Meglumine iotroxate 105mg/ml (Iodine 50mg/ml) solution for infusion 100ml bottles
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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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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.
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: 5 · Randomised trials: 6 · 1987–2024
Showing the 50 most relevant studies, sorted by most relevant.
Meliana Borilli Pereira, B. Sydor, Karla Gabriela Memare, et al.
Nanomedicine, 2021
Jamile Lago, D. Fraga, L. H. Guimarães, et al.
PLOS Neglected Tropical Diseases, 2023
A. Ziegler, C. K. Freeman, C. Fogle, et al.
Equine veterinary journal, 2018
P. Machado, Camila da S. Ribeiro, Jaqueline França‐Costa, et al.
Tropical Medicine & International Health, 2018
R. N. R. Sampaio, Juliana Saboia Fontenele E Silva, Carmen Déa Ribeiro de Paula, et al.
Revista da Sociedade Brasileira de Medicina Tropical, 2019
Dandan Zhang, Yi Wang, Zhihong Meng, et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 2022
D. Kasabalis, M. Chatzis, K. Apostolidis, et al.
Experimental parasitology, 2020
P. Robert, Stefanie Fingerhut, Cécile Factor, et al.
Radiology, 2018
Purpose To compare the long-term brain elimination kinetics and gadolinium species in healthy rats after repeated injections of the contrast agents gadodiamide (a linear contrast agent) or gadoterate (a macrocyclic contrast agent). Materials and Methods Nine-week-old rats received five doses of 2.4 mmol gadolinium per kilogram of body weight over 5 weeks and were followed for 12 months with T1-weighted MRI (n = 140 rats, corresponding to seven time points, two contrast agents, and 10 rats per group). Animals were sacrificed at 1 week, 1 month, and 2, 3, 4, 5, and 12 months after the last injection. Brain and plasma were sampled to determine the total gadolinium concentration by using inductively coupled plasma mass spectrometry (ICP-MS). For the cerebellum, gadolinium speciation analysis was performed after mild extraction at four time points (1 month and 3, 5, and 12 months after the last injection) by using size exclusion chromatography and hydrophilic interaction liquid chromatography, both coupled to ICP-MS. Tissue gadolinium kinetics were fitted to estimate the area under the curves and tissue elimination half-lives over the 12-month injection-free period. Results T1 hyperintensity of the deep cerebellar nuclei was observed only in gadodiamide-treated rats and remained stable from the 1st month after the last injection (the ratio of the signal intensity of the deep cerebellar nuclei to the signal intensity of the brain stem at 1 year: 1.101 ± 0.023 vs 1.037 ± 0.022 before injection, P < .001). Seventy-five percent of the total gadolinium detected after the last injection of gadodiamide (3.25 nmol/g ± 0.30) was retained in the cerebellum at 1 year (2.45 nmol/g ± 0.35), with binding of soluble gadolinium to macromolecules. No T1 hyperintensity was observed with gadoterate, consistent with a rapid, time-dependent washout of the intact gadolinium chelate down to background levels (0.07 nmol/g ± 0.03). Conclusion After repeated administration of gadodiamide, a large portion of gadolinium was retained in the brain, with binding of soluble gadolinium to macromolecules. After repeated injection of gadoterate, only traces of the intact chelated gadolinium were observed with time-dependent clearance. Online supplemental material is available for this article.
Abstract licence: CC BY
S. H. Carvalho, F. Frézard, N. Pereira, et al.
Tropical Medicine & International Health, 2019
E. de Kerviler, K. Maravilla, J. Meder, et al.
Investigative Radiology, 2016
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.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.