Magnesium carbonate mixture aromatic
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MHRA alerts for Magnesium carbonate + Sodium bicarbonate
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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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2 branded products available
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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Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(1)
Source: National Institute for Health and Care Excellence (NICE). 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. 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: 4 · Randomised trials: 2 · 1962–2026
Showing the 50 most relevant studies, sorted by most relevant.
Brian H. Rowe, Jennifer A. Bretzlaff, Chris Bourdon, et al.
Annals of Emergency Medicine, 2000
Badura D, Lorch A, Urgibl-Bauer A, et al.
2026
- Cattle Diseases
- Diarrhea
- Sodium Bicarbonate
G. Marion
Geochimica et Cosmochimica Acta, 2001
Dom A. Terrone, Brian K. Rinehart, Edra S. Kimmel, et al.
American Journal of Obstetrics and Gynecology, 2000
D.R. Laver, T.M. Baynes, A.F. Dulhunty
Journal of Membrane Biology, 1997
Suresh Kumar Gupta, Vijay Kumar
Journal of Soil Salinity and Water Quality, 2024
Nguyen H, Dewitte C, Jin F, et al.
2026
MgO-based cements hold promises as alternatives to Portland cement with radically reduced carbon footprint. MgO plays a centric role in the reaction and formation of these cements. This review is a part of RILEM TC-311 MBC where we discussed the current understanding about the behaviors of MgO in magnesium carbonate (MC) and magnesium silicate (MS) cements. In addition, we reviewed practices in characterizing MgO and available processes to produce MgO in industrial scale. There are several unexpected and unexplained phenomena which likely link to the characteristics of MgO in both MC and MS cements. This distinguishes the MgO-cements from Portland cement and eventually several practices and know-how commonly used in cement research are not applicable and need further insights. Furthermore, the selection of MgO type and characteristics seems crucial to achieve the desired properties for both MC and MS cements. We also point out research needed in this topic to pave the way for MgO-based cements to progress toward their promises.
Abstract licence: CC BY
Talyshinskii A, Pischetola A, Kamal W, et al.
2026
To define how reliable the benefits of potassium citrate (KCit) for stone prevention are framing this in terms of the number needed to treat (NNT). A targeted search of PubMed/MEDLINE, Embase, and the Cochrane Library was conducted through January 2025. For studies reporting recurrence rates in treatment and control groups, absolute risk reduction (ARR) and NNT were calculated. Two pivotal randomized trials in recurrent calcium stone formers demonstrated large ARRs with KCit or potassium-magnesium citrate, lowering 3-year recurrence rates from approximately 60%-80% in placebo groups to 10%-30% with therapy. Corresponding ARRs were around 50%, yielding NNTs of approximately 2 over 3 years. Evidence is strongest for calcium oxalate disease; data for calcium phosphate and brushite stones remain limited. In uric acid and cystine stones, alkalinization is first-line therapy, although precise NNT estimates are unavailable. KCit is one of the most effective preventive pharmacotherapies in nephrolithiasis. In recurrent calcium stone formers, treating two to three patients for approximately 3 years prevents one recurrence, representing a highly favorable benefit-risk profile when appropriately monitored and individualized by stone phenotype.
Abstract licence: CC BY-NC-ND
Y. Kitano, M. Okumura, M. Idogaki
Geochemical Journal, 1975
Y. Kitano
Bulletin of the Chemical Society of Japan, 1962
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.