bromide.

When you have some types of operations, your muscles must be completely relaxed. This makes it easier for the surgeon to do the operation. For this, the general anaesthetic you are given includes medicines to make your muscles relax. These are called muscle relaxants, and examples include rocuronium bromide and vecuronium bromide. Because these medicines also make your breathing muscles relax, you need help to breathe (artificial ventilation) during and after your operation until you can breathe on your own again.

Bridion is used to speed up the recovery of your muscles after an operation to allow you to breathe on your own again earlier. It does this by combining with the rocuronium bromide or vecuronium bromide in your body. It can be used in adults whenever rocuronium bromide or vecuronium bromide is used and in children and adolescents (aged 2 to 17 years) when rocuronium bromide is used for a moderate level of relaxation.

• if you are allergic to sugammadex or any of the other ingredients of this medicine (listed in section 6).

• Tell your anaesthetist if this applies to you.

Talk to your anaesthetist before Bridion is given

• if you have kidney disease or had in the past. This is important as Bridion is removed from your body by the kidneys.
• if you have liver disease or have had it in the past.
• if you have fluid retention (oedema).
• if you have diseases which are known to give an increased risk of bleeding (disturbances of blood clotting) or anticoagulation medication.

This medicine is not recommended for infants less than 2 years of age.

• Tell your anaesthetist if you are taking, have recently taken or might take any other medicines.

Bridion may affect other medicines or be affected by them.

Some medicines reduce the effect of Bridion

• It is especially important that you tell your anaesthetist if you have recently taken:

• toremifene (used to treat breast cancer).
• fusidic acid (an antibiotic).

Bridion can affect hormonal contraceptives

• Bridion can make hormonal contraceptives - including the ‘Pill’, vaginal ring, implants or a hormonal IntraUterine System (IUS) - less effective because it reduces how much you get of the progestogen hormone. The amount of progestogen lost by using Bridion is about the same as missing one oral contraceptive Pill.
  - If you are taking the Pill on the same day as Bridion is given to you, follow the instructions for a missed dose in the Pill’s package leaflet.
  - If you are using other hormonal contraceptives (for example a vaginal ring, implant or IUS) you should use an additional non-hormonal contraceptive method (such as a condom) for the next 7 days and follow the advice in the package leaflet.

In general, Bridion does not have an effect on laboratory tests. However, it may affect the results of a blood test for a hormone called progesterone. Talk to your doctor if your progesterone levels need to be tested on the same day you receive Bridion.

• Tell your anaesthetist if you are pregnant or might be pregnant or if you are breast-feeding.

You may still be given Bridion, but you need to discuss it first.

It is not known whether sugammadex can pass into breast milk. Your anaesthetist will help you decide whether to stop breast-feeding, or whether to abstain from sugammadex therapy, considering the benefit of breast-feeding to the baby and the benefit of Bridion to the mother.

Bridion has no known influence on your ability to drive and use machines.

This medicine contains up to 9.7 mg sodium (main component of cooking / table salt) in each mL.

This is equivalent to 0.5 % of the recommended maximum daily dietary intake of sodium for an adult.

Your anaesthetist will work out the dose of Bridion you need based on:

• your weight
• how much the muscle relaxant medicine is still affecting you.

The usual dose is 2-4 mg per kg body weight for adults and for children and adolescents between 2-17 years old. A dose of 16 mg/kg can be used in adults if urgent recovery from muscle relaxation is needed.

Bridion will be given to you by your anaesthetist. It is given as a single injection through an intravenous line.

As your anaesthetist will be monitoring your condition carefully, it is unlikely that you will be given too much Bridion. But even if this happens, it is unlikely to cause any problems.

If you get any side effects, talk to your anaesthetist or other doctor. 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.

• The active substance is sugammadex.
  1 mL solution for injection contains sugammadex sodium equivalent to 100 mg sugammadex.
  Each vial of 2 mL contains sugammadex sodium equivalent to 200 mg sugammadex.
  Each vial of 5 mL contains sugammadex sodium equivalent to 500 mg sugammadex.
• The other ingredients are water for injections, hydrochloric acid 3.7% and/or sodium hydroxide.

Bridion is a clear and colourless to slightly yellow solution for injection.

It comes in two different pack sizes, containing either 10 vials with 2 mL or 10 vials with 5 mL solution for injection.

Not all pack sizes may be marketed.

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Manufacturer:

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