Package Leaflet: Information for the User
VISIPAQUE 270 mg/ml, Solution for Injection
VISIPAQUE 320 mg/ml, Solution for Injection
Iodixanol
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
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Contents of the Package Leaflet:
This medicine is for diagnostic use only.
It is used to help identify a disease.
VISIPAQUE is a "contrast medium". It is given before an X-ray examination to make the image taken by your doctor clearer.
It can also be used to examine the esophagus, stomach, and intestine, or to visualize body cavities, such as joints, uterus, and fallopian tubes. Your doctor will explain which part of your body will be examined.
Do not use VISIPAQUE:
Warnings and precautions
Talk to your doctor before you are given Visipaque:
During or shortly after the diagnostic imaging procedure, you may experience a short-term brain disorder called encephalopathy. Tell your doctor immediately if you notice any of the symptoms related to this condition described in Section 4.
Thyroid disorders may be observed after Visipaque administration in both children and adults. Babies may also be exposed through the mother during pregnancy. Your doctor may need to perform thyroid function tests before and/or after Visipaque administration.
If you are not sure if any of the above applies to you, talk to your doctor before using VISIPAQUE.
Tell your doctor if you are taking, have recently taken, or might take any other medicines.
In diabetic patients who are taking a medicine that contains metformin.
In patients who are taking medicines that suppress the immune system, such as transplant medicines (interleukin-2).
In patients who are taking medicines to lower blood pressure (beta-blockers)
If you are pregnant or breastfeeding, or think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine.
The product should not be used during pregnancy unless the benefit outweighs the risk and is considered essential by the doctor.
If Visipaque was administered to the mother during pregnancy, it is recommended to monitor the thyroid function of the babies.
Driving and using machines:
Do not drive or use tools or machines after VISIPAQUE administration for:
The reason is that you may feel dizzy or have other symptoms of a late reaction.
VISIPAQUE contains sodium chloride and calcium and sodium edetate.
VISIPAQUE 270 mg/ml: patients on low-sodium diets should be aware that this medicine contains 0.76 mg (0.03 mmol) of sodium per ml.
VISIPAQUE 320 mg/ml: patients on low-sodium diets should be aware that this medicine contains 0.45 mg (0.02 mmol) of sodium per ml.
VISIPAQUE will always be administered by qualified and trained personnel.
Follow your doctor's instructions for administering this medicine exactly. If you are unsure, ask your doctor again.
Your doctor will decide the dose that is best for you. The recommended dose is:
After VISIPAQUE administration, you will be asked
If you experience any side effects during this time, tell your doctor immediately (see section 4 "Possible side effects").
The above recommendation applies to all patientswho have received VISIPAQUE. If you have not understood something from the above, ask your doctor.
VISIPAQUE can be administered in many different ways, a description of the ways it is usually administered can be found below:
Injection into an artery or vein
VISIPAQUE is injected into a vein in the arm or leg or administered through a thin plastic tube (catheter), usually in an artery in the arm or groin.
Injection into the spine
VISIPAQUE is injected into the space surrounding the spinal cord to visualize the spinal canal. If you have been administered VISIPAQUE in the spine, you will be asked to follow the recommendations indicated below:
The above recommendation only applies if you have been injected with VISIPAQUE in the spine. If you have not understood something from the above, ask your doctor.
Use in body cavities or jointsBody cavities such as joints, uterus, and fallopian tubes. How and where VISIPAQUE will be administered will vary from one to another.
Oral useFor the examination of the esophagus, stomach, or small intestine, VISIPAQUE is usually administered orally. In children, it is also administered rectally.
Like all medicines, VISIPAQUE can cause side effects, although not everybody gets them.
Allergic reactionsIf you experience an allergic reaction when VISIPAQUE is being administered to you in a hospital or clinic, tell the doctor immediately. The symptoms can be:
The side effects described above can occur several hours or days after VISIPAQUE administration. If any of these side effects occur after you leave the hospital or clinic, go directly to the emergency department of your nearest hospital.
Other side effects you may experience are the following, which will depend on how or why VISIPAQUE was administered to you. Ask your doctor if you are not sure how VISIPAQUE was administered to you.
After injection into an artery or veinUncommon(affects less than 1 in 100 people)
Rare(affects less than 1 in 1,000 people)
Very rare(affects less than 1 in 10,000 people)
Frequency not known
After injection into the spine (intrathecal)Uncommon(affects less than 1 in 100 people)
Frequency not known(cannot be estimated from the available data)
After administration into body cavities(such as uterus and fallopian tubes)Very common(affects more than 1 in 10 people)
Common(affects less than 1 in 10 people)
Uncommon(affects less than 1 in 100 people)
Frequency not known(cannot be estimated from the available data)
After injection into the jointsCommon(affects less than 1 in 10 people)
Frequency not known(cannot be estimated from the available data)
After oral administrationCommon(affects less than 1 in 10 people)
Uncommon(affects less than 1 in 100 people)
Frequency not known(cannot be estimated from the available data)
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Spanish Pharmacovigilance System for Human Use Medicines: https://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.
Store below 30°C. Store in the outer packaging to protect from light.
Do not use this medicine after the expiry date stated on the packaging after EXP.
The expiry date is the last day of the month indicated.
Composition of VISIPAQUE
The active substance is Iodixanol:
One ml of solution contains 550 mg of Iodixanol (equivalent to 270 mg of iodine)
One ml of solution contains 652 mg of Iodixanol (equivalent to 320 mg of iodine)
The other ingredients are:
trometamol, sodium chloride, calcium chloride, calcium and sodium edetate, hydrochloric acid (pH adjustment), and water for injections. (See section 2 VISIPAQUE contains sodium chloride and calcium and sodium edetate).
Appearance and packaging
VISIPAQUE is presented ready for use as a clear, colorless or slightly yellowish aqueous solution.
It is available in two concentrations:
Presentation:
VISIPAQUE 270 mg/ml – 1 and 10 vials of 50, 75, 100, 200, and 1 and 6 vials of 500 ml.
VISIPAQUE 320 mg/ml – 1 and 10 vials of 50, 100, 200, and 1 and 6 vials of 500 ml.
The 50 ml, 75 ml, 100 ml, and 200 ml vials are single-dose.
The 500 ml vials are multi-dose.
Not all pack sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder:
GE Healthcare Bio-Sciences, S.A.U.
Calle Gobelas, 35-37, La Florida
28023, Madrid
Manufacturer:
GE Healthcare Ireland Limited
IDABusinessPark
Carrigtohill
Co. Cork, Ireland
or
GE Healthcare AS.
Nycoveien, 1
NO-0485 Oslo
Norway
Date of last revision of thisleaflet: April 2022
Detailed and up-to-date information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.es