Cisatracurium
Cisatracurium Accordpharma contains the active substance cisatracurium, in the form of cisatracurium besylate, which belongs to a group of medicines called muscle relaxants.
Cisatracurium Accordpharma is used:
To obtain additional information about the use of the medicine, consult a doctor.
Do not use Cisatracurium Accordpharma if any of the above situations apply to the patient.
In case of doubts, consult a doctor, nurse, or pharmacist before starting to use Cisatracurium Accordpharma.
Before starting to take Cisatracurium Accordpharma, discuss it with a doctor, nurse, or pharmacist:
In case of doubts whether any of the above situations apply to the patient, consult a doctor, nurse, or pharmacist before starting to use Cisatracurium Accordpharma.
Tell the doctor about all medicines the patient is currently taking or has recently taken, as well as any medicines the patient plans to take.
Particularly, inform the doctor about the use of the following medicines:
The harmful effect of cisatracurium on the breastfed child cannot be excluded, however, it is not expected to have an effect if breastfeeding is resumed after the effect of the medicine has ceased. Cisatracurium is rapidly eliminated from the body. The woman should not breastfeed for 3 hours after the administration of the medicine has ended.
In case the patient is in the hospital for only one day, the doctor will inform the patient when they can leave the hospital or drive a car. Driving a car too soon after surgery may be dangerous.
The patient will never take this medicine by themselves. The medicine will always be administered to the patient by a qualified person.
Cisatracurium Accordpharma can be administered as:
The method of administration and dose of Cisatracurium Accordpharma will be decided by the doctor, based on:
This medicine should not be used in children under 1 month of age.
Cisatracurium Accordpharma will always be administered under close supervision. However, if the patient thinks they may have received too much medicine, they should immediately inform their doctor or nurse.
In case of any further doubts about the use of this medicine, consult a doctor.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If any side effects are observed, the doctor, nurse, or pharmacist should be informed immediately. This also applies to side effects not listed in this leaflet.
If an allergic reaction occurs, the doctor or nurse should be informed immediately.
Symptoms of an allergic reaction may include:
The doctor, nurse, or pharmacist should be informed if the patient notices any of the following side effects:
If any side effects occur, including those not listed in the leaflet, the doctor or pharmacist should be informed. Side effects can be reported directly to the Department of Pharmacovigilance of the 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
Reporting side effects can help gather more information on the safety of the medicine.
Side effects can also be reported to the marketing authorization holder.
Store the medicine out of sight and reach of children.
Do not use this medicine after the expiry date stated on the carton and on the vial after: EXP.
The expiry date refers to the last day of the month.
Store in a refrigerator (2°C - 8°C). Do not freeze.
Store in the original packaging to protect from light.
The diluted solution should be stored at 2°C - 8°C and used within 24 hours. After 24 hours, any unused solution should be discarded.
Medicines should not be disposed of via wastewater or household waste. Ask a pharmacist how to dispose of medicines no longer required. This will help protect the environment.
1 mL of solution for injection/infusion contains 2 mg of cisatracurium, in the form of 2.68 mg of cisatracurium besylate.
One 2.5 mL vial of solution for injection/infusion contains 5 mg of cisatracurium, in the form of 6.7 mg of cisatracurium besylate.
One 5 mL vial of solution for injection/infusion contains 10 mg of cisatracurium, in the form of 13.4 mg of cisatracurium besylate.
One 10 mL vial of solution for injection/infusion contains 20 mg of cisatracurium, in the form of 26.8 mg of cisatracurium besylate.
The other ingredients are: benzenesulfonic acid, solution, and water for injections.
Cisatracurium Accordpharma, 2 mg/mL, is a solution for injection/infusion, colorless to pale yellow or greenish-yellow, practically free from visible particles, with a pH of 3.0-5.0.
Not all pack sizes may be marketed.
Accord Healthcare Polska Sp. z o.o.
ul. Taśmowa 7
02-677 Warsaw
Tel: +48 22 577 28 00
Ronda de Los Olivares, parcela 11
Pol. Ind. Los Olivares,
23009 Jaén, Spain
Member State | Authorization Name |
Austria | Cisatracurium Accordpharma 2 mg/mL solution for injection/infusion |
Belgium | Cisatracurium Accordpharma 2 mg/mL oplossing voor injectie / infusie, solution injectable/pour perfusion, Injektions-/Infusionslösung |
Croatia | Cisatracurium 2mg/mL otopina za injekciju/infuziju |
Cyprus | Cisatracurium Accordpharma 2 mg/mL solution for injection/infusion |
Denmark | Cisatracurium Accordpharma |
Finland | Cisatracurium Accordpharma 2 mg/mL injektio/infuusioneste, liuos |
France | Cisatracurium Accordpharma 2 mg/mL solution injectable/pour perfusion |
Netherlands | Cisatracurium Accordpharma 2 mg/mL oplossing voor injectie of infusie |
Germany | Cisatracurium Accordpharma 2 mg/mL Injektions-/Infusionslösung |
Norway | Cisatracurium Accordpharma |
Poland | Cisatracurium Accordpharma |
Portugal | Cisatracúrio Accordpharma |
Hungary | Cisatracurium Accordpharma 2 mg/mL solution for injection/infusion |
Italy | Cisatracurio Accordpharma |
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