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Package Leaflet: Information for the User
Sugammadex Normon 100 mg/ml Solution for Injection EFG
Read all of this leaflet carefully before you are given this medicine because it contains important information for you.
Contents of the Package Leaflet
What is Sugammadex Normon
This medicine contains the active substance sugammadex. Sugammadex is considered a Selective Relaxant Binding Agent as it only works with specific muscle relaxants, rocuronium bromide or vecuronium bromide.
What Sugammadex Normon is used for
If you have to undergo surgery, your muscles must be completely relaxed, making it easier for the surgeon to perform the operation. For this, during general anesthesia, you will be given medications to relax your muscles. These are called muscle relaxants, such as rocuronium bromide and vecuronium bromide. Since these medications also block the respiratory muscles, you will need help breathing (artificial respiration) during and after surgery until you can breathe on your own again.
Sugammadex Normon is used to speed up the recovery of your muscles after surgery so that you can breathe on your own again sooner. It does this by binding to rocuronium bromide or vecuronium bromide in your body. It can be used in adults when rocuronium bromide or vecuronium bromide is used, and in children and adolescents (between 2 and 17 years) when rocuronium bromide is used for moderate muscle relaxation.
You should not be given Sugammadex Normon
If you are allergic to sugammadex or any of the other ingredients of this medicine (listed in section 6).
Tell your anesthesiologist if this applies to you.
Warnings and precautions
Talk to your anesthesiologist before you start using Sugammadex Normon
Children and adolescents
This medicine is not recommended for children under 2 years of age.
Other medicines and Sugammadex Normon
Tell your anesthesiologist if you are taking, have recently taken, or might take any other medicines.
Sugammadex Normon may affect other medicines or be affected by them.
Some medicines reduce the effect of Sugammadex Normon
It is especially important that you tell your anesthesiologist if you have recently taken:
Sugammadex Normon may affect hormonal contraceptives
Sugammadex may make hormonal contraceptives such as the "Pill", vaginal ring, implants, or an Intrauterine Hormonal Device (IUD-h) less effective because it reduces the amount of progestogen that reaches you. The amount of progestogen lost due to the use of Sugammadex Normon is approximately the same as when you miss a birth control pill.
Effects on blood tests
In general, Sugammadex Normon does not affect laboratory tests. However, it may affect the results of a blood test when progesterone levels are measured. Talk to your doctor if your progesterone levels need to be analyzed on the same day that you receive Sugammadex Normon.
Pregnancy and breastfeeding
Tell your anesthesiologist if you are pregnant or think you may be pregnant or if you are breastfeeding.
Sugammadex Normon may still be given to you, but this needs to be discussed beforehand.
It is not known whether sugammadex passes into breast milk. Your anesthesiologist will help you decide whether to stop breastfeeding or avoid treatment with sugammadex, considering the benefit of breastfeeding to the baby and the benefit of Sugammadex Normon to the mother.
Driving and using machines
Sugammadex Normon has no known influence on the ability to drive and use machines.
Sugammadex Normon contains sodium
This medicine contains up to 9.3 mg of sodium (a major component of cooking/table salt) per ml. This is equivalent to 0.5% of the maximum recommended daily intake of sodium for an adult.
Sugammadex Normon will be administered to you by your anesthesiologist or under their supervision.
Dose
Your anesthesiologist will calculate the dose of Sugammadex Normon that you need based on:
The usual dose is 2-4 mg per kg of body weight. A dose of 16 mg/kg may be used in adults if urgent recovery from muscle relaxation is needed.
The dose of Sugammadex Normon for children is 2.4 mg/kg (children and adolescents between 2 and 17 years).
How Sugammadex Normon is administered
Sugammadex Normon will be administered to you by your anesthesiologist. It is injected once into a vein.
If you are given more Sugammadex Normon than recommended
Since your anesthesiologist will be carefully monitoring the situation, it is unlikely that you will be given too much Sugammadex Normon. But even if this happens, it is unlikely to cause any problems.
If you have any further questions on the use of this medicine, ask your anesthesiologist or another doctor.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If these side effects occur while you are under anesthesia, your anesthesiologist will detect and treat them.
Common (may affect up to 1 in 10 people)
Uncommon (may affect up to 1 in 100 people)
Frequency not known
Reporting of side effects
If you experience any side effects, talk to your anesthesiologist or another doctor, even if they are not listed in this leaflet. You can also report side effects directly through the Spanish Medicines and Healthcare Products Agency (AEMPS) website: www.notificaRAM.es
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.
Storage will be the responsibility of healthcare professionals.
Do not use this medicine after the expiry date which is stated on the label and carton after "EXP". The expiry date is the last day of the month stated.
Store below 30°C. Do not freeze. Keep the vial in the outer packaging to protect it from light.
After opening and dilution, store at 2-8°C and use within 24 hours.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Composition of Sugammadex Normon
Appearance and pack size
Sugammadex Normon is a clear, colorless to slightly yellow-brown solution for injection. It comes in two different pack sizes, 10 vials of 2 ml or 10 vials of 5 ml of solution for injection.
Not all pack sizes may be marketed.
Marketing authorization holder and manufacturer
LABORATORIOS NORMON, S.A.
Ronda de Valdecarrizo, 6
28760 Tres Cantos
Madrid (SPAIN)
Date of last revision of this leaflet:December 2022
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Healthcare Products (AEMPS) (http://www.aemps.gob.es/)
This information is intended only for healthcare professionals:
For detailed information, consult the Summary of Product Characteristics or the Package Leaflet of Sugammadex Normon 100 mg/ml solution for injection EFG.
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