Liquid paraffin / Magnesium hydroxide oral emulsion sugar free
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Liquid paraffin / Magnesium hydroxide oral emulsion sugar free
Alliance Healthcare (Distribution) Ltd
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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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: 8 · Randomised trials: 2 · 2001–2026
Showing the 50 most relevant studies, sorted by most relevant.
Calvin C. Willhite, Nataliya A. Karyakina, Robert A. Yokel, et al.
Critical Reviews in Toxicology, 2014
- Aluminum
- Aluminum Hydroxide
- Aluminum Oxide
Amer SA, Abo-Elnour DE, Abbas A, et al.
2025
- Hypertension
- Calcium
- Magnesium
BackgroundHypertension, the first global modifiable risk factor for cardiovascular disease (CVD) morbidity and mortality, is a consequential and remediable threat to the health of individuals and society. Therefore, we conducted this study to explore the role of calcium (Ca++), magnesium (Mg++), and vitamin D (Vit-D) supplementation as complementary therapies for hypertension, focusing on their effects on systolic blood pressure (SBP), diastolic blood pressure (DBP), and pulse rate.MethodsThis systematic review and meta-analysis examined relevant 6509 articles in PubMed, Scopus, Web of Science, and Cochrane CENTRAL up to October 2024. The primary outcome was the difference in blood pressure measurements (systolic and diastolic) and the pulse rate. The extracted data were analyzed using Open Meta Analyst software.ResultsThis systematic review and meta-analysis included 40 studies; of them, 24 studies were analyzed. Ca++ was associated with a significant drop in the DBP (MD: -2.04, 95% CI [-3.39, -0.69], P = 0.01), but not in the SBP (P = 0.34) or pulse rate (P = 0.84). Mg++ significantly reduced DBP (MD: -1.64, 95% CI [-3.19, -0.09], P = 0.04), but had no significant effect on the SBP (P = 0.16) or pulse rate (P = 0.81). The estimated effect of Vit-D showed a significant reduction in SBP (MD: -2.83, 95% CI [-5.47, -0.199], P = 0.04) and DBP (MD: -1.64, 95% CI [-2.97, -0.3], P = 0.01).ConclusionCa++ and Mg++ significantly reduced DBP but had no significant effect on SBP or the pulse rate. Whereas, vitamin D significantly reduced SBP and DBP.
Abstract licence: CC BY
Li S, Xu H, Geng T, et al.
2026
C. Y. Tai, C. Tai, Ming-Hui Chang, et al.
Industrial & Engineering Chemistry Research, 2007
Liye Xia, Siyu Zhang, Zhiguang Guo
Advanced Materials Interfaces, 2023
Junsi Luo, Yiteng Cui, Laijun Xu, et al.
Journal of Nanobiotechnology, 2025
- Hydroxides
- Tissue Engineering
- Regenerative Medicine
G. Song, Sude Ma, G. Tang, et al.
Energy, 2010
Vladimir Chubanov, Silvia Ferioli, Annika Wisnowsky, et al.
eLife, 2016
- Embryonic Development
- Intestinal Mucosa
- Magnesium
Nasim Golafshan, Elke Vorndran, Stefan Zaharievski, et al.
Biomaterials, 2020
- Magnesium Compounds
- Tissue Scaffolds
- Bone Regeneration
Vincent Coger, Nina Million, Christoph Rehbock, et al.
Biological Trace Element Research, 2018
- Wound Healing
- Copper
- Disease Models, Animal
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.