Cisatracurium
For the rest of this leaflet, Cisatracurium Noridem will be called Cisatracurium.
The active substance is Cisatracurium besylate, which belongs to a group of medicines called muscle relaxants.
Cisatracurium is used:
Consult a doctor, nurse, or pharmacist:
If in doubt whether any of the above applies to the patient, consult a doctor or nurse before using Cisatracurium.
Tell your doctor about all medicines the patient is taking or has recently taken, including herbal products and those bought without a prescription.
In particular, tell your doctor if the patient is taking any of the following medicines:
If the patient is pregnant or breastfeeding, thinks she may be pregnant, or plans to have a baby, she should consult a doctor before using this medicine.
The risk of Cisatracurium to the breastfed child cannot be excluded, however, it is not expected to affect the child if breastfeeding is resumed after the effects of Cisatracurium have worn off.
Cisatracurium is rapidly eliminated from the body. The woman should not breastfeed for 3 hours after the end of the administration of Cisatracurium.
If the patient is in the hospital for only one day, the doctor will decide how long to wait before leaving the hospital or driving a vehicle. Driving too soon after surgery can be dangerous.
The patient will never use this medicine by themselves. Cisatracurium will always be given to the patient by a qualified person.
Cisatracurium can be given:
Cisatracurium should not be used in children under 1 month old.
Cisatracurium will always be given under medical supervision. However, if the patient thinks they have been given too much medicine, they should tell their doctor or nurse immediately.
If the patient has any further questions about the use of this medicine, they should ask their doctor.
Like all medicines, Cisatracurium can cause side effects, although not everybody gets them.
If any of the side effects get serious, or if the patient notices any side effects not listed in this leaflet, they should tell their doctor.
If an allergic reaction occurs, the patient should tell their doctor or nurse immediately.
Possible symptoms:
If the patient experiences any of the following symptoms, they should tell their doctor or nurse:
If the patient experiences any side effects, including those not listed in this leaflet, they should tell their doctor, pharmacist, or nurse. Side effects can be reported directly to the
Department of Post-Marketing Surveillance of Adverse Reactions to Medicinal Products, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products,
Jerozolimskie Avenue 181C,
02-222 Warsaw,
Phone: +48 22 49 21 301,
Fax: +48 22 49 21 309,
Website: https://smz.ezdrowie.gov.pl.
Reporting side effects will help to gather more information on the safety of this medicine.
Cisatracurium is packaged in transparent glass ampoules, in boxes of 5 and 1 piece each.
Each 10 ml ampoule contains 20 mg of cisatracurium.
Each 5 ml ampoule contains 10 mg of cisatracurium.
Each 2.5 ml ampoule contains 5 mg of cisatracurium.
Not all pack sizes may be marketed.
Marketing Authorization Holder:Noridem Enterprises Limited, Evagorou & Makariou, Mitsi Building 3,
Office 115, 1065 Nicosia, Cyprus.
Manufacturer:DEMO S.A., PHARMACEUTICAL INDUSTRY 21 km National Road Athens-Lamia,
14568 Krioneri, Attica, Greece, T:+30 210 8161802, F:+30 2108161587.
IE: Cisatracurium 2 mg/ml Solution for injection/infusion
EL: CISATRAL 2 mg/ml Διάλυμα για ένεση/έγχυση
DE: Cisatracurium Noridem 2 mg/ml Injektions-/Infusionslösung
AT: Cisatracurium Noridem 2 mg/ml Injektions-/Infusionslösung
PL: Cisatracurium Noridem
Date of last revision of the leaflet:10/2024
The product is for single use only. Only clear and almost colorless yellow or greenish-yellow solutions should be used. Before administration, the appearance of the solution should be checked. If the appearance of the solution is changed or the container is damaged, the product should be discarded.
The diluted Cisatracurium Noridem product is physically and chemically stable for at least 24 hours at 5°C and 25°C at concentrations of 0.1 – 1 mg/ml in the following infusion solutions, in polypropylene containers:
sodium chloride 0.9% w/v solution for infusion
glucose 5% w/v solution for infusion
sodium chloride 0.18% w/v and glucose 4% w/v solution for infusion
sodium chloride 0.45% w/v and glucose 2.5% w/v solution for infusion
However, since the product does not contain antimicrobial preservatives, it should be diluted immediately before use. Otherwise, it should be stored in accordance with the recommendations given in section 6.3.
Under simulated Y-site infusion conditions, Cisatracurium Noridem has been shown to be compatible with the following commonly used perioperative medicines: fentanyl citrate and midazolam hydrochloride.
If other medicines are administered through the same intravenous line or cannula as Cisatracurium Noridem, it is recommended that the line or cannula be flushed with a suitable infusion solution, such as sodium chloride 0.9% w/v solution for infusion, between each medicine administration.
As with other intravenous medicines, if a small vein is chosen for injection, the vein should be flushed with a suitable infusion solution, such as sodium chloride 0.9% w/v solution for infusion, after administration of Cisatracurium Noridem.
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