Lithium citrate 509mg/5ml oral solution
Requires a prescription from a doctor or prescriber
Pharmaceutical preparation of the element lithium, used primarily as a psychiatric medication for mood disorders
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Suspected adverse reactions reported for Lithium citrate
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8 branded products available
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Li-Liquid 509mg/5ml oral solution
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.
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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: 7 · Randomised trials: 1 · 1996–2026
Showing the 50 most relevant studies, sorted by most relevant.
Sabtiari TN, Myrtle S, Orfanos S, et al.
2025
- Lithium
- Lithium Compounds
- Cognition
BackgroundLithium, a mainstay treatment for bipolar disorders, has shown promise in treating cognitive impairments. However, concerns about cognition-related side effects persist.AimsWe aimed to synthesise the evidence on how lithium affects cognition by comparing cognitive performance before and after starting lithium treatment.MethodsA systematic search was conducted to identify studies examining lithium's effects on cognition. The review considered studies with adult human participants that reported quantitative cognitive outcomes using within-subject comparisons between lithium-absent and lithium-present conditions.ResultsThirty-two articles describing 30 studies were included (727 participants, approximately 54% female, mean age ± 50 years old). The studies exhibited significant heterogeneity within cognitive domains, including global cognition (15 studies), memory (19 studies), processing and psychomotor speed (8 studies), attention (9 studies), verbal fluency (4 studies) and executive function (6 studies). The included studies comprised 16 randomised controlled trials (RCTs) and 14 non-RCTs, with study populations ranging from individuals with affective disorders (13 studies) to neurocognitive disorders (11 studies) and healthy individuals (6 studies). Some studies reported cognitive enhancements, particularly in individuals with affective disorders, while others documented declines or mixed results.ConclusionsDefinitive conclusions regarding lithium's isolated cognitive effects remain elusive, particularly considering the influence of factors such as affective state, population and methodological heterogeneity among studies. Further research is needed to conclusively determine the raw cognitive impacts of lithium therapy, requiring larger RCTs across distinct populations. Prioritising the resolution of main symptoms should remain the primary therapeutic goal of lithium treatment.
Abstract licence: CC BY
Hovgesen SV, Licht RWW, Straszek SPV, et al.
2025
- Lithium Compounds
- Piperazines
- Antidepressive Agents
Guoxin Gao, H. Wu, X. Lou
Advanced Energy Materials, 2014
E. Y. Villegas-Vázquez, L. Quintas-Granados, H. Cortés, et al.
Life, 2023
Min Yu, Zehui Zhang, Feng Xue, et al.
Separation and Purification Technology, 2019
Islam M, Ahmed MS, Faizan M, et al.
2024
The rapid design of advanced materials depends on synthesis parameters and design. A wide range of materials can be synthesized using precursor reactions based on chelated gel and organic polymeric gel pathways. The desire to develop high-performance lithium-ion rechargeable batteries has motivated decades of research on the synthesis of battery active material particles with precise control of composition, phase-purity, and morphology. Among the most common methods reported in the literature to prepare precursors for lithium-ion battery active materials, sol-gel is characterized by simplicity, homogeneous mixing, and tuning of the particle shape. The chelate gel and organic polymeric gel precursor-based sol-gel method is efficient to promote desirable reaction conditions. Both precursor routes are commonly used to synthesize lithium-ion battery cathode active materials from raw materials such as inorganic salts in aqueous solutions or organic solvents. The purpose of this review is to discuss synthesis procedure and summarize the progress that has been made in producing crystalline particles of tunable and complex morphologies by sol-gel synthesis that can be used as active materials for lithium-ion batteries.
Abstract licence: CC BY
Sager M
2025
This review contains a compilation of data about the occurrence, mining, refining, and biological actions of lithium, without claiming completeness of knowledge. This should give a baseline for judging future pollutions of environmental and agricultural items and human nutrition and may show still existing gaps of screening. Emerging electromobility and use of computers leads to a steep increase in Li-based batteries, which are a source of hazardous waste unless recycled. Lack of recovery methods from effluents and sewage, however, will increase pollution with soluble Li-salts from increasing mining and waste in the future; therefore, biochemical effects of levels out of ambient range have been included. Many published data are hidden in multi-element tables, including the data of the author. Mobile fractions of soils and soil-to-plant transfer, as well as retainment in animal tissues, are low. A lot of data, starting from geology via soils, plants, water, and human nutrition, lead to a largely unknown average daily intake for men. With respect to nutrition of dairy cows, the contribution of Li from water was highest among all elements investigated, but only 4% of intake. Main sources for human nutrition are mineral water and table salt. Li is not labelled on mineral water bottles, nor table salt, which are the main sources. Though some data have been gathered, for human nutrition, the average daily intake is uncertain to estimate because some mineral waters are quite high in Li.
Abstract licence: CC BY
Raveendran Priyadarsini, N. Venkateswaramurthy
Journal of Drug Delivery and Therapeutics, 2023
Xie S, Pang X, Yu Z, et al.
2025
BackgroundLithium carbonate has a narrow therapeutic index, and postoperative anatomical/physiological changes after bariatric surgery may markedly alter its pharmacokinetics.CaseA 25-year-old woman with bipolar disorder on long-term lithium therapy developed altered consciousness and profound sinus bradycardia (nadir 27 bpm) approximately 7 weeks after single-incision laparoscopic sleeve gastrectomy. Laboratory testing revealed hyponatremia, acute kidney injury, and a serum lithium level of 4.16 mmol/L.Interventions and outcomesLithium and other psychotropics were discontinued, fluid resuscitation and inotropic support were initiated, and three consecutive sessions of continuous renal replacement therapy (CRRT) were performed. Serum lithium normalized without rebound, Sinus bradycardia recovered, and the patient was discharged without pacemaker implantation. During follow-up, lithium was permanently discontinued and replaced with lamotrigine. Mood remained stable without cardiac or neurologic sequelae.ConclusionPost-bariatric patients receiving lithium should be considered high risk for intoxication. Routine monitoring with early recognition and multidisciplinary collaboration is essential to prevent complications. This case further shows that even extreme lithium-induced bradycardia can be fully reversible with timely withdrawal and extracorporeal clearance, highlighting the need to address reversible causes before permanent pacing.
Abstract licence: CC BY
A. B. Rech, A. Kinoshita, P. Donate, et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 2022
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
139 found
Half-life
Not available
Mechanism
The precise mechanism of action of Li+ as a mood-stabilizing agent is currently unknown.
Food interactions
5 warnings
Human targets
4 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 1079 interactions
Proteins and enzymes this drug interacts with in the body
PMID:17068342
It is likely that IMPA2 has an as yet unidentified in vivo substrate(s) .
PMID:17068342
Has been implicated as the pharmacological target for lithium (Li(+)) action in brain PMID:17068342
PMID:17068342 PMID:8718889 PMID:9462881
Is also able to dephosphorylate scyllo-inositol-phosphate, myo-inositol 1,4-diphosphate, scyllo-inositol-1,3-diphosphate and scyllo-inositol-1,4-diphosphate .
PMID:17068342
Also dephosphorylates in vitro other sugar-phosphates including D-galactose-1-phosphate, glucose-1-phosphate, glucose-6-phosphate, fructose-1-phosphate, beta-glycerophosphate and 2'-AMP .
PMID:17068342 PMID:8718889 PMID:9462881
Responsible for the provision of inositol required for synthesis of phosphatidylinositols and polyphosphoinositides, and involved in maintaining normal brain function .
PMID:26416544 PMID:8718889
Has been implicated as the pharmacological target for lithium (Li(+)) action in brain, which is used to treat bipolar affective disorder .
PMID:17068342
Is equally active with 1D-myo-inositol 1-phosphate, 1D-myo-inositol 3-phosphate and D-galactose 1-phosphate PMID:9462881
PMID:11430833 PMID:12554650 PMID:14690523 PMID:16484495 PMID:1846781 PMID:20937854 PMID:9072970
Requires primed phosphorylation of the majority of its substrates .
PMID:11430833 PMID:16484495
In skeletal muscle, contributes to insulin regulation of glycogen synthesis by phosphorylating and inhibiting GYS1 activity and hence glycogen synthesis .
PMID:8397507
May also mediate the development of insulin resistance by regulating activation of transcription factors .
PMID:8397507
Regulates protein synthesis by controlling the activity of initiation factor 2B (EIF2BE/EIF2B5) in the same manner as glycogen synthase .
PMID:8397507
In Wnt signaling, GSK3B forms a multimeric complex with APC, AXIN1 and CTNNB1/beta-catenin and phosphorylates the N-terminus of CTNNB1 leading to its degradation mediated by ubiquitin/proteasomes .
PMID:12554650
Phosphorylates JUN at sites proximal to its DNA-binding domain, thereby reducing its affinity for DNA .
PMID:1846781
Phosphorylates NFATC1/NFATC on conserved serine residues promoting NFATC1/NFATC nuclear export, shutting off NFATC1/NFATC gene regulation, and thereby opposing the action of calcineurin .
PMID:9072970
Phosphorylates MAPT/TAU on 'Thr-548', decreasing significantly MAPT/TAU ability to bind and stabilize microtubules .
PMID:14690523
MAPT/TAU is the principal component of neurofibrillary tangles in Alzheimer disease .
PMID:14690523
Plays an important role in ERBB2-dependent stabilization of microtubules at the cell cortex .
PMID:20937854
Phosphorylates MACF1, inhibiting its binding to microtubules which is critical for its role in bulge stem cell migration and skin wound repair (By similarity). Probably regulates NF-kappa-B (NFKB1) at the transcriptional level and is required for the NF-kappa-B-mediated anti-apoptotic response to TNF-alpha (TNF/TNFA) (By similarity). Negatively regulates replication in pancreatic beta-cells, resulting in apoptosis, loss of beta-cells and diabetes (By similarity).
Through phosphorylation of the anti-apoptotic protein MCL1, may control cell apoptosis in response to growth factors deprivation (By similarity). Phosphorylates MUC1 in breast cancer cells, decreasing the interaction of MUC1 with CTNNB1/beta-catenin .
PMID:9819408
Is necessary for the establishment of neuronal polarity and axon outgrowth .
PMID:20067585
Phosphorylates MARK2, leading to inhibition of its activity (By similarity). Phosphorylates SIK1 at 'Thr-182', leading to sustainment of its activity .
PMID:18348280
Phosphorylates ZC3HAV1 which enhances its antiviral activity .
PMID:22514281
Phosphorylates SNAI1, leading to its ubiquitination and proteasomal degradation .
PMID:15448698 PMID:15647282 PMID:25827072 PMID:29059170
Phosphorylates SFPQ at 'Thr-687' upon T-cell activation .
PMID:20932480
Phosphorylates NR1D1 st 'Ser-55' and 'Ser-59' and stabilizes it by protecting it from proteasomal degradation.
Regulates the circadian clock via phosphorylation of the major clock components including BMAL1, CLOCK and PER2 .
PMID:19946213 PMID:28903391
Phosphorylates FBXL2 at 'Thr-404' and primes it for ubiquitination by the SCF(FBXO3) complex and proteasomal degradation (By similarity). Phosphorylates CLOCK AT 'Ser-427' and targets it for proteasomal degradation .
PMID:19946213
Phosphorylates BMAL1 at 'Ser-17' and 'Ser-21' and primes it for ubiquitination and proteasomal degradation .
PMID:28903391
Phosphorylates OGT at 'Ser-3' or 'Ser-4' which positively regulates its activity. Phosphorylates MYCN in neuroblastoma cells which may promote its degradation .
PMID:24391509
Regulates the circadian rhythmicity of hippocampal long-term potentiation and BMAL1 and PER2 expression (By similarity).
Acts as a regulator of autophagy by mediating phosphorylation of KAT5/TIP60 under starvation conditions, activating KAT5/TIP60 acetyltransferase activity and promoting acetylation of key autophagy regulators, such as ULK1 and RUBCNL/Pacer .
PMID:30704899
Negatively regulates extrinsic apoptotic signaling pathway via death domain receptors. Promotes the formation of an anti-apoptotic complex, made of DDX3X, BRIC2 and GSK3B, at death receptors, including TNFRSF10B. The anti-apoptotic function is most effective with weak apoptotic signals and can be overcome by stronger stimulation .
PMID:18846110
Phosphorylates E2F1, promoting the interaction between E2F1 and USP11, stabilizing E2F1 and promoting its activity .
PMID:17050006 PMID:28992046
Phosphorylates mTORC2 complex component RICTOR at 'Ser-1235' in response to endoplasmic stress, inhibiting mTORC2 .
PMID:21343617
Phosphorylates mTORC2 complex component RICTOR at 'Thr-1695' which facilitates FBXW7-mediated ubiquitination and subsequent degradation of RICTOR .
PMID:25897075
Phosphorylates FXR1, promoting FXR1 ubiquitination by the SCF(FBXO4) complex and FXR1 degradation by the proteasome (By similarity).
Phosphorylates interleukin-22 receptor subunit IL22RA1, preventing its proteasomal degradation (By similarity)
PMID:17989220
The receptor then desensitizes rapidly and enters a transient inactive state, characterized by the presence of bound agonist .
PMID:17989220
In the presence of CACNG8, shows resensitization which is characterized by a delayed accumulation of current flux upon continued application of glutamate PMID:21172611
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)
Lithium citrate
Additional database identifiers
Drugs Product Database (DPD)
1399
ChemSpider
12932
HUGO Gene Nomenclature Committee (HGNC)
HGNC:6051
GenAtlas
IMPA2
GeneCards
IMPA2
GenBank Gene Database
AF014398
GenBank Protein Database
2406666
UniProt Accession
IMPA2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:6050
GenAtlas
IMPA1
GeneCards
IMPA1
GenBank Gene Database
X66922
GenBank Protein Database
395340
Guide to Pharmacology
1463
UniProt Accession
IMPA1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:4617
GenAtlas
GSK3B
GeneCards
GSK3B
GenBank Gene Database
L33801
GenBank Protein Database
529237
Guide to Pharmacology
2030
UniProt Accession
GSK3B_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:4573
GenAtlas
GRIA3
GeneCards
GRIA3
GenBank Gene Database
U10302
GenBank Protein Database
507829
Guide to Pharmacology
446
UniProt Accession
GRIA3_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
Wikipedia article
pharmaceutical preparation of the element lithium, used primarily as a psychiatric medication for mood disorders
Read on WikipediaLinked open data from Wikidata (Q152763), 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.