Magnesium aspartate (magnesium 10mmol) granules for oral solution sachets
Requires a prescription from a doctor or prescriber
Magnesium aspartate is a magnesium salt of aspartic acid that is commonly used as a mineral supplement.
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MHRA alerts for Magnesium aspartate
Safety monitoring data
Yellow Card reports
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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 Magnesium aspartate
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3 branded products available
MHRA licensed products
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Mag-A (magnesium 10mmol) granules sachets
Ennogen Healthcare International 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.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(3)
Preventing recurrent hypomagnesaemia: oral magnesium glycerophosphate (ESUOM4)
Hypertension in pregnancy: diagnosis and management (NG133)
Eltrombopag for treating chronic immune thrombocytopenia (TA293)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
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Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
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: 27 · Randomised trials: 10 · 1984–2026
Showing the 50 most relevant studies, sorted by most relevant.
En-Bo Wu, Kuen-Lin Wu, Wei-Ti Hsu, et al.
Pharmaceuticals, 2025
Habiblah Jagunmolu, Emmanuel Oyetola, Yusuff Lawal, et al.
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2026
Zhou J, Wen Y, Xu S, et al.
2026
- Receptors, N-Methyl-D-Aspartate
- Excitatory Amino Acid Antagonists
- Acute Pain
Owayed A, Alshammari HA, Aljumaiaan M, et al.
2025
Tarimah K, Fu’adi I, Wiyarta E, et al.
2026
Leyva-Velázquez AP, Reyes-Avitia V, Simental-Mendía LE
2026
Mohammadi S, Palermo A, Ojani P, et al.
2026
- Magnesium
- Dietary Supplements
- Cardiometabolic Risk Factors
Background: Evidence regarding the impacts of magnesium (Mg) supplementation on cardiometabolic risk factors (CMRFs) remains inconsistent. Objectives: This systematic review and dose-response meta-analysis evaluated effects of Mg supplementation on anthropometric indices, liver and kidney function, lipid and glycemic profiles, blood pressure, and inflammatory biomarkers. Methods: A systematic search of electronic databases up to May 2026 identified 78 eligible randomized controlled trials. Results: Mg supplementation significantly reduced body weight (weighted mean difference [WMD]: -0.70 kg; 95% confidence interval [CI]: -1.30, -0.09), diastolic blood pressure (WMD: -1.58 mmHg; 95% CI: -2.50, -0.65), homeostasis model assessment of insulin resistance (WMD: -0.48; 95% CI: -0.79, -0.18), low-density lipoprotein cholesterol (WMD: -3.21 mg/dL; 95% CI: -5.27, -1.15), fasting blood glucose (WMD: -3.60 mg/dL; 95% CI: -6.13, -1.06), systolic blood pressure (WMD: -2.50 mmHg; 95% CI: -4.08, -0.91), glycated hemoglobin (WMD: -0.15%; 95% CI: -0.26, -0.03), triglycerides (WMD: -9.24 mg/dL; 95% CI: -16.87, -1.61), and interleukin-6 levels (WMD: -1.10 pg/mL; 95% CI: -1.93, -0.27) compared with controls. High-density lipoprotein cholesterol concentrations significantly increased (WMD: 1.45 mg/dL; 95% CI: 0.37, 2.54). No significant effects were identified on hip circumference, alanine aminotransferase, waist circumference, tumor necrosis factor-α, creatinine, C-reactive protein, body mass index, total cholesterol, fasting insulin, body fat percentage, and aspartate aminotransferase. Most RCTs (79.5%) administered Mg doses ≥ 300 mg/day, and 66.7% had intervention durations ≥ 12 weeks; however, evidence from higher-dose (≥500 mg/day) and longer-term (≥25 weeks) interventions remained limited. Conclusions: Mg supplementation was associated with significant improvements in several CMRFs, including body weight, lipid and glycemic profiles, blood pressure, and interleukin-6 levels. However, these effects were generally modest, and their clinical relevance remains uncertain given the variable certainty of evidence across outcomes.
Abstract licence: CC BY
Hyun-Jung Shin, H. Na, S. Do
Nutrients, 2020
H. You, Seo-Eun Cho, Seung-Gul Kang, et al.
Nordic Journal of Psychiatry, 2018
Fateme Bayat, Seideh Hanieh Alamolhoda, Hadis Shahrahmani, et al.
Majallah-i Zanān, Māmā̓ī va Nāzā̓ī-i Īrān, 2021
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
Investigational
Major interactions
70 found
Half-life
Not available
Mechanism
Not available
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 251 interactions
ATC A12CC05
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)
Magnesium aspartate
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72