Sodium valproate 300mg suppositories
Requires a prescription from a doctor or prescriber
Antiepileptic drug
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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.
EudraVigilance
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1 branded products available
Part of the Epilim brand family (generic: Sodium valproate)
MHRA licensed products
View all licensed products for Sodium valproate on the MHRA register
WHO defined daily dose (DDD)
1.5 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
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(11)
Epilepsies in children, young people and adults (NG217)
Bipolar disorder: assessment and management (CG185)
Antenatal and postnatal mental health (QS115)
Antenatal and postnatal mental health: clinical management and service guidance (CG192)
Fenfluramine for treating seizures associated with Dravet syndrome (TA808)
Transcutaneous stimulation of the cervical branch of the vagus nerve for cluster headache and migraine (HTG408)
Cenobamate for treating focal onset seizures in epilepsy (TA753)
Medicines associated with dependence or withdrawal symptoms: safe prescribing and withdrawal management for adults (NG215)
Cannabidiol with clobazam for treating seizures associated with Lennox–Gastaut syndrome (TA615)
Cannabidiol with clobazam for treating seizures associated with Dravet syndrome (TA614)
Suspected neurological conditions: recognition and referral (NG127)
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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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
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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: 14 · Randomised trials: 16 · 1977–2026
Showing the 50 most relevant studies, sorted by most relevant.
M de Silva, B M Macardle, M McGowan, et al.
The Lancet, 1996
- Anticonvulsants
- Carbamazepine
- Epilepsy
Andrew Heller, Paul Chesterman, Robert Elwes, et al.
Journal of Neurology Neurosurgery & Psychiatry, 1995
- Epilepsies, Partial
- Epilepsy, Generalized
- Epilepsy, Tonic-Clonic
Tan S, Ng JS, Tang C, et al.
2024
- Valproic Acid
- Anticonvulsants
- Palliative Care
Askar G, Askar O, Altuhafy M, et al.
2024
Hargreaves F, Crewe J, Daniel S
2025
Dipender Gill, Sheena Derry, Philip J Wiffen, et al.
Cochrane Database of Systematic Reviews, 2011
- Analgesics
- Diabetic Neuropathies
- Fibromyalgia
Detria Rahma Gasti, Aulia Sita Hapsari, Karima Iffani Ulifah
Pediatric Sciences Journal, 2023
Yifei Zhu, Junlan Yang, Xinjian Zhu
Seizure, 2021
S. Nevitt, A. Marson, Jennifer Weston, et al.
The Cochrane database of systematic reviews, 2018
Zhen-Ye Ji, Yi-Qian Huang, Wen-Zhen He
Frontiers in Neurology, 2022
Background: Among antiepileptic drugs (AEDs), sodium valproate alone or in the combination of topiramate (TPM) for treating refractory epilepsy was controversial. This meta-analysis aimed to systematically evaluate the clinical effects of these two regimens in this population.Methods: Relevant studies up to August 2021 were identified through systematic searches of CNKI, Wanfang, PubMed, and Embase databases. We assessed the effectiveness and the frequency of absence seizures, atonic seizures, and tonic–clonic seizures. The included literature's risk of bias was evaluated using the Cochrane Collaboration's Risk of Bias tool. Sensitivity analysis was conducted to confirm the results' stability. STATA 15.0 was utilized for all pooled analyses in the included studies.Results: Totally 10 articles were determined for our meta-analysis, involving 976 patients with epilepsy in total (combined group, n = 488; monotherapy group, n = 488). The results of this meta-analysis indicated that the total effective rate of sodium valproate combined with TPM was higher than that of sodium valproate alone (random-effect model: OR = 3.52; 95% CI 1.47 to 8.47; p < 0.001; I2 = 73.8%). The frequency of absence seizures in the combined group was lower (fixed-effect model: WMD = −6.02; 95% CI −6.50 to −5.54; I2 = 0.0%) than that in the monotherapy group, with a statistical difference (p < 0.05). The combined group had lower frequency of atonic seizures (WMD = −4.56, 95% CI −6.02 to −3.10; I2 = 82.6%) and lower frequency of tonic–clonic seizures (WMD = −3.32; 95% CI −4.75 to −1.89; I2 = 96.4%). In addition, the distinct difference of adverse events was non-existent between two groups.Conclusions: Sodium valproate combined with TPM was more effective than sodium valproate alone for epilepsy therapy. This meta-analysis provides feasibility data for a larger-scale study on AED therapy of refractory epilepsy and may contribute to better therapy strategies for epilepsy clinically.
Abstract licence: CC BY 4.0
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.
Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q240642), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.