Calcium gluconate 544mg/5ml / Calcium lactate 276mg/5ml oral solution
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MHRA alerts for Calcium gluconate + Calcium lactate
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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
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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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: 7 · Randomised trials: 2 · 1980–2026
Showing the 50 most relevant studies, sorted by most relevant.
Silva C, Marcos P
2025
IntroductionIntravenous (IV) fluid therapy plays a vital role in modern medical practice, particularly in critical care management. This review aims to summarize the composition, indications, and contraindications of IV fluids, serving as a useful resource for healthcare professionals.MethodsReview of the literature published in MEDLINE using PubMed and Web of Science, between 2009 and 2024. Systematic reviews, meta-analyses, expert reviews, and guidelines were preferred for analysis.ResultsIV fluids can be administered for various reasons, including resuscitation, correction of electrolyte imbalances, or more critical cases. They can be divided into 2 categories: crystalloids and colloids. Crystalloids, in turn, can be subdivided into unbalanced solutions, such as salines (0.45%, 0.9%, 3%, and 20%) and dextrose 5%, or balanced solutions, such as Ringer lactate and polyelectrolytic solutions. Colloids can be derived from plasma, such as 5% albumin, or semisynthetic, such as 4% modified fluid gelatin. Crystalloids are generally more cost-effective, have a lower risk of allergic reactions, and are more readily available than colloids. However, the use of each solution should be individualized based on the patient's specific needs and corresponding conditions.ConclusionsIt is essential to have a thorough understanding of available IV fluid solutions to select the best option for each patient's condition at any given time. This review summarizes the most relevant information to guide these decisions. Future research should develop IV fluids that combine the benefits of colloids and crystalloids for safer, more personalized, and cost-effective treatments.
Abstract licence: CC BY-NC-ND
Deborah A. Straub
Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition, 2007
C Kanaris, A Janjanam, S Palaniappan
Association of paediatric emergency medicine, 2020
K. Arasu, Chung Yuan Chang, Soon Yee Wong, et al.
Osteoporosis International, 2023
Li P, Li M, Yin W, et al.
2025
- Calcium
- Citric Acid
- Anticoagulants
Emanuel Manzurola, Alexander Apelblat
The Journal of Chemical Thermodynamics, 2002
Wenqiang Liu, Nathanael W L Low, B. Feng, et al.
Environmental science & technology, 2010
M. S. Sheikh, C. S. Santa Ana, M. Nicar, et al.
The New England journal of medicine, 1987
Cetani F, Bertoldo F, Bononi M, et al.
2026
- Hypoparathyroidism
- Calcium
- Parathyroid Hormone
BackgroundHypoparathyroidism (HypoPT) is a rare endocrine disorder characterized by insufficient or absent secretion of parathyroid hormone (PTH), which results in hypocalcemia, hyperphosphatemia, and disruption of calcium phosphate homeostasis. Despite advances in understanding its pathophysiology and management, HypoPT remains a complex and impactful condition associated with significant morbidity, impaired quality of life, and long-term complications affecting the skeletal, renal, and neurological systems.MethodsA literature search was performed on PubMed. Articles were selected based on their relevance to the main topic of the review, with particular attention to recent studies.ResultsThis review provides a comprehensive synthesis of the current knowledge on HypoPT, addressing its epidemiology, underlying pathophysiological mechanisms, genetic and acquired etiologies, clinical manifestations, diagnostic strategies, and chronic disease-related complications. Emphasis is placed on the genetic spectrum of the disease, challenges of postsurgical management, and burden of conventional therapy, which often fails to fully restore mineral homeostasis and patient well-being. The evolving therapeutic landscape is detailed, highlighting advances from traditional calcium and active vitamin D supplementation to innovative PTH replacement strategies. Among these, palopegteriparatide and eneboparatide (phase 3 clinical trial ongoing) are reshaping treatment paradigms by enabling more physiological restoration of calcium-phosphate balance, reducing complications, and improving patient-centered outcomes, including renal function and quality of life.ConclusionsBy integrating clinical expertise with the latest research developments, this review offers an updated and holistic perspective on HypoPT management, aiming to support clinicians in delivering effective and individualized care to patients across the spectrum of disease severity.
Abstract licence: CC BY-NC-ND
Miller A, Omassoli J, Simpson J, et al.
2026
Calcium plays an essential role in myocardial contractility, excitation-contraction coupling, and vascular tone. In cardiothoracic surgery, calcium supplementation is frequently administered during weaning from cardiopulmonary bypass (CPB) and in the early postoperative period to support haemodynamics. Despite its widespread use, the evidence base underpinning this practice remains limited and inconsistent. This narrative review explores the physiological rationale for calcium supplementation in the cardiothoracic surgical population, synthesises existing experimental and clinical data, and considers potential benefits and risks relevant to contemporary intensive care practice. Animal models suggest that calcium desensitisation contributes to myocardial dysfunction following hypothermic circulatory arrest, with supplementation theoretically improving contractility. In human studies, calcium administration during CPB weaning or in the immediate post-CPB period has been associated with transient increases in mean arterial pressure, systemic vascular resistance and left ventricular stroke work index. However, these effects are short-lived and data beyond the early postoperative phase remains limited. Potential risks of calcium supplementation include exacerbation of ischaemia-reperfusion injury, arrhythmogenesis, graft vasospasm, and tissue injury related to extravasation. The absence of specific guideline recommendations, in contrast to established consensus for vasopressor therapy, likely contributes to international variability in practice. Most studies are small, dated, or proof-of-concept and no high-quality randomised controlled trials have examined patient-centred outcomes such as vasopressor duration, organ dysfunction, or length of stay. Further multicentre observational and target-trial emulation studies are warranted to clarify the role of ionised calcium use in contemporary perioperative and intensive care practice.
Abstract licence: CC BY
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.