Polysaccharide-iron complex 100mg/5ml oral solution sugar free
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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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1 branded products available
WHO defined daily dose (DDD)
110 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Tablets & capsules
(1)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. 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: 14 · Randomised trials: 4 · 1998–2026
Showing the 50 most relevant studies, sorted by most relevant.
Bhatt Y
2026
Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by cognitive decline, amyloid-β aggregation, tau pathology, oxidative stress, and neuroinflammation. Despite extensive research, effective disease-modifying therapies remain limited, underscoring the need for multi-target therapeutic strategies. Species of the genus Astragalus, widely used in traditional medicine, have gained attention for their neuroprotective potential due to diverse bioactive constituents, including saponins, flavonoids, and polysaccharides. This systematic review synthesizes current preclinical and emerging clinical evidence on the neuroprotective mechanisms of Astragalus species in AD. Literature was systematically analyzed in accordance with PRISMA guidelines. The findings indicate that Astragalus-derived compounds exert multi-target effects through modulation of key signaling pathways, including PI3K/Akt, Nrf2/ARE, MAPK, and NF-κB. These interactions collectively reduce oxidative stress, attenuate neuroinflammation, inhibit neuronal apoptosis, and improve synaptic function. Several studies further suggest roles in mitigating amyloid-β toxicity and tau hyperphosphorylation. Collectively, the evidence supports a systems-level pharmacological model in which Astragalus species mediate convergent neuroprotective effects across interconnected molecular pathways. However, translation to clinical application remains limited by insufficient human studies, variability in species-specific phytochemical profiles, and lack of standardized formulations. Future research should prioritize well-designed clinical trials, comparative species-level analyses, and mechanistic validation to establish the therapeutic potential of Astragalus in AD.
Abstract licence: CC BY-NC-ND
Ling Zhang, Zixing Zeng, Biyang Zhang, et al.
Frontiers in Public Health, 2025
- Pregnancy Complications, Hematologic
- Anemia, Iron-Deficiency
- Iron
Nurfarih Hanna, Mohd Zarif Fikri Bin Mohd, Muhammad Nabil Fikri Bin Mohd, et al.
Journal of Clinical and Nursing Research, 2026
Peng M, Kan X, Huang W
2026
Antibiotic resistance poses one of the most pressing threats to global public health, underscoring the urgent need for novel antimicrobial agents. Mushroom-derived polysaccharides have attracted considerable attention due to their structural diversity, low toxicity and various pharmacological activities. This review provides a comprehensive overview of the antiviral, antibacterial, and antifungal activities of polysaccharides isolated from edible and medicinal mushrooms against a range of pathogens, including multidrug-resistant species, with particular emphasis on the structural features that govern their efficacy. The mechanisms underlying these activities are examined, encompassing host immunomodulation, inhibition of pathogen attachment and entry, enzymatic inhibition of microbial replication and direct disruption of microbial cell integrity. Strategies to enhance antimicrobial potency are also discussed, covering chemical derivatization (e.g., sulfation, deacetylation), nanocomposite formulation and combination with conventional antimicrobials. Finally, the challenges of clinical translation including limited oral bioavailability, structural heterogeneity across preparations, and the lack of randomized clinical trial data in infectious disease indications, are critically evaluated. Addressing these gaps through standardization of production protocols, integrative structure-activity characterization and well-designed clinical trials will help advance the application of mushroom polysaccharides in medicine, food preservation, and agriculture.
Abstract licence: CC BY
Simon A. Levin
Ecosystems, 1998
Leo R. Zacharski, Deborah L. Ornstein, Steven Woloshin, et al.
American Heart Journal, 2000
Lu R, Zhang X, Cai X, et al.
2021
- Anemia, Iron-Deficiency
- Quality of Life
- Iron
R. Lu, Xu Zhang, Xu-Dong Cai, et al.
2021
John R. Charpie, Mary K. Dekeon, Caren S. Goldberg, et al.
The Journal of Thoracic and Cardiovascular Surgery, 2000
Shasha Dai, Zitong Hao, Yuchao Gao, et al.
Starch - Stärke, 2023
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.