PATIENT INFORMATION LEAFLET
Sodium Iodide (131I) Curium Pharma Spain 37-7400 MBq hard capsule
Sodium Iodide (131I)
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack:
Sodium Iodide (131I) is a medicine used in adults, children, and adolescents to treat:
This medicine contains Sodium Iodide (131I), a radioactive element that accumulates in certain organs such as the thyroid gland.
This medicine is radioactive, but your doctor and nuclear medicine doctor have considered that the beneficial effect of this medicine on your health outweighs the risk due to radiation.
Do not use Sodium Iodide (131I) if
If any of these cases apply to you, tell your nuclear medicine doctor.
Warnings and precautions
Tell your nuclear medicine doctor in the following cases:
Consult your nuclear medicine doctor if you are in any of the above situations. It is possible that Sodium Iodide (131I) may not be suitable for you. Your doctor will inform you if you need to take special precautions after using this medicine. Talk to your nuclear medicine doctor if you have any questions.
In elderly patients who have had their thyroid removed, low sodium levels in the blood have been observed. This phenomenon is more likely to occur in women and patients taking medications that increase the amount of water and sodium excreted in the urine (diuretics, such as hydrochlorothiazide). If you are in one of these groups, your doctor may perform periodic blood tests to check the amount of electrolytes (such as sodium) in your blood.
Before administration of Sodium Iodide (131I)you should:
Children and adolescents
Tell your nuclear medicine doctor if your child is under 18 years old or cannot swallow a capsule.
Other medicines and Sodium Iodide (131I)
Tell your nuclear medicine doctor if you are taking, have recently taken, or may need to take any other medicine, including those bought without a prescription.
Tell your nuclear medicine doctor if you are taking or have recently taken any of the following medicines or products, as they may affect the effectiveness of this treatment.
It is possible that your doctor may recommend stopping the use of the following medicines before treatment:
Using Sodium Iodide (131I) with food
Your doctor may recommend that you follow a low-iodine diet before treatment and avoid certain foods such as seafood and shellfish.
Pregnancy and breast-feeding
This medicine must not be used during pregnancy. Therefore, tell your nuclear medicine doctor before taking Sodium Iodide (131I)if you might be pregnant, if you have a delayed menstrual period, think you might be pregnant, or plan to become pregnant.
If you are pregnant
Do not takeSodium Iodide (131I). Any possibility of pregnancy must be ruled out before using this medicine.
Contraception in men and women
Women should avoid becoming pregnant for at least 6 months after administration of Sodium Iodide (131I). Women are advised to use contraceptive methods for a period of 6 months after treatment.
As a precaution, men should avoid fathering a child for a period of 6 months after treatment with Sodium Iodide (131I) to allow for the replacement of irradiated sperm with non-irradiated sperm.
Fertility
Treatment with Sodium Iodide (131I) may temporarily reduce fertility in men and women.
In men, high doses of Sodium Iodide (131I) may temporarily affect sperm production. If you ever wish to have a child, talk to your doctor about how to conserve your semen in a sperm bank.
If you are breast-feeding:
Tell your doctor if you are breast-feeding, as you should stop breast-feeding 8 weeks before treatment. Breast-feeding should not be resumed after treatment with Sodium Iodide (131I).
Driving and using machines
It is unlikely that Sodium Iodide (131I) will affect your ability to drive or use machines.
Sodium Iodide (131I) contains sodium and sugar
This medicine contains 63.5 mg of sodium (the main component of table/cooking salt) per capsule. This is equivalent to 3% of the maximum recommended daily intake of sodium for an adult. This should be taken into account if you are on a low-sodium diet.
This medicine contains sucrose, a type of sugar. If your doctor has told you that you have an intolerance to certain sugars, consult them before taking this medicine.
There are strict rules on the use, handling, and disposal of radiopharmaceuticals. Sodium Iodide (131I) will only be used in controlled areas. This medicine will only be handled and administered by properly trained and qualified personnel to use it safely. These personnel will take special safety measures for the safe use of this medicine and will inform you accordingly.
The nuclear medicine doctor supervising the procedure will decide the amount of Sodium Iodide (131I) you should take. It will be the minimum amount necessary to achieve the desired effect.
Sodium Iodide (131I) is administered in a single capsule by specialists who will take the necessary precautions.
The recommended doses for an adult are:
MBq (megabecquerel) is the unit used to measure the amount of radioactivity of the medicine.
Use in children and adolescents under 18 years
Lower doses are used for children and adolescents.
How Sodium Iodide (131I) is administered and what the procedure is
You will be given a single capsule of Sodium Iodide (131I).
Your stomach should be empty when you take the capsule.
Take the capsule with plenty of water so that it reaches your stomach as quickly as possible.
Young children should take the capsule with pureed food.
Drink as much water as possible after taking the capsule and on the day after treatment. This will eliminate the active ingredient from your bladder.
Duration of the procedure
Your nuclear medicine doctor will tell you the duration of the procedure.
After administration of Sodium Iodide (131I)
Your nuclear medicine doctor will inform you if you need to take any special precautions after receiving this medicine. In particular, you should:
Your blood, feces, urine, or possible vomit may be radioactive for a few days, and you should not be in contact with other people.
Consult your nuclear medicine doctor if you have any questions.
If you receive more Sodium Iodide (131I) than you should
It is very unlikely that an overdose will occur, as you will receive only a single dose of Sodium Iodide (131I) under the strict control of the nuclear medicine doctor supervising the procedure.
However, if this happens, your doctor will administer the appropriate treatment.
If you have any further questions on the use of Sodium Iodide (131I), ask your nuclear medicine doctor supervising the procedure.
Like other medications, this medication may produce adverse effects, although not all people suffer from them.
Frequent adverse reactions are: hypothyroidism (underactive thyroid gland), temporary hyperthyroidism (overactive thyroid gland), disorders of the salivary and lacrimal glands, and local radiation effects. In cancer treatment, frequent adverse effects on the stomach and intestines and a reduction in blood cell production in the bone marrow may also occur.
If you have a severe allergic reaction that causes difficulty breathing or dizziness, or if you have a severe hyperthyroid crisis, contact your doctor immediately.
Below, all the adverse effects of Sodium Iodide (131I) are listed, grouped according to the indication for which it is used, as they depend on the doses used for the different treatments.
Treatment of Hyperactive Thyroid Gland
Very Common(may affect more than 1 in 10 people):
Common(may affect up to 1 in 10 people):
Very Rare(may affect up to 1 in 10,000 people):
Frequency Not Known(frequency cannot be estimated from available data):
Cancer Treatment
Very Common(may affect more than 1 in 10 people):
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(frequency cannot be estimated from available data):
Reporting of Adverse Effects:
If you experience any type of adverse effect, consult your nuclear medicine doctor, even if it is a possible adverse effect that does not appear in this prospectus. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
You will not have to store this medication. This medication is stored under the responsibility of the specialist in suitable facilities. The storage of radiopharmaceuticals must comply with national regulations for radioactive materials.
The following information is intended only for specialists.
Sodium Iodide (131I) should not be used after the expiration date shown on the label after "EXP".
Do not store above 25°C.
Composition of Sodium Iodide (131I)
Gelatin (in the capsule shell), disodium phosphate dihydrate, sodium thiosulfate, sodium hydrogencarbonate, sodium hydroxide, sucrose, sodium chloride, and water for injectable preparations.
Appearance of the Product and Package Contents
Sodium Iodide (131I) is a transparent capsule with a white to slightly brown powder, presented in packages containing one capsule.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder:
Curium Pharma Spain S.A.
Avenida Doctor Severo Ochoa Nº 29
28100, Alcobendas, Madrid
Manufacturer:
Curium Netherlands B.V.
Westerduinweg 3
1755 LE Petten
Netherlands
This prospectus was approved in November 2021.
Detailed information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/).
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This information is intended only for doctors or healthcare professionals:
The complete technical sheet of Sodium Iodide (131I) Curium Pharma Spain 37-7400 MBq hard capsule is included at the end of this prospectus, in order to provide doctors or healthcare professionals with scientific information and practical information on the administration and use of this radiopharmaceutical.
Please consult the technical sheet of Sodium Iodide (131I).