Iomeprol 71.44% (Iodine 350mg/ml) solution for injection 100ml bottles
Requires a prescription from a doctor or prescriber
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Suspected adverse reactions reported for Iomeprol
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Suspected adverse reactions reported for Iomeprol
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
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Iomeron 350 solution for injection 100ml bottles
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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Codes for healthcare professionals and prescribing systems
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 1 · Randomised trials: 7 · Trials: 1 · 1994–2026
Showing the 50 most relevant studies, sorted by most relevant.
Wei Y, Jiang X, Hibberd M, et al.
2025
- Contrast Media
- Drug-Related Side Effects and Adverse Reactions
- Iohexol
ObjectivesThis systematic review and meta-analysis aimed to assess and compare acute adverse reactions (AAR) rates among non-ionic low-osmolar contrast media (LOCM), examining administration routes and severity-specific impact on AAR rates.Materials and methodsA PubMed and Cochrane Library search identified studies published between January 1989 and March 2024. Inclusion criteria focused on studies with > 100 adult patients who received intra-arterial or intravenous LOCM (iobitridol, iohexol, iomeprol, iopamidol, iopromide, and ioversol). Duplicate reports and studies with insufficient information were excluded. Data extraction and quality assessment followed PRISMA guidelines and the Newcastle Ottawa Scale. Statistical analyses were performed using R software, including random effects, meta-regression, and sub-group analysis.ResultsAfter excluding duplicates and non-compliant studies, 32 peer-reviewed articles of initially 6701 identified studies, were included in the final analysis. The pooled overall AAR rate was 0.73%, with ioversol showing the lowest rate (0.34%). From all studies, pooled rates (random effects model) of moderate and severe AARs were 0.10% and 0.014% (p ConclusionAAR rates were low but indicated significant differences between LOCM; iohexol and ioversol demonstrated the overall most favorable safety profiles.Key pointsQuestion Knowledge about AAR is crucial for patient safety, but comprehensive data on the safety profiles of non-ionic LOCM is lacking. Findings Ioversol showed the lowest overall AAR rate; iohexol demonstrated the lowest moderate/severe AAR. Study design, LOCM type, and injection route influenced AAR rates. Clinical relevance This meta-analysis provides evidence for differences in non-ionic LOCM safety profiles, particularly for moderate and severe AARs. These can guide clinicians in selecting contrast agents, aiming to further reduce risks, and improve patient safety in diagnostic imaging.
Abstract licence: CC BY
on behalf of the X-ACT Study Group, Stephan Achenbach, Jean‐François Paul, et al.
European Radiology, 2016
- Computed Tomography Angiography
- Calcinosis
- Contrast Media
Rainer Schräder, Ingo Esch, R. Ensslen, et al.
Journal of the American College of Cardiology, 1999
- Acute Disease
- Contrast Media
- Coronary Thrombosis
S. Achenbach, J. Paul, F. Laurent, et al.
European Radiology, 2016
Christian Loewe, Christoph R. Becker, Riccardo Berletti, et al.
European Radiology, 2009
- Angiography
- Aorta, Abdominal
- Contrast Media
Henrik S. Thomsen, Sameh K. Morcos, Christiane M. Erley, et al.
Investigative Radiology, 2008
Kunadian Vijayalakshmi, Babu Kunadian, Robert A. Wright, et al.
European Journal of Radiology, 2006
- Bradycardia
- Contrast Media
- Electrocardiography
J.R. Harding, M. Bertazzoli, Alberto Spinazzi
European Journal of Radiology, 1994
- Contrast Media
- Drug Tolerance
- Injections, Intravenous
J.R. Harding, M. Bertazzoli, Alberto Spinazzi
British Journal of Radiology, 1995
- Iohexol
- Iopamidol
- Urography
Lin X, Yang J, Weng L, et al.
2023
- Anaphylaxis
- Iodine Compounds
- Iohexol
BackgroundA comparative hypersensitivity risk profile of frequently used iodinated contrast media (ICM) may be required for their safer use.ObjectiveTo explore the association between hypersensitivity reactions (HSRs) and specific ICM and characterize the spectrum of ICM-related HSRs.MethodsWe performed a disproportionality analysis and proportionality test to assess the safety profile of ICM-related HSRs and compare the frequency ratio of specific HSRs in diverse age, sex, and country subgroups. We used reports downloaded from the US Food and Drug Administration Adverse Event Reporting System and data on the national use of individual ICM for this analysis.ResultsA total of 11,343,365 adverse event reports were collected from the first quarter of 2013 to the first quarter of 2021, among which 5,432 cases were identified as ICM-induced HSRs. All of the studied ICMs were associated with overreporting frequencies of HSRs, in which iomeprol showed the highest reporting odds ratio (ROR) of 24.75 (95% CI, 19.61-31.24). Iopromide (ROR = 22.29; 95% CI, 20.18-24.62) and ioversol (ROR = 20.85; 95% CI, 18.54-23.44) were more likely to cause angioedema than other ICMs, particularly in the group aged 45 to 64 years. Iomeprol was associated with the largest disproportionality for severe cutaneous adverse reactions (ROR = 127.90; 95% CI, 103.32-159.88), whereas iodixanol exhibited maximal incidence when total use cases were considered. Regarding anaphylactic shock, iopamidol presented the highest disproportionality (ROR = 31.11; 95% CI, 27.15-35.65), especially in males or seniors aged greater than 65 years, whereas iopromide resulted in the maximum frequency in China and the United States.ConclusionsDifferent ICMs exhibited diverse profiles regarding HSRs, which could be further affected by age, sex, or geographic area. Prospective studies are required for patient safety.
Abstract licence: CC BY-NC-ND
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
Not available
Mechanism
Iomeprol is a radiographic iodinated contrast agent that opacifies the vessels a…
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
250 mg
[L52260]…
Half-life
[L52260]
Protein binding
[A265090][L52260]
Volume of distribution
[L52260]
In rats, iomeprol was shown to cross the placenta and be excreted into breast milk.
[A265090]…
Metabolism
[A265090][L52260]
Elimination
90%
[A265090][L52260]
Clearance
[L52260]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
- Cerebral arteriography, including intra-arterial digital subtraction angiography (IA-DSA), in adults and pediatric patients
- Visceral and peripheral arteriography and aortography, including IA-DSA, in adults and pediatric patients
- Coronary arteriography and cardiac ventriculography in adults
- Radiographic evaluation of cardiac chambers and related arteries in pediatric patients
Intravenous iomeprol is indicated for:[L52260]
- Computed tomography (CT) of the head and body in adults and pediatric patients
- CT angiography of intracranial, visceral, and lower extremity arteries in adults and pediatric patients
- Coronary CT angiography in adults and pediatric patients
- CT urography in adults and pediatric patients
Known interactions with other medications. Always consult a healthcare professional.
Showing 10 of 10 interactions
[L52510]
The adverse effects of overdosage are life-threatening and affect mainly the pulmonary and cardiovascular systems. Treatment of an overdosage is directed toward the support of all vital functions and prompt institution of symptomatic therapy. Iomeprol can be removed by dialysis.
[L52260]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L52260]
[L52260]
[A265090][L52260]
[L52260]
In rats, iomeprol was shown to cross the placenta and be excreted into breast milk.
[A265090]
[A265090][L52260]
[A265090][L52260]
[L52260]
ATC V08AB10
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Iomeprol
DrugBank citations
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q6062808), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.