Selenium 100micrograms/2ml oral solution unit dose ampoules
Requires a prescription from a doctor or prescriber
Selenium is a trace metal in the human body particularly important as a component of glutathione peroxidase, an important enzyme in the prevention of cellular damage by free radicals and reactive oxygen species [FDA Label]
Safety information for pregnancy and breastfeeding
Pregnancy
Always consult your doctor or midwife before taking any medicine during pregnancy or while breastfeeding. Source: DrugBank (CC BY-NC 4.0).
Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
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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Suspected adverse reactions reported for Selenium
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Submit a Yellow Card report to the MHRA
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
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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Suspected adverse reactions reported for Selenium
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
1 branded products available
Part of the Selsun brand family (generic: Selenium)
MHRA licensed products
View all licensed products for Selenium on the MHRA register
Selenase 100micrograms/2ml oral solution 2ml unit dose ampoules
This is the NHS Drug Tariff indicative price used for reimbursement purposes. It may not reflect the price paid by patients or pharmacies.
View full Drug TariffSource: NHS Drug Tariff via NHSBSA. Derived from dm+d VMPP (Virtual Medicinal Product Pack) pricing data. 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
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(4)
SeHCAT (tauroselcholic [75 selenium] acid) for diagnosing bile acid diarrhoea (HTG598)
Thyroid disease: assessment and management (NG145)
Nutrition support for adults: oral nutrition support, enteral tube feeding and parenteral nutrition (CG32)
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. 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: 47 · Randomised trials: 3 · 1996–2026
Showing the 50 most relevant studies, sorted by most relevant.
M. Vinceti, T. Filippini, K. Rothman
European Journal of Epidemiology, 2018
Xianlei Cai, Chen Wang, Wanqi Yu, et al.
Scientific Reports, 2016
J. Wichman, K. Winther, S. Bonnema, et al.
Thyroid, 2016
Gemma Flores‐Mateo, Ana Navas‐Acién, Roberto Pastor‐Barriuso, et al.
American Journal of Clinical Nutrition, 2006
- Dietary Supplements
- Coronary Disease
- Predictive Value of Tests
O. Tamtaji, Reza Heidari-soureshjani, N. Mirhosseini, et al.
Clinical nutrition, 2019
Xi Zhang, Conglin Liu, Jianjun Guo, et al.
European Journal of Clinical Nutrition, 2016
D. Jenkins, D. Kitts, E. Giovannucci, et al.
The American Journal of Clinical Nutrition, 2020
G. Genchi, G. Lauria, Alessia Catalano, et al.
International Journal of Molecular Sciences, 2023
Fan Zhang, Xue‐Lian Li, Yumiao Wei
Biomolecules, 2023
- Diabetes Mellitus, Type 2
- Selenium
- Trace Elements
M. Rayman, K. Winther, R. Pastor-Barriuso, et al.
Free Radical Biology and Medicine, 2018
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
None known
Half-life
1.7 days
Mechanism
Selenium is first metabolized to selenophosphate and selenocysteine.
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
90%
[A19385]
Tmax of 9.17h.
Half-life
1.7 days
[A19385]…
Metabolism
Elimination
[A19383]…
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 720 interactions
Serum selenium correlates weakly with symtoms. Blood chemistry as well as liver and kidney function are normally unnaffected. Acute toxicity presents as stupor, respiratory depression, and hypotension.
ST elevations and t-wave changes characteristic of myocardial infarction may be observed.
The most important selenoproteins seem to be the glutathione peroxidases and thioredoxin reductases which are part of the body's defenses againts reactive oxygen species (ROS) [A19375]. The importance of selenium in these anti-oxidant proteins has been implicated in the reduction of atherosclerosis by preventing the oxidation of low density lipoprotein [A19384] [A19380]. Selenium supplementation is also being investigated in the prevention of cancer and has been suggested to be beneficial to immune function [A19384] [A19381] [A19382].
How the body processes this drug — absorption, distribution, metabolism, and elimination
[A19385]
Tmax of 9.17h.
[A19385]
For day 1-2 half life was 1.7 days. For day 2-3 half life was 3 days. For day 3-14 half life was 11.1 days.
[A19375]
Selenide is further metabolized to selenocystein by cysteine synthases and to selenophosphate by selenophosphate synthases. Selenide is also metabolized progressively to methyl-selenol, dimethyl selenide, then trimethylselenonium. Selenocysteine is degraded to methyl-selenol, pyruvate and ammonia by cysteine beta lyase.
Selenocystein reacts with oxygen to form selenocysteine selenoxide which spontaneously degrades to methylselenic acid, pyruvate and ammonia. Methylselenic acid can be converted to methylselenol via conjugation with thiol groups on proteins like glutathione.
[A19383]
The amount excreted as 1beta-methylseleno-N-acetyl-d-galactosamine plateaus at doses around 2microg after which the amount excreted as trimethylselenonium increases. Some selenium is also excreted in feces when given orally .
[A19385]
Enzymes involved in drug metabolism — important for understanding drug interactions
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)
Selenium
Additional database identifiers
Drugs Product Database (DPD)
2295
Drugs Product Database (DPD)
6319
Drugs Product Database (DPD)
704
ChemSpider
4885617
HUGO Gene Nomenclature Committee (HGNC)
HGNC:18161
GeneCards
SCLY
UniProt Accession
SCLY_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:4623
GenAtlas
GSR
GeneCards
GSR
GenBank Gene Database
X15722
GenBank Protein Database
31825
UniProt Accession
GSHR_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:12437
GenAtlas
TXNRD1
GeneCards
TXNRD1
GenBank Gene Database
X91247
GenBank Protein Database
1237038
UniProt Accession
TRXR1_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
Molecular structure

Linked open data from Wikidata (Q876), 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.