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SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION

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About the medicine

How to use SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION

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This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.

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Introduction

PACKAGE LEAFLET: INFORMATION FOR THE USER

Sodium Iodide (123I) Curium Pharma Spain 37 MBq/ml injectable solution

Sodium Iodide (123I)

Read all of this leaflet carefully before you start using this medicine.

  • Keep this leaflet, you may need to read it again.
  • If you have any further questions, ask your doctor or pharmacist.
  • This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.
  • If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet.

Contents of the package leaflet:

  1. What Sodium Iodide (123I) Curium Pharma Spain 37 MBq/ml injectable solution is and what it is used for.
  2. Before you use Sodium Iodide (123I) Curium Pharma Spain 37 MBq/ml injectable solution
  3. How to use Sodium Iodide (123I) Curium Pharma Spain 37 MBq/ml injectable solution
  4. Possible side effects
  5. Storage of Sodium Iodide (123I) Curium Pharma Spain 37 MBq/ml injectable solution
  6. Package contents and further information

1. What Sodium Iodide (123I) Curium Pharma Spain 37 MBq/ml injectable solution is and what it is used for

This medicinal product is for diagnostic use only.

It belongs to a group of medicinal products called other radiopharmaceuticals for cardiovascular system diagnosis. When injected, it temporarily accumulates in the thyroid gland. Because the radiopharmaceutical contains a small amount of radioactivity, it can be detected from outside the body using a special medical device called a gamma camera, and an image known as a scintigram can be obtained. This scintigram will show the exact location and distribution of the radiopharmaceutical in the organs and tumors where it accumulates, providing the doctor with valuable information about the shape and function of the thyroid glands.

Doctor consultation

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2. Before you use Sodium Iodide (123I) Curium Pharma Spain 37 MBq/ml injectable solution

Before administering this medicine, you must ensure that you are well hydrated.

Do not use Sodium Iodide (123I) Curium Pharma Spain:

  • If you are breastfeeding.
  • If you are allergic (hypersensitive) to the active substance or any of the other components of Sodium Iodide (123I) Curium Pharma Spain.

Be cautious with Sodium Iodide (123I) Curium Pharma Spain:

Sodium Iodide (123I) Curium Pharma Spain is a radiopharmaceutical and, therefore, its administration involves the administration of relatively high doses of radiation (radioactivity) in most patients (see "POSSIBLE SIDE EFFECTS").

If you have kidney problems, the activity you receive should be adjusted.

If you are under 18 years old because exposure to radiation is proportionally greater than in adults.

Use of other medicines:

Tell your doctor or pharmacist if you are using or have recently used any other medicines, including those obtained without a prescription.

Some medicines may cause Sodium Iodide (123I) Curium Pharma Spain to not work properly:

  • Thyroid inhibitors, carbimazole (or other imidazole derivatives such as propylthiouracil), salicylates, steroids, sodium nitroprusside, sodium sulfobromophthalein, perchlorate, and various agents (anticoagulants, antihistamines, antiparasitics, penicillins, sulfonamides, tolbutamide, thiopentone) are usually suspended 1 week before administration of Sodium Iodide (123I) Curium Pharma Spain.
  • Phenylbutazone is usually suspended 1-2 weeks before.
  • Expectorants and vitamins, 2 weeks before.
  • Natural or synthetic thyroid preparations (sodium thyroxine, sodium liotironine, thyroid extract), 2-6 weeks before.
  • Amiodarone, benzodiazepines, lithium, 4 weeks before.
  • Skin disinfectants containing iodine, 1-9 months before.
  • Intravenous contrast agents, oral cholecystographic agents, and contrast media containing iodine, for periods of up to 1 year before treatment.

Pregnancy and breastfeeding

Consult your doctor or pharmacist before using any medicine.

If you are a woman of childbearing age (age at which you can become pregnant)you should always rule out pregnancy. If you experience a delay in your menstrual period, you should consider the possibility that you are pregnant until proven otherwise. In case of doubt, it is essential that radiation exposure is minimal and necessary to obtain the desired clinical information. The possibility of using alternative techniques that do not involve ionizing radiation should be considered.

If you are pregnantyou should not receive this medicine unless it is strictly necessary because the fetus will receive a small amount of radiation, or when the benefit to you outweighs the risk to the fetus.

If you are breastfeeding your child:Before administering Sodium Iodide (123I) Curium Pharma Spain to a breastfeeding mother, the possibility of delaying the examination until the mother has stopped breastfeeding should be considered, and it should be determined whether the most suitable radiopharmaceutical has been selected, taking into account the secretion of activity in breast milk. If administration during breastfeeding is unavoidable, breastfeeding should be suspended for 1.5-3 days after administration of this medicine, as it contains iodine-123 and iodine-124 and iodine-125 as contaminants, and the expressed milk should be discarded during this period. The possibility of expressing milk before administration of this product and storing it for later use should be considered. Breastfeeding can be resumed when the level of radioactivity in breast milk does not pose a radiation dose to the child greater than 1 mSv.

Driving and using machines

No effects on the ability to drive or use machines are expected after using this medicine.

Important information about some of the components of Sodium Iodide (123I) Curium Pharma Spain

This medicine contains less than 23 mg (1 mmol) of sodium per dose, so it is considered essentially "sodium-free".

3. How to use Sodium Iodide (123I) Curium Pharma Spain 37 MBq/ml injectable solution

This medicine should be administered exclusively by authorized personnel who will indicate the instructions to follow at all times.

Your doctor will decide the amount of this medicine that will be administered to you. This will be the minimum amount necessary to obtain a scintigram with the necessary quality to provide the required information.

For detailed instructions on the correct administration/use of Sodium Iodide (123I) Curium Pharma Spain, see section 6.

If you think the action of Sodium Iodide (123I) Curium Pharma Spain is too strong or too weak, tell your doctor or pharmacist.

If you are given more Sodium Iodide (123I) Curium Pharma Spain than you should be

Since this product is administered by a doctor under strict control conditions, any overdose is very unlikely.

However, in the event that you are administered an excessive dose of this medicine, the absorbed radiation dose should be reduced by increasing the elimination of the radiopharmaceutical from the body, for which you will be recommended to frequently empty your bladder and stimulate gastrointestinal transit.

In case of overdose or accidental ingestion, consult the Toxicology Information Service. Telephone 91 5620420.

If you have any further questions about the use of this product, ask your doctor or pharmacist.

Medicine questions

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4. Possible side effects

Like all medicines, Sodium Iodide (123I) can have side effects, although not everyone gets them.

For all patients: exposure to ionizing radiation should be justified based on the expected medical objective, obtained with the minimum possible dose of radiation received by the patient. Exposure to ionizing radiation is associated with the induction of cancer and the possibility of developing hereditary defects. The probability of these reactions occurring is low due to the low doses of radiation received.

Isolated cases of allergic reactions have been reported without more precise information on frequency and details of such reactions.

If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet.

Reporting of side effects

If you experience side effects, consult your nuclear medicine doctor, even if they are side effects not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.

5. Storage of Sodium Iodide (123I) Curium Pharma Spain 37 MBq/ml injectable solution

Keep out of the reach and sight of children.

Before opening the package for the first time, the product should be stored at a temperature between 15°C and 25°C.

Storage should be carried out in accordance with national regulations on radioactive materials.

The storage period of the vial is 20 hours after the calibration date. The expiration date is indicated on the outside of the package.

Do not use Sodium Iodide (123I) Curium Pharma Spain after the expiration date stated on the package label.

After opening the package for the first time, the storage period is 8 hours when stored between 2-8°C.

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.

6. Package contents and further information

Composition of Sodium Iodide (123I) Curium Pharma Spain

  • The active substance is Sodium Iodide (123I). 1 ml of injectable solution contains 37 MBq of Sodium Iodide (123I) at the calibration date and time
  • The other components are sodium chloride, sodium hydrogencarbonate, and water for injections.

Appearance of the product and package contents

This medicine is presented as an injectable solution. It is supplied in 10 ml glass vials, type I, Ph. Eur., sealed with a bromobutyl rubber stopper coated with Teflon and an aluminum overseal.

A vial contains 1, 2, 5, or 10 ml of injectable solution, corresponding to activities of 37 MBq, 74 MBq, 185 MBq, and 370 MBq at the calibration date and time.

Marketing authorization holder and manufacturer:

Marketing authorization holder:

Curium Pharma Spain S.A.

Avenida Doctor Severo Ochoa, 29

28100, Alcobendas, Madrid

Manufacturer:

Curium Netherlands B.V.

Westerduinweg 3

1755 LE Petten

Netherlands

Date of last revision of this leaflet: March 2016

This information is intended only for healthcare professionals:

The full technical data sheet of Sodium Iodide (123I) Curium Pharma Spain is included as a section at the end of this leaflet, in order to provide doctors or healthcare professionals with scientific information and practical information on the administration and use of this radiopharmaceutical.

Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.es/

Online doctors for SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION

Discuss questions about SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION, including use, safety considerations and prescription review, subject to medical assessment and local regulations.

5.0 (3)
Doctor

Tomasz Grzelewski

Dermatology 21 years exp.

Dr Tomasz Grzelewski is an MD, PhD specialist in allergy, paediatrics, general practice and sports medicine, with a clinical focus on dermatology, endocrinology, allergology and sports-related health. He has more than 20 years of clinical experience and completed his medical training at the Medical University of Łódź, where he defended his PhD thesis with distinction. His doctoral research was recognised by the Polish Society of Allergology for its innovative contribution to the field. Throughout his career, he has gained extensive expertise in diagnosing and managing a wide range of allergic and paediatric conditions, including modern allergen desensitisation techniques.

For five years, Dr Grzelewski served as the Head of two paediatric departments in Poland, managing complex clinical cases and leading multidisciplinary teams. He also worked in medical centres in the United Kingdom, gaining experience across both primary care and specialist environments. With over a decade of telemedicine experience, he has provided online consultations across Europe and is valued for his clear, structured and evidence-based medical guidance.

Dr Grzelewski is actively involved in clinical programmes focused on modern anti-allergic therapies. As a Principal Investigator, he leads research projects on sublingual and oral allergen desensitisation, supporting evidence-based progress in allergy treatment for both children and adults.

In addition to his background in allergology and paediatrics, he completed dermatology studies through the Cambridge Education Group (Royal College of Physicians of Ireland) and a Clinical Endocrinology course at Harvard Medical School. This advanced training enhances his ability to manage skin manifestations of allergies, atopic conditions, urticaria, endocrine-related symptoms and complex immunological reactions.

Patients commonly seek his care for:

  • seasonal and perennial allergies
  • allergic rhinitis and chronic nasal symptoms
  • asthma and breathing difficulties
  • food and medication allergies
  • urticaria, atopic dermatitis and skin reactions
  • recurrent infections in children
  • sports-related health questions
  • general family medicine concerns
Dr Tomasz Grzelewski is known for his clear communication style, structured medical approach and ability to explain treatment options in a concise and accessible way. His multidisciplinary background across allergy, paediatrics, dermatology and endocrinology allows him to provide safe, up-to-date and comprehensive care for patients of all ages.
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Doctor

Anna Biriukova

General medicine 6 years exp.

Dr Anna Biriukova is an internal medicine doctor with clinical experience in cardiology, endocrinology, and gastroenterology. She provides online consultations for adults, offering expert medical support for heart health, hormonal balance, digestive issues, and general internal medicine.

Cardiology – Diagnosis and treatment of:

  • High blood pressure, blood pressure fluctuations, and cardiovascular risk prevention.
  • Chest pain, shortness of breath, arrhythmias (tachycardia, bradycardia, palpitations).
  • Leg swelling, chronic fatigue, reduced exercise tolerance.
  • EKG interpretation, lipid profile evaluation, cardiovascular risk assessment (heart attack, stroke).
  • Post-COVID-19 cardiac monitoring and care.
Endocrinology – Diabetes, thyroid, metabolism:
  • Diagnosis and management of type 1 and type 2 diabetes, and prediabetes.
  • Individual treatment plans including oral medications and insulin therapy.
  • GLP-1 therapy– modern pharmacological treatment for weight management and diabetes control, including drug selection, monitoring, and safety follow-up.
  • Thyroid disorders – hypothyroidism, hyperthyroidism, autoimmune thyroid diseases (Hashimoto’s, Graves’ disease).
  • Metabolic syndrome – obesity, lipid disorders, insulin resistance.
Gastroenterology – Digestive health:
  • Abdominal pain, nausea, heartburn, gastroesophageal reflux (GERD).
  • Stomach and intestinal conditions: gastritis, irritable bowel syndrome (IBS), indigestion.
  • Management of chronic digestive disorders and interpretation of tests (endoscopy, ultrasound, labs).
General internal medicine and preventive care:
  • Respiratory infections – cough, colds, bronchitis.
  • Lab test analysis, therapy adjustments, medication management.
  • Adult vaccinations – planning, contraindications assessment.
  • Cancer prevention – screening strategies and risk assessment.
  • Holistic approach – symptom relief, complication prevention, and quality of life improvement.
Dr Biriukova combines internal medicine with specialist insight, offering clear explanations, personalised treatment plans, and comprehensive care tailored to each patient.
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€60
5.0 (29)
Doctor

Dmytro Horobets

Family medicine 7 years exp.

Dr. Dmytro Horobets is a licensed family medicine physician in Poland, specialising in endocrinology, diabetology, obesity management, gastroenterology, pediatrics, general surgery, and pain medicine. He offers online consultations for adults and children, providing personalised medical support for a wide range of acute and chronic health concerns.

Areas of expertise:

  • Endocrinology: diabetes type 1 and type 2, prediabetes, thyroid disorders, metabolic syndrome, hormonal imbalance.
  • Obesity medicine: structured weight management plans, nutritional counselling, obesity-related health risks.
  • Gastroenterology: acid reflux (GERD), gastritis, irritable bowel syndrome (IBS), liver and biliary conditions.
  • Pediatric care: infections, respiratory symptoms, digestive issues, growth and development monitoring.
  • General surgery support: pre- and post-surgical consultations, wound care, rehabilitation.
  • Pain management: chronic and acute pain, back pain, joint pain, post-traumatic pain syndromes.
  • Cardiovascular health: hypertension, cholesterol control, risk assessment for heart disease.
  • Preventive medicine: regular check-ups, health screenings, long-term management of chronic conditions.

Dr. Horobets combines evidence-based medicine with a patient-centred approach. He carefully evaluates each patient’s medical history and symptoms, offering clear explanations and structured treatment plans adapted to individual needs.

Whether you need help managing diabetes, tackling weight-related health issues, interpreting lab results, or receiving general family medicine support, Dr. Horobets provides professional online care tailored to your specific health goals.

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€60

Frequently Asked Questions

Is a prescription required for SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION?
SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION requires a prescription in Spain. You can check with a doctor online whether this medicine may be appropriate for your situation.
What is the active substance in SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION?
The active ingredient in SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION is sodium iodide (123I). This information helps identify medicines with the same composition but different brand names.
Who manufactures SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION?
SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION is manufactured by Curium Pharma Spain S.A.. Pharmacy brands and packaging may differ depending on the distributor.
Which doctors can assess the use of SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION online?
Doctors such as Family doctors, Psychiatrists, Dermatologists, Cardiologists, Endocrinologists, Gastroenterologists, Pulmonologists, Nephrologists, Rheumatologists, Hematologists, Infectious disease physicians, Allergists, Geriatricians, Paediatricians, Oncologists may assess whether SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION is appropriate, depending on your situation and local regulations. You can book an online consultation to discuss your symptoms and possible next steps.
What are the alternatives to SODIUM IODIDE (123 I) CURIUM PHARMA SPAIN 37 MBq/ml INJECTABLE SOLUTION?
Other medicines with the same active substance (sodium iodide (123I)) include SODIUM IODIDE (123I) GE HEALTHCARE 37 MBq/mL INJECTABLE SOLUTION, MONTEK 10-40 GBq RADIOPHARMACEUTICAL GENERATOR, TEKCIS 2-50 GBq RADIOPHARMACEUTICAL GENERATOR. These may have different brand names or formulations but contain the same therapeutic ingredient. Always consult a doctor before switching or starting a new medicine.
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