Sugammadex
Sugammadex Orion contains the active substance sugammadex. Sugammadex Orion is considered a selective relaxant binding agentbecause it only works with certain muscle relaxants - rocuronium bromide or vecuronium bromide.
In some types of surgery, the patient's muscles must be completely relaxed. This allows the surgeon to perform the operation more easily. To achieve this, muscle relaxants are given during general anaesthesia. These are called muscle relaxantsand include rocuronium bromide and vecuronium bromide. Because these medicines also cause relaxation of the respiratory muscles, assisted breathing (artificial ventilation) is necessary during and after surgery until the patient's own breathing returns. Sugammadex Orion is used to speed up the recovery of the muscles after surgery, so that the patient can breathe on their own again sooner. Its action involves binding to rocuronium bromide or vecuronium bromide in the body. The medicine can be used in adults when rocuronium bromide or vecuronium bromide has been given. It can be used in newborns, infants, small children, children, and adolescents (from birth to 17 years) when rocuronium bromide has been given.
Before Sugammadex Orion is given, discuss this with your anaesthesiologist
Tell your anaesthesiologist about all medicines you are taking or have recently taken, as well as any medicines you plan to take. Sugammadex Orion may affect the action of other medicines, or other medicines may affect the action of Sugammadex Orion. Some medicines reduce the effectiveness of Sugammadex Orion. It is especially important to inform your anaesthesiologist if you have taken the following medicines recently:
Sugammadex Orion may affect the effectiveness of hormonal contraceptives
Sugammadex Orion usually does not affect laboratory test results. However, it may affect the results of blood tests for a hormone called progesterone. If your progesterone level is to be tested on the same day that Sugammadex Orion is given, inform your doctor.
Inform your anaesthesiologist if you are pregnant or think you may be pregnant, or if you are breastfeeding. Sugammadex Orion can still be used in pregnant women, but this should be discussed with your doctor first. It is not known whether sugammadex passes into breast milk. Your anaesthesiologist will help you decide whether to stop breastfeeding or avoid treatment with Sugammadex Orion, considering the benefits of breastfeeding for your baby and the benefits of treatment with Sugammadex Orion for you.
The effect of Sugammadex Orion on the ability to drive and use machines is not known.
The medicine contains up to 9.5 mg of sodium (the main component of common salt) per ml of solution for injection. This is equivalent to 0.5% of the maximum recommended daily intake of sodium in the diet for adults.
Sugammadex Orion will be given to you by your anaesthesiologist or under the supervision of your anaesthesiologist.
Your anaesthesiologist will adjust the dose of Sugammadex Orion based on:
The usual dose is from 2 mg/kg body weight to 4 mg/kg body weight in patients of all ages. If rapid recovery of muscle function is needed, a dose of 16 mg/kg body weight can be given to adults.
Sugammadex Orion is given by your anaesthesiologist. It is given as a single injection through a vein.
Because your anaesthesiologist closely monitors your condition, it is unlikely that you will be given too much Sugammadex Orion. However, if this happens, no problems should occur. If you have any further questions about the use of this medicine, ask your anaesthesiologist or another doctor.
Like all medicines, Sugammadex Orion can cause side effects, although not everybody gets them. If these side effects occur during anaesthesia, they will be noticed and treated by your anaesthesiologist. Common (may affect up to 1 in 10 people)
Uncommon (may affect up to 1 in 100 people)
Rare (may affect up to 1 in 1,000 people)
Frequency not known (cannot be estimated from the available data)
If you experience any side effects, including any not listed in this package leaflet, tell your anaesthesiologist or another doctor. Side effects can be reported directly to the Department of Drug Safety, Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, Tel.: +48 22 49 21 301, Fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl. Side effects can also be reported to the marketing authorisation holder. By reporting side effects, you can help provide more information on the safety of this medicine.
The medicine will be stored by healthcare professionals. Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date which is stated on the carton and label after "EXP". The expiry date refers to the last day of that month. Do not freeze. Store the vials in the outer carton to protect from light. After first opening and dilution, store in a refrigerator (2°C - 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.
Sugammadex Orion is a clear solution for injection, colourless to slightly yellow, practically free from particles. Pack sizes: 10 vials of 2 ml.
Orion Corporation, Orionintie 1, FI-02200 Espoo, Finland
Orion Corporation, Orion Pharma, Orionintie 1, FI-02200 Espoo, Finland, Orion Corporation, Orion Pharma, Joensuunkatu 7, FI-24100 Salo, Finland. For further information about this medicine, contact the local representative of the marketing authorisation holder: Orion Pharma Poland Sp. z o.o., kontakt@orionpharma.info.pl, Date of last revision of the package leaflet:05/2025
For detailed information, refer to the Summary of Product Characteristics for Sugammadex Orion.
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