Samarium [Sm-153] lexidronam pentasodium 3.4GBq/2.6ml solution for injection vials
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1 branded products available
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View all licensed products for Samarium [Sm-153] lexidronam pentasodium on the MHRA register
Quadramet [Sm-153] 3.4GBq/2.6ml solution for injection vials
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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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 all 33 studies.
Reviews & meta-analyses: 4 · 1968–2026
Showing all 33 studies, sorted by most relevant.
Gacon R, Chapuis R, Fabris-Davet L, et al.
2026
BackgroundDrug interactions with diagnostic radiopharmaceuticals are well recognized, as they can modify biodistribution and lead to false or misleading diagnostic results. However, little is known about such interactions in the field of therapeutic radiopharmaceuticals, despite their rapid expansion-particularly with targeted radionuclide therapies such as Radioligand Therapy (RLT). This review aims, for the first time, to systematically compile and analyze available data on drug interactions involving therapeutic radiopharmaceuticals, in order to support safer and more effective patient care.Main bodyEighty-three articles investigating drug interactions with [177Lu]Lu-oxodotreotide (Lutathera®), [177Lu]Lu-vipivotide tetraxetan (Pluvicto®), [131I]INa, [131I]I-meta-iodobenzylguanidine ([131I]I-MIBG), [223Ra]RaCl2 (Xofigo®), [90Y]Y-ibritumomab tiuxetan (Zevalin®) or [153Sm]Sm-lexidronam pentasodium (Quadramet®) were included. These studies reported 133 drug interactions, 69% of which were not mentioned in the corresponding summaries of product characteristics. Interactions could be beneficial (e.g., reducing renal toxicity) or harmful (e.g., decreasing therapeutic efficacy or potentiating toxicity). Three interactions involved complementary and alternative medicines (quercetin, Ginkgo biloba and ouabain). Overall, the evidence level for reported interactions was low: 88% were classified as level 3 or 4 according to the Centre for Evidence-Based Medicine (CEBM) scale.ConclusionDrug interactions with therapeutic radiopharmaceuticals remain underreported, yet they may have significant clinical consequences. Clinical radiopharmacy plays a key role in detecting and preventing these interactions. Radiopharmacists, through their expertise, can identify potential interactions, influence therapeutic decisions, and positively impact patient management. Their involvement throughout the care pathway is essential to ensure the safe and effective use of these innovative therapies. Nuclear medicine physicians should also be aware that such interactions can alter biodistribution, compromise therapeutic efficacy, and increase the risk of adverse effects.
Abstract licence: CC BY-NC-ND
Christian Pin, Danielle Briot, Chantal Bassin, et al.
Analytica Chimica Acta, 1994
A. Serafini
Cancer, 2000
O. Sartor, R. Reid, D. Bushnell, et al.
Cancer, 2007
M. Jain, S. Barhate
Asian Journal of Pharmaceutical Research, 2020
A. Serafini
The quarterly journal of nuclear medicine : official publication of the Italian Association of Nuclear Medicine (AIMN) [and] the International Association of Radiopharmacology, 2001
M. Morris, N. Pandit-Taskar, J. Carrasquillo, et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2009
O. Sartor
Reviews in urology, 2004
S. Tu, P. Mathew, F. Wong, et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2009
Tomitsugu Taketatsu, Atsuko Sato
Analytica Chimica Acta, 1979
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.