Dantrolene 15mg/5ml oral suspension
Requires a prescription from a doctor or prescriber
Chemically, dantrolene is a hydantoin derivative, but does not exhibit antiepileptic activity like other hydantoin derivates such as phenytoin.
Official documents, adverse reaction reporting, and safety monitoring
Report a side effect
Submit a Yellow Card report to the MHRA
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.
View Drug Analysis Profile
Suspected adverse reactions reported for Dantrolene
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Interactive Drug Analysis Profiles for all medicines
Report a side effect
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.
View EudraVigilance report
Suspected adverse reactions reported for Dantrolene
About EudraVigilance
Learn about EU pharmacovigilance and safety monitoring
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
WHO defined daily dose (DDD)
100 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 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
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(1)
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
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
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: 8 · Randomised trials: 2 · 1972–2025
Showing the 50 most relevant studies, sorted by most relevant.
Brian Grunau, Matthew O. Wiens, Jeffrey R. Brubacher
Canadian Journal of Emergency Medicine, 2010
- Clinical Trials as Topic
- Dantrolene
- Fever
T. Krause, Mark Ulrich Gerbershagen, M. Fiege, et al.
Anaesthesia, 2004
- Dantrolene
- Malignant Hyperthermia
- Muscle Relaxants, Central
El-Harasis MA, Yoneda ZT, Varghese B, et al.
2025
C. Jung, A. Moretti, M. Mederos y Schnitzler, et al.
EMBO Molecular Medicine, 2012
- Polymorphic Catecholaminergic Ventricular Tachycardia
- Calcium
- Cells, Cultured
M. Büyükokuroğlu, I. Gülçin, M. Oktay, et al.
Pharmacological research, 2001
- Antioxidants
- Butylated Hydroxyanisole
- Butylated Hydroxytoluene
Fangyi Zhao, Pin Li, S. R. Wayne Chen, et al.
Journal of Biological Chemistry, 2001
- Adenine
- Central Nervous System Stimulants
- Arginine
Mary Elizabeth Kolb, M. L. Horne, Robert Martz
Anesthesiology, 1982
- Clinical Trials as Topic
- Dantrolene
- Injections, Intravenous
K.O. Ellis, John F. Carpenter
Naunyn-Schmiedeberg s Archives of Pharmacology, 1972
- Acetylcholine
- Aldehydes
- Aniline Compounds
Alan Ward, M. Chaffman, Eugene M. Sorkin
Drugs, 1986
- Calcium
- Central Nervous System
- Dantrolene
W. B. Van Winkle
Science, 1976
- Calcium
- Cats
- Dantrolene
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
1 found
Half-life
4 to 8 hours
Mechanism
Dantrolene depresses excitation-contraction coupling in skeletal muscle by bindi…
Food interactions
1 warning
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
70%
Half-life
4 to 8 hours
Protein binding
Metabolism
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 1085 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Dantrium may also undergo hydrolysis and subsequent oxidation forming nitrophenylfuroic acid.
Proteins and enzymes this drug interacts with in the body
PMID:11741831 PMID:16163667 PMID:18268335 PMID:18650434 PMID:26115329
Repeated very high-level exercise increases the open probability of the channel and leads to Ca(2+) leaking into the cytoplasm .
PMID:18268335
Can also mediate the release of Ca(2+) from intracellular stores in neurons, and may thereby promote prolonged Ca(2+) signaling in the brain. Required for normal embryonic development of muscle fibers and skeletal muscle. Required for normal heart morphogenesis, skin development and ossification during embryogenesis (By similarity)
Proteins that carry this drug through the body
ATC M03CA01
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)
Dantrolene
Additional database identifiers
Drugs Product Database (DPD)
2402
ChemSpider
5290202
BindingDB
50198767
Guide to Pharmacology
4172
ZINC
ZINC000002568036
HUGO Gene Nomenclature Committee (HGNC)
HGNC:10483
GenAtlas
RYR1
GeneCards
RYR1
GenBank Gene Database
J05200
GenBank Protein Database
337722
UniProt Accession
RYR1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:11583
GenAtlas
SERPINA7
GeneCards
SERPINA7
GenBank Gene Database
M14091
GenBank Protein Database
338697
UniProt Accession
THBG_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
ATC classifications (Wikidata)
Linked open data from Wikidata (Q421274), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.