IOMERON 200 MG IODO/ML INJECTABLE SOLUTION

Introduction

PACKAGE LEAFLET: INFORMATION FOR THE USER

Iomeron 200 mg Iodo/ml injectable solution

Iomeprol

Read all of this leaflet carefully before you start using this medicine because it contains important information for you.

• 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 only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
• If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

Contents of the pack:

1. What Iomeron 200 mg Iodo/ml injectable solution is and what it is used for
2. What you need to know before you use Iomeron 200 mg Iodo/ml injectable solution
3. How to use Iomeron 200 mg Iodo/ml injectable solution
4. Possible side effects
5. Storage of Iomeron 200 mg Iodo/ml injectable solution
6. Contents of the pack and other information

1. What Iomeron 200 mg Iodo/ml injectable solution is and what it is used for

This medicinal product is for diagnostic use only.

Iomeron belongs to a group of medicines called low-osmolar, water-soluble, nephrotropic X-ray contrast media.

Iomeron is used to improve the visualization of different body areas by means of certain radiological techniques. In adults, it is used for computed tomography (CT) of the head and body, cavernosography, peripheral phlebography, digital subtraction phlebography, digital subtraction angiography, endoscopic retrograde cholangiopancreatography (ERCP), retrograde cholangiography, arthrography, hysterosalpingography, retrograde ureterography, retrograde pyelography, and myelography. In children from 0 to 18 years for computed tomography (CT) of the head and body and digital subtraction angiography.

2. What you need to know before you use Iomeron 200 mg Iodo/ml injectable solution

Do not use Iomeron 200 mg Iodo/ml injectable solution

• If you are allergic to iomeprol or any of the other ingredients of this medicinal product (listed in section 6).
• If you have Waldenström's paraproteinemia.
• If you have severe hepatic or renal disorders.
• If you have multiple myeloma.

Investigations of female genitals are contraindicated in case of suspected or confirmed pregnancy and in case of acute inflammation.

Immediate repetition of Iomeron administration if a technical failure occurs is contraindicated in myelography.

Warnings and precautions

• Before starting the examination, you should be adequately hydrated and should avoid eating food for two hours before the examination.
• In states of anxiety and pain, as they may intensify adverse reactions related to the contrast medium. In these cases, a sedative may be administered.
• If used in the elderly.
• If you have asthma.
• If you have ever developed a severe skin rash or peeling of the skin, blisters, and/or sores in the mouth after receiving iodinated contrast media.
• If you have hay fever, urticaria, or food allergies, as patients with a history of allergy are more susceptible to suffering adverse reactions to iodinated contrast media.
• If you have hyperthyroidism and/or nodular goiter, as the use of non-ionic contrast media may trigger thyroid crises.
• If you have renal insufficiency.
• If you have diabetes mellitus; these patients may develop lactic acidosis if they are being treated with biguanides (e.g., metformin). As a precaution, in patients with moderate renal insufficiency, biguanides should be discontinued at the time of or 48 hours before the examination with a contrast medium and reinstated only after it has been verified that renal function has recovered.
• If you have acute pancreatitis and are undergoing an ERCP procedure to explore your pancreas.
• If you have pheochromocytoma (a type of tumor), as hypertensive crises may occur after using the contrast medium intravascularly. Premedication with alpha-adrenergic blockers is recommended.
• If you have sickle cell anemia (a type of anemia), as contrast media may worsen your condition.
• If you have myasthenia gravis (a disease that causes muscle weakness), as your condition may worsen.
• In case of severe cardiovascular disease, especially if you suffer from heart failure, coronary arteriopathy (disease of the heart's blood vessels), pulmonary hypertension, and coronary valvulopathy.
• When you have central nervous system disorders, as convulsive crises may occur.
• In case of alcoholism and drug addiction.

Fluoroscopy is recommended to minimize extravasation during injection.

You may experience a short-term brain disorder, called encephalopathy, during or shortly after the imaging procedure. Inform your doctor immediately if you notice any symptoms related to this condition, described in section 4.

Thyroid disorders have been observed after Iomeron administration in both children and adults. Infants may also be exposed through the mother during pregnancy. Your doctor may need to perform thyroid function tests before and/or after Iomeron administration.

Severe skin reactions, including Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), acute generalized exanthematous pustulosis (AGEP), and drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported in association with the use of Iomeron. Go to your doctor immediately if you observe any symptoms related to these severe skin reactions described in section 4.

Consult your doctor before starting to use Iomeron 200 mg Iodo/ml injectable solution.

Children

Children under one year of age, especially neonates, are particularly susceptible to electrolyte imbalances and hemodynamic alterations.

Other medicines and Iomeron 200 mg Iodo/ml injectable solution

Tell your doctor if you are using, have recently used, or might use any other medicines.

Do not interrupt treatment with anticonvulsant drugs and ensure their administration in optimal doses.

In patients treated with immunomodulatory drugs, such as Interleukin-2, allergic reactions to contrast media are more frequent and may manifest as late reactions.

This medicinal product must not be mixed with other medicines.

Interference with laboratory tests:

Iodinated contrast media may interfere with thyroid function studies, as the thyroid's ability to capture radioisotopes will be reduced for periods of two weeks or more.

High concentrations of contrast media in plasma and urine may alter the results of laboratory tests for bilirubin, proteins, and inorganic substances (e.g., iron, copper, calcium, phosphate).

Using Iomeron 200 mg Iodo/ml injectable solution with food and drinks

If there are no specific instructions from your doctor, you can follow a normal diet on the day of the examination. Confirm adequate fluid intake. However, you should avoid eating food for two hours before the examination.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor before using this medicinal product.

Pregnancy

You should inform your doctor if you are pregnant or think you may be pregnant.

As with other non-ionic contrast media, there are no controlled studies in pregnant women that confirm the safety of the product in humans. Since, whenever possible, exposure to radiation should be avoided during pregnancy, the risk/benefit ratio of any X-ray examination, with or without contrast media, should be carefully evaluated.

If you are pregnant and have received Iomeron during pregnancy, it is recommended to analyze the thyroid function of your newborn.

Breastfeeding

Contrast media are barely excreted in breast milk, and the possibility of the infant suffering any harm is remote.

Driving and using machines

No effects on the ability to drive and use machines have been observed.

3. How to use Iomeron 200 mg Iodo/ml injectable solution

This medicinal product will always be administered by qualified and properly trained personnel, in hospitals or clinics that have the necessary personnel and equipment.

The dose that will be administered to you will vary depending on the type of examination, age, body weight, cardiac output, and general condition you present, as well as the technique used.

If you use more Iomeron 200 mg Iodo/ml injectable solution than you should

Overdose can cause severe adverse reactions, mainly through effects on the cardiovascular and pulmonary systems.

Treatment of an overdose is aimed at maintaining all vital functions and involves the rapid initiation of symptomatic therapy. Iomeron can be eliminated from the body through dialysis.

In case of overdose or accidental ingestion, consult your doctor or pharmacist or call the Toxicology Information Service, telephone 91 562 04 20, indicating the medicinal product and the amount ingested.

If you have any doubts about the use of this product, consult your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Generally, side effects are mild to moderate and are of a transient nature. However, severe and potentially life-threatening reactions have been reported, sometimes with a fatal outcome. In most cases, reactions occur within minutes of administration, although they may sometimes appear later.

Inform your doctor immediately if you suffer from any of the following symptoms: sudden wheezing, difficulty breathing, swelling of the eyelids, face, or lips, skin rash, or itching that affects the whole body.

The following side effects have been reported:

Intravascular administration

Common(may affect up to 1 in 10 people):

• feeling of heat

Uncommon(may affect up to 1 in 100 people):

• headache
• dizziness
• increased blood pressure
• difficulty breathing
• nausea, vomiting
• flushing, urticaria, itching
• chest pain, heat, and pain at the injection site

Rare(may affect up to 1 in 1,000 people)

• fainting
• slow or fast heart rate
• decreased blood pressure
• skin rash
• back pain
• asthenia, stiffness, fever
• increased creatinine in blood

Frequency not known(cannot be estimated from the available data):

• Contact a doctor as soon as possible if you experience a severe skin reaction, such as:

• blisters, peeling of the skin, ulcers in the mouth, throat, nose, genitals, and eyes. These severe skin reactions may be preceded by fever and flu-like symptoms (Stevens-Johnson syndrome, toxic epidermal necrolysis).
• a red and scaly rash with bumps under the skin and blisters, accompanied by fever. The symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).
• a widespread rash, high body temperature, and swollen lymph nodes (DRESS or drug hypersensitivity syndrome)

• anxiety, hyperkinetic syndrome (increased motor activity), confusion
• allergic reactions
• hyperthyroidism
• loss of appetite (anorexia)
• altered taste, difficulty speaking, disease affecting brain function, cerebral edema (fluid in the brain), transient ischemic attacks (TIAs) with few or no sequelae, memory loss, somnolence, altered sensitivity (tingling, itching), stroke, loss of consciousness, tremors, coma, convulsions, altered sense of smell
• brain disorder (encephalopathy) with symptoms that include headache, vision difficulties, loss of vision, confusion, convulsions, loss of coordination, loss of movement in a part of the body, speech problems, and loss of consciousness.
• temporary blindness, vision impairment, conjunctivitis, increased tearing, photopsia (seeing lights)
• myocardial infarction, cardiac arrest, chest tightness, arrhythmias, angina pectoris, heart failure, formation of blood clots in the coronary arteries (after catheter insertion), irregular heartbeat, conduction disorders
• flushing, shock (severe drop in blood pressure), pallor, fatigue, cool and moist skin, reduced consciousness) caused by sudden and severe dilation of blood vessels, blue discoloration of the skin and mucous membranes, blood clots, vasospasm, and consequent ischemia.
• circulatory failure (circulatory collapse)
• coronary artery obstruction (after catheter insertion)
• respiratory arrest, cough, acute respiratory distress syndrome (ARDS), wheezing, asthma attacks, fluid accumulation in the throat, fluid in the lungs, inflammation of the nasal mucosa characterized by a stuffy nose, sneezing, and discharge (rhinitis), hoarseness (dysphonia), insufficient oxygen supply to tissues (hypoxia), sore throat and larynx, sudden constriction of the airways (bronchospasm)
• intestinal incontinence, diarrhea, abdominal pain, excessive salivation, difficulty swallowing, pancreatitis, salivary gland enlargement, intestinal obstruction
• severe hypersensitivity reactions, characterized by symptoms such as increased sweat production, dizziness, itching, pulsating headache, throat tightness, inflammation of the mouth and throat mucosa, which can make breathing difficult
• eczema, skin rash, increased sweat production, sudden fluid accumulation in the skin and mucous membranes (e.g., throat or tongue), possibly with difficulty breathing and/or itching and skin rash (angioedema), appearance of circular blisters on the skin (whose center is usually paler) (erythema multiforme)
• joint pain, muscle stiffness
• acute renal failure, urinary incontinence, urine abnormalities, decreased urine production
• general feeling of illness (malaise), chills, localized feeling of cold, thirst, reaction at the injection site, hematoma at the injection site
• blood disorders (decreased platelet count) accompanied by bruising and a tendency to bleed (thrombocytopenia)
• hemolytic anemia (abnormal decrease in red blood cells that can cause fatigue, rapid heart rate, and difficulty breathing)

Transient hypothyroidism may occur in children under 3 years of age.

In some cases, alterations are detected during medical examinations (blood tests, cardiac and hepatic function tests).

Administration in the cerebrospinal fluid

Very common(more than 1 in 10 people):

• headache

Common(more than 1 in 100 people and less than 1 in 10 people):

• dizziness
• increased blood pressure
• nausea, vomiting
• back pain, pain in the limbs
• reaction at the injection site

Uncommon(more than 1 in 1,000 people and less than 1 in 100 people):

• loss of consciousness
• altered sensitivity
• somnolence
• decreased blood pressure
• flushing
• muscle stiffness
• neck pain
• feeling of heat
• chest pain
• fever

Frequency not known(cannot be estimated from the available data):

• allergic reactions
• epilepsy
• skin rash
• general feeling of illness
• brain disorder (encephalopathy) with symptoms that include headache, vision difficulties, loss of vision, confusion, convulsions, loss of coordination, loss of movement in a part of the body, speech problems, and loss of consciousness

Administration in body cavities

• allergic reactions
• alteration of blood tests (after pancreas examinations)
• as with other iodinated contrast media, pelvic pain and general discomfort may occur after an examination of the cervix, fallopian tubes, and ovaries.

Consult your doctor if you experience severe symptoms or allergic reactions (hypersensitivity), or if the symptoms persist for long periods of time.

The safety profile of iomeprol is similar in adults and children for all routes of administration.

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 through the Spanish Pharmacovigilance System for Human Use http://www.notificaRam.es. By reporting side effects, you can help provide more information on the safety of this medicinal product.

5. Storage of Iomeron 200 mg Iodo/ml injectable solution

Keep this medication out of sight and reach of children.

Store the vial in the outer packaging to protect it from light.

Although the sensitivity of iomeprol to X-rays is low, it is advisable to store the product out of reach of ionizing radiation.

Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.

Medicines should not be disposed of via wastewater or household waste. In case of doubt, ask your pharmacist how to dispose of packaging and medications that are no longer needed. This will help protect the environment.

6. Container Content and Additional Information

Composition of Iomeron 200 mg Iodo/ml Injectable Solution

• The active ingredient is iomeprol. 1 ml of injectable solution contains 408.2 mg of iomeprol, equivalent to 200 mg of iodine.
• The other components are trometamol, hydrochloric acid for pH adjustment, and water for injectable preparations c.s.p.

Product Appearance and Container Content

Iomeron is packaged in glass vials closed with halobutyl stoppers and an aluminum cap.

Single-dose vials of 50 ml, 100 ml, and 200 ml.

Only some package sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Marketing Authorization Holder

Bracco Imaging s.p.a.

Via E. Folli 50

20134 (Milan - Italy)

Manufacturer

Patheon Italia s.p.a.

2nd Left Traversal Via Morolense, 5

03013 Ferentino (Italy)

Bracco Imaging S.p.A.

Bioindustry Park - Via Ribes, 5

10010 Colleretto Giacosa (TO) (Italy)

You can request more information about this medication by contacting the local representative of the marketing authorization holder:

Laboratorios Farmacéuticos ROVI, S.A.

Julián Camarillo, 35

28037 Madrid

Tel: 913756230

Date of the last revision of this prospectus:September 2023

Detailed and updated information about 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 healthcare professionals:

Iomeron 200 mg Iodo/ml is an injectable solution for intravenous, intraarterial, intracavernous, intracolangiopancreatic, intraarticular, intrauterine, intravesical, and intrathecal administration.

Whenever possible, intravascular administration of contrast media should be performed with the patient lying down. The patient should be kept under observation for at least 30 minutes after administration.

Before use, the solution must be visually inspected. Only solutions without visible signs of deterioration or particles will be used.

The disposal of unused medication and all materials that have come into contact with it will be carried out in accordance with local regulations.

Precautions

• Regarding the patient:

Hydration- Any severe alteration of the hydroelectrolytic balance must be corrected. Before the medical examination, ensure adequate hydration, especially in patients with severe functional impairment of the kidneys, multiple myeloma or other paraproteinemias, sickle cell anemia, diabetes mellitus, polyuria, oliguria, hyperuricemia, as well as in neonates, children, and elderly patients.

Dietary Suggestions- If there are no specific instructions from the doctor, a normal diet can be followed. Confirm adequate fluid intake. However, the patient should abstain from eating food in the two hours prior to the examination.

Hypersensitivity- In patients with a predisposition to allergies, with known hypersensitivity to iodinated contrast media and with a history of asthma, premedication with antihistamines and/or corticosteroids may be considered to prevent possible anaphylactoid reactions.

Severe Cutaneous Adverse Reactions- Severe cutaneous adverse reactions (SCARs), including Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), acute generalized exanthematous pustulosis (AGEP), and drug reaction with eosinophilia and systemic symptoms (DRESS), which can be fatal or potentially fatal, have been reported in patients who received iodinated contrast media by intravascular route. At the time of administration, patients should be warned about the signs and symptoms, and closely monitored for the appearance of skin reactions. If signs and symptoms suggesting the appearance of these reactions occur, the administration of Iomeron should be suspended immediately. If the patient has developed a severe reaction such as SJS, TEN, AGEP, or DRESS with the use of Iomeron, Iomeron should not be administered to that patient again at any time.

Anxiety- States of excitement, anxiety, and pain can cause side effects or intensify reactions related to the contrast medium. In these cases, a sedative can be administered.

Concomitant Treatments- Consider interrupting treatment with drugs that reduce the convulsive threshold up to 24 hours after the intervention, in case of intrathecal use, and in patients with disorders of the blood-brain barrier (see "Neurological symptoms").

• Regarding the procedure:

Coagulation, Catheterization- A property of non-ionic contrast media is the minimal interference with physiological functions. As a consequence, non-ionic contrast media have, in vitro, a lower anticoagulant activity than ionic contrast media. The medical and paramedical personnel performing vascular catheterization should be informed of this and should pay particular attention to the angiographic technique. Non-ionic contrast media should not come into contact with blood in the syringe, and intravascular catheters should be frequently cleaned to minimize the risk of thromboembolism related to the procedure.

Patient Observation- Whenever possible, intravascular administration of contrast media should be performed with the patient lying down. The patient should be kept under observation for at least 30 minutes after administration.

Sensitivity Test- A sensitivity test is practically useless, since the occurrence of severe or fatal reactions due to contrast media cannot be predicted with such a test.

Risk of Inflammation and Extravasation- Caution is recommended during the injection of contrast media to avoid extravasation.

Warnings

• Common to all forms of administration

Considering the possible serious side effects, the use of iodinated contrast media should be limited to specific needs for contrastographic examinations.

This need should be considered according to the patient's clinical conditions, especially in relation to cardiovascular, urinary, and hepatobiliary pathologies.

Contrast media for angiographic examinations should be used in hospitals or clinics with competent personnel and necessary equipment for intensive care in case of emergency. In centers where more common diagnostic tests are performed that require the use of iodinated contrast media, it is necessary that the radiology services where these tests are performed have therapeutic measures and resuscitation equipment that experience has confirmed to be suitable (Ambu bag, oxygen, antihistamines, vasoconstrictors, etc.).

Use in:

Pediatric Population- Children under one year of age, especially neonates, are particularly susceptible to electrolyte imbalances and hemodynamic alterations. Attention should be paid to the doses to be used, the procedure technique, and the patient's condition. Hypothyroidism or transient suppression of the thyroid may be observed after exposure to iodinated contrast media. Special attention should be paid to pediatric patients under 3 years of age, as an episode of low thyroid activity during the first years of life can be detrimental to motor, auditory, and cognitive development and may require temporary replacement treatment with T4. The incidence of hypothyroidism in patients under 3 years of age exposed to iodinated contrast media has been reported between 1.3% and 15%, depending on the age of the subjects and the dose of the iodinated contrast medium, and is more frequently observed in neonates and premature infants. Thyroid function should be evaluated in all pediatric patients under 3 years of age after exposure to iodinated contrast media. If hypothyroidism is detected, the need for treatment should be considered, and thyroid function should be monitored until it normalizes.

Elderly- Elderly patients should be considered at special risk for reactions due to excessive dosing of the contrast medium. The frequent association of neurological disorders and vascular pathologies constitutes an aggravating factor.

Patients with Particular Pathological Conditions

• Hypersensitivity to iodinated contrast media- Hypersensitivity or previous reactions to iodinated contrast media also increase the risk of recurrence of a severe reaction, even with non-ionic contrast media.
• Allergic predisposition- It is known that adverse reactions to iodinated contrast media are more common in patients with a history of allergy: hay fever, urticaria, and food allergies.
• Asthmatic patients- Patients taking beta-adrenergic blockers, in particular asthmatic patients, may have a lower threshold for bronchospasm and a lower response to treatment with beta-agonists and adrenaline, which may require the use of higher doses.
• Thyroid function and thyroid function tests- Iodinated contrast media may contain small amounts of free inorganic iodide that could have effects on thyroid function. These effects are more evident in patients with latent or overt hyperthyroidism, or goiter. Hyperthyroidism or even thyrotoxic crisis has been reported after the administration of iodinated contrast media.

• Intraarterial and Intravenous Administration

Use in Patients with Special Pathological Conditions

Renal Impairment- In patients with compromised renal function, the administration of contrast media can cause episodes of renal failure. Preventive measures include: identifying high-risk patients; ensuring adequate hydration before the administration of the contrast medium, preferably maintaining intravenous infusion before, during the procedure, and until the contrast medium has been eliminated by the kidneys; avoiding, if possible, the administration of nephrotoxic drugs and subjecting the patient to major surgical interventions or procedures such as renal angioplasty until the contrast medium has been completely eliminated; postponing a new examination with contrast medium until renal function returns to pre-examination levels. Patients on dialysis can receive contrast media, such as iomeprol, that are easily dialyzable.

Diabetes Mellitus- The presence of renal damage in diabetic patients is one of the factors that predisposes to renal dysfunction as a consequence of the administration of contrast media.

Renal impairment can cause lactic acidosis in diabetic patients with renal damage treated with biguanides (metformin). To prevent this, treatment with biguanides should be suspended in the following cases: before intraarterial administration of a contrast medium with first-pass renal exposure, in patients with eGFR less than 30 ml/min/1.73 m2 who receive a contrast medium intravenously or a contrast medium intraarterially with second-pass renal exposure, or in patients with acute kidney injury, and should only be resumed after 48 hours, provided that renal function has not changed significantly.

CPER- The risk associated with CPER procedures in patients with acute, obstructive, or non-obstructive pancreatitis should be carefully evaluated with respect to the expected benefits.

Pheochromocytoma- These patients can develop severe hypertensive crises (rarely uncontrollable) after using intravascular contrast medium during radiological procedures.

In patients with pheochromocytoma, premedication with alpha-receptor blockers is recommended due to the risk of hypertensive crises.

Myasthenia Gravis- The administration of iodinated contrast media can worsen the signs and symptoms of myasthenia.

Cardiac Disease and Pulmonary Hypertension- There is a high risk of severe reactions in patients with severe cardiovascular disease, particularly those with heart failure and coronary arteriopathy. The intravascular injection of contrast media can cause pulmonary edema in patients with overt or incipient cardiac decompensation, while the administration of the contrast medium in cases of pulmonary hypertension and valvulopathy can favor hemodynamic alterations. The appearance of signs of ischemia on the ECG and severe arrhythmias is more common in older patients and those with pre-existing cardiopathy: their frequency and severity seem to be related to the severity of the cardiac pathology.

Neurological Symptoms- Particular attention should be paid when administering a contrast medium to patients with acute cerebral infarction, intracranial hemorrhage, and those with alterations of the blood-brain barrier, cerebral edema, or acute demyelination. The presence of intracranial tumors or metastases and a history of epilepsy can increase the probability of seizure onset. The administration of contrast media can exacerbate neurological symptoms due to degenerative, ischemic, inflammatory, or neoplastic cerebrovascular pathologies. These patients have a higher risk of transient neurological complications. Intravascular injections of contrast media can cause angiospasm and episodes of cerebral ischemia.

Contrast-Induced Encephalopathy– Contrast-induced encephalopathy has been reported with the use of iomeprol.

Contrast-induced encephalopathy can manifest with symptoms and signs of neurological dysfunction such as headache, visual disturbances, cortical blindness, confusion, seizures, loss of coordination, hemiparesis, aphasia, loss of consciousness, coma, and cerebral edema in the minutes to hours after the administration of iomeprol, and usually disappears within a few days.

The product should be used with caution in patients with diseases that affect the integrity of the blood-brain barrier (BBB), which could cause greater permeability of the contrast medium through the BBB and increase the risk of encephalopathy. If contrast-induced encephalopathy is suspected, the administration of iomeprol should be suspended, and adequate medical monitoring should be initiated.

Alcoholism- It has been demonstrated, and

Experimentally and clinically, it has been shown that acute or chronic alcoholism increases the permeability of the blood-brain barrier. This facilitates the passage of iodinated agents into the brain tissue, which can produce central nervous system disorders. A possible reduction in the epileptic threshold in alcoholics should be taken into account.

Drug addiction- Drug-addicted patients require special attention due to the possible reduction in the convulsive threshold.

It is recommended to perform fluoroscopy to minimize extravasation during injection.

Overdose

In the event that the responsible physician diagnoses an accidental intravascular overdose of the contrast medium, the patient's hydration and electrolyte balance should be monitored and corrected if necessary. In this situation, renal function should be monitored for at least three days.

In the event of an accidental intrathecal overdose, the patient should be carefully monitored for at least 24 hours to detect signs and symptoms of central nervous system disorders. These signs may include: increased hyperreflexia or tonic-clonic spasms, and even generalized convulsions, hyperthermia, stupor, and respiratory depression.