Sodium dihydrogen phosphate dihydrate 780mg/5ml oral suspension
Requires a prescription from a doctor or prescriber
Sodium phosphate is a saline laxative that is thought to work by increasing fluid in the small intestine.
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Drug safety updates
MHRA alerts for Sodium dihydrogen phosphate dihydrate
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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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.
EudraVigilance
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1 branded products available
WHO defined daily dose (DDD)
50 gram
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 BNF/ATC mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
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
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
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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: 2 · Trials: 1 · 1946–2026
Showing the 50 most relevant studies, sorted by most relevant.
Frits Zernike
Journal of the Optical Society of America, 1964
R. Parsons, F. Zobel
Journal of Electroanalytical Chemistry, 1965
J. Jerphagnon, S. K. Kurtz
Physical Review B, 1970
W. P. Mason
Physical Review, 1946
Tien S, Kayser V
2025
Therapeutic proteins such as insulin and monoclonal antibodies (mAbs) have become an essential part of the modern healthcare system and play a crucial role in the treatment of various diseases including cancer and autoimmune disorders. However, their long-term stability is a significant concern, affecting efficacy, shelf-life, and safety. Ionic liquids (ILs) have emerged as promising additives to enhance protein stability and address the aforementioned issues. Indeed, recent studies indicate that biocompatible ILs, particularly choline-based ILs, have significant potential to improve stability while preserving proteins' functionality. For instance, choline valinate has been shown to increase the melting temperature of insulin by almost 13 °C (Judy and Kishore Biochimie 207:20-32, 2023), while choline dihydrogen phosphate has increased the melting temperature of trastuzumab by over 21 °C (Reslan et al. Chem Commun 54:10622-10625, 2018). However, it is worth noting that the use of some ILs introduces a complex trade-off: while they can increase thermal stability, they may also promote protein unfolding, thereby reducing conformational stability. Moreover, selecting the most suitable IL and its optimal concentration is challenging, as different protein formulations may exhibit varying effects. This review provides a comprehensive overview of the existing literature on ILs as stabilisers for insulin and mAbs, documenting specific IL-protein combinations and conditions to identify potential future stabilising agents for biologics in general.
Abstract licence: CC BY
Mohammed Taghi Zafarani-Moattar, Rahmat Sadeghi
Fluid Phase Equilibria, 2001
Mohammed Taghi Zafarani-Moattar, Rahmat Sadeghi
Fluid Phase Equilibria, 2002
E. F. Burguera, H. Xu, M. Weir
Journal of biomedical materials research. Part B, Applied biomaterials, 2006
Milad Hammal, Daniel Černý, Iva Voborná, et al.
Stomatológ, 2020
V. Joshi, M. Joshi
Crystal Research and Technology, 2003
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
Approved
Major interactions
44 found
Half-life
Not available
Mechanism
Sodium phosphate is thought to work by increasing the amount of solute present i…
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
1-3h
[A19448]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 781 interactions
[L799]
Phosphate toxicity is likely due to the disturbance of other electrolytes when phosphate levels are high, producing symptoms including tetany, dehydration, hypotension, tachycardia, hyperpyrexia, cardiac arrest and coma .
[A19449]
Risk of raising phosphate levels through use of sodium phosphate appears to be higher in smaller patients .
[A19448]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[A19448]
Proteins that transport this drug across cell membranes
PMID:11009570 PMID:16790504 PMID:17494632 PMID:19726692 PMID:7929240 PMID:8041748
May play a role in extracellular matrix and cartilage calcification as well as in vascular calcification .
PMID:11009570
Essential for cell proliferation but this function is independent of its phosphate transporter activity PMID:19726692
PMID:12205090 PMID:15955065 PMID:16790504 PMID:17494632 PMID:22327515 PMID:28722801 PMID:30704756
Plays a critical role in the determination of bone quality and strength by providing phosphate for bone mineralization (By similarity). Required to maintain normal cerebrospinal fluid phosphate levels (By similarity). Mediates phosphate-induced calcification of vascular smooth muscle cells (VCMCs) and can functionally compensate for loss of SLC20A1 in VCMCs (By similarity)
PMID:12324554 PMID:20335586 PMID:26047794 PMID:8327470
The cotransport has a Na(+):Pi stoichiometry of 3:1 and is electrogenic (By similarity)
PMID:11880379
The cotransport has a Na(+):Pi stoichiometry of 2:1 and is electroneutral (By similarity)
ATC A06AG01
ATC V03AG05
ATC A06AD17
ATC B05XA09
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)
Sodium phosphate, monobasic
Matched from: Sodium dihydrogen phosphate dihydrate
Additional database identifiers
Drugs Product Database (DPD)
293
Drugs Product Database (DPD)
4753
Drugs Product Database (DPD)
4759
Drugs Product Database (DPD)
20445
ChemSpider
22626
HUGO Gene Nomenclature Committee (HGNC)
HGNC:10946
GeneCards
SLC20A1
UniProt Accession
S20A1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:10947
GeneCards
SLC20A2
UniProt Accession
S20A2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:11019
GeneCards
SLC34A1
UniProt Accession
NPT2A_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:11020
GeneCards
SLC34A2
Guide to Pharmacology
1136
UniProt Accession
NPT2B_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:20305
GeneCards
SLC34A3
UniProt Accession
NPT2C_HUMAN
DrugBank citations
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Structured knowledge from the free knowledge base
Molecular structure
ATC classifications (Wikidata)
Linked open data from Wikidata (Q409501), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. Molecular structure images from Wikimedia Commons.