- lithium citrate tetrahydrate
POM: Prescription only medicine
This information is intended for use by health professionals
Li-Liquid 509mg/5ml Oral Syrup
Lithium Citrate Tetrahydrate
equivalent to Lithium Ion
equivalent to Lithium Carbonate
For the full list of excipients, see section 6.1
Solution for oral administration
• Treatment of mania and hypomania
• Treatment of recurrent bipolar depression, where the use of alternative anti-depressants has been ineffective
• Prophylactic treatment of recurrent affective disorders
• Control of aggressive or self mutilating behaviour
Treatment should be directed to stabilise manic depressive illness rather than to establish early control of acute episodes.
Dosage must be individualised depending on serum lithium levels and clinical response. The dosage necessary to maintain serum lithium levels within the therapeutic range varies from patient to patient. The minimum effective dose should be sought and maintained.
For oral administration only.
A simple treatment schedule has been evolved which except for some minor variations should be followed whether using Li-Liquid therapeutically or prophylactically. The minor variations to this schedule depend on the elements of the illness being treated and these are described later.
1. In patients of average weight (70 kg) an initial total daily dose of 1018 – 3054mg Lithium citrate (equivalent to 400 - 1200mg Lithium carbonate which is 10-30ml of liquid) should be given in divided doses, in the morning and in the evening.
When changing between lithium preparations, serum lithium levels should first be checked, then Li-liquid therapy commenced at a daily dose as close as possible to that of the other form of lithium. As bioavailability varies from product to product (particularly with regard to slow release preparations) a change of product should be regarded as initiation of new treatment.
2. Four to five days after starting treatment (and never longer than one week) a blood sample should be taken for the estimation of serum lithium level. Optimal maintenance serum levels may vary from patient to patient.
3. The objective is to adjust the Li-liquid dose so as to maintain the serum lithium level permanently within the diurnal range of 0.5 – 1.0 mmol/L. Blood samples for measurement of serum lithium concentration should be taken before a dose is due and not less than 12 hours after the previous dose. 'Target' serum lithium concentration at 12 hours should be 0.5 - 0.8 mmol/L. Serum lithium levels should be monitored weekly until stabilisation is achieved. Levels of more than 1.5mmol/L must be avoided.
The liquid should be taken at the same time every day. A double dose to make up for a dose that has been missed should not be taken.
4. Lithium therapy should not be initiated unless adequate facilities for routine monitoring of serum concentrations are available. Following stabilisation of serum lithium levels, the period between subsequent estimations can be increased gradually but should not normally exceed two to three months. Additional measurements should be made following alteration of dosage, on development of intercurrent disease, signs of manic or depressive relapse, following significant changes in sodium or fluid intake, or if signs of lithium toxicity occur.
5. Whilst a high proportion of acutely ill patients may respond within three to seven days after the commencement of therapy with Li-Liquid, it should be continued through any recurrence of the affective disturbance. This is important as the full prophylactic effect may not occur for 6 to 12 months after the initiation of therapy.
6. In patients who show a positive response to therapy with Li-Liquid, treatment is likely to be long term. Careful clinical appraisal of the patient should be exercised throughout medication (see precautions).
7. If lithium is to be discontinued, particularly in cases of high doses, the dose should be reduced gradually.
Prophylactic treatment of recurrent affective disorders: It is recommended that the described treatment schedule is followed.
Treatment of acute mania, hypomania and recurrent bipolar depression: It is likely that a higher than normal intake of Li-Liquid may be necessary during an acute phase. As a general rule the monitoring should maintain serum levels at 0.8 – 1.2 mmol/l until acute symptoms have been controlled. In all other details the described treatment schedule is recommended. The dosage needed may vary from patient to patient. Serum lithium levels should be monitored (see above) and should not exceed 1.5 mmol/l. As soon as control of mania or depression is achieved, the serum lithium level should be determined and it may be necessary, dependent on the results, to lower the dose of Li-Liquid and to re-stabilise serum lithium levels to the prophylactic dose.
Elderly: In elderly patients or those below 50 kg in weight, it is recommended that a starting dose of 509mg lithium citrate (equivalent to 200mg lithium carbonate which is 5ml of liquid) is taken in divided doses, in the morning and in the evening. Elderly patients may be more sensitive to undesirable effects of lithium and may also require lower doses in order to maintain normal serum lithium levels. It follows therefore that long term patients often require a reduction in dosage over a period of years.
Children and adolescents: Not recommended.
In patients with mild and moderate renal insufficiency treated with lithium, serum lithium levels must be closely monitored and the dose should be adjusted accordingly to maintain serum lithium levels within the recommended range (see Section 4.4).
Lithium is contraindicated in patients with severe renal insufficiency (see Section 4.3).
Do not use in patients with a history of hypersensitivity to lithium or to any of the excipients listed in section 6.1, severe renal insufficiency, cardiovascular insufficiency and untreated hypothyroidism.
Lithium should not be given to patients with low body sodium levels, including, for example, dehydrated patients, those on low sodium diets, those with Addison's disease, those with Brugada syndrome or family history of Brugada syndrome.
Do not use in patients who are breastfeeding.
When considering Li-Liquid therapy, it is necessary to ascertain whether patients are receiving lithium in any other form. If so, check serum levels before proceeding.
The minimum clinically effective dose of lithium should always be used (see Section 4.2). Clear instructions regarding the symptoms of impending toxicity should be given by the physician to patients receiving long-term lithium therapy (see Section 4.9). They should be warned of the urgency of immediate action should these symptoms appear, and also of the need to maintain a constant and adequate salt and water intake. At the first sign of toxicity, the patient should consult a physician and lithium levels should be checked. Treatment should be discontinued immediately on the first signs of toxicity (see Section 4.9).
Before starting treatment with lithium, renal function, cardiac function and thyroid function should be evaluated. Patients should be euthyroid before initiation of lithium therapy. Lithium therapy is contraindicated in patients with severe renal insufficiency or cardiac insufficiency (see Section 4.3).
Renal, cardiac and thyroid functions should be re-assessed regularly during treatment with lithium.
For monitoring recommendations of lithium serum levels see Section 4.2.
Since lithium is primarily excreted via the renal route, significant accumulation of lithium may occur in patients with renal insufficiency. Therefore, if patients with mild or moderate renal impairment are being treated with lithium, serum lithium levels should be closely monitored (see Section 4.2) and the dose should be adjusted accordingly. If very regular and close monitoring of serum lithium levels and plasma creatinine levels is not possible, lithium should not be prescribed in this population. Lithium is contraindicated in patients with severe renal insufficiency (see Section 4.3).
The possibility of hypothyroidism and renal dysfunction arising during prolonged treatment should be borne in mind and periodic assessments made.
Patients should be warned to report if polyuria or polydipsia develop. In patients who develop polyuria and/or polydipsia (see Section 4.8), renal function should be monitored in addition to the routine serum lithium assessment.
Renal tumours: Cases of microcysts, oncocytomas and collecting duct renal carcinoma have been reported in patients with severe renal impairment who received lithium for more than 10 years (see Section 4.8).
If episodes of nausea, vomiting, diarrhoea, excessive sweating, and/or other conditions leading to salt/water depletion (including severe dieting) occur, lithium dosage should be closely monitored and dosage adjustments made as necessary. Drugs likely to upset electrolyte balance such as diuretics should also be reported. Indeed, sodium depletion increases the lithium plasma concentration (due to competitive reabsorption at the renal level). In these cases, lithium dosage should be closely monitored and reduction of dosage may be necessary.
Caution should be exercised to ensure that diet and fluid intake are normal in order to maintain a stable electrolyte balance. This may be of special importance in very hot weather or work environment. Infectious diseases including colds, influenza, gastro-enteritis and urinary infections may alter fluid balance and thus affect serum lithium levels. Treatment discontinuation should be considered during any intercurrent infection.
Risk of convulsions
The risk of convulsions may be increased in case of co-administration of lithium with drugs that lower the epileptic threshold, or in epileptic patients (see sections 4.5 and 4.8).
Benign intracranial hypertension
There have been case reports of benign intracranial hypertension (see Section 4.8). Patients should be warned to report persistent headache and/or visual disturbances.
As a precautionary measure, lithium should be avoided in patients with congenital long QT syndrome, and caution should be exercised in patients with risk factors such as QT interval prolongation (e.g. uncorrected hypokalaemia, bradycardia), and in patients concomitantly treated with drugs that are known to prolong the QT interval (see Sections 4.5 and 4.8).
Lithium may unmask or aggravate Brugada syndrome, a hereditary disease of the cardiac sodium channel with characteristic electrocardiographic changes (right bundle branch block and ST segment elevation in right precordial leads), which may lead to cardiac arrest or sudden death. Lithium should not be administered to patients with Brugada Syndrome or a family history of Brugada Syndrome (see Section 4.3). Caution is advised in patients with a family history of cardiac arrest or sudden death.
Elderly patients are particularly liable to lithium toxicity and may exhibit adverse reactions at serum levels ordinarily tolerated by younger patients. Caution is also advised since lithium excretion may be reduced in the elderly due to age related disease in renal function (see Sections 4.2 and 5.2).
The use in children is not recommended.
Excipients in the Formulation
Li -lithium 509mg/5ml Oral Syrup contains methyl and propyl hydroxybenzoates (preservatives) which may cause allergic reactions (possibly delayed).
The medicine contains 1.7g of glucose in each 5ml. When taken according to dosage recommendations, the maximum dose supplies up to 10.2g of glucose.
It also contains 0.4g of sorbitol. When taken according to dosage recommendations, the maximum dose supplies up to 2.2g of sorbitol. It is unsuitable for those with an hereditary fructose intolerance.
The flavour contains a small amount of ethanol (alcohol), less than 100mg per dose.
If one of the following drugs is initiated, lithium dosage should either be adjusted or concomitant treatment stopped, as appropriate.
Interactions which increase lithium concentrations
• Metronidazole may reduce lithium renal clearance.
• Non-steroidal anti-inflammatory drugs including selective cyclo-oxygenase (COX) 2 inhibitors (monitor serum lithium concentrations more frequently if NSAID therapy is initiated or discontinued)
• ACE inhibitors
• Angiotensin II receptor antagonists.
• Diuretics (thiazides show a paradoxical antidiuretic effect resulting in possible water retention and lithium intoxication). Should be prescribed with extreme caution and careful monitoring. Similar precautions should be exercised on diuretic withdrawal. Note that thiazides show a paradoxical antidiuretic effect resulting in possible water retention and lithium intoxication. If a thiazide diuretic has to be prescribed for a lithium-treated patient, lithium dosage should first be reduced and the patient re-stabilised with frequent monitoring. Similar precautions should be exercised on diuretic withdrawal. Loop diuretics seem less likely to increase lithium levels.
• Other drugs affecting electrolyte balance, e.g. steroids, may alter lithium excretion and therefore should be avoided.
Interactions which decrease serum lithium concentrations
Serum lithium levels may be decreased due to an increase in lithium renal clearance in case of concomitant administration of one of the following drugs:
• xanthines (such as caffeine and theophylline)
• sodium bicarbonate containing products
• Diuretics (osmotic and carbonic anhydrase inhibitors)
Interactions causing neurotoxicity
• Neuroleptics (particularly haloperidol at higher dosages), flupentixol, risperidone, diazepam, thioridazine, fluphenazin, chlorpromazine and clozapine may lead in rare cases to neurotoxicity in the form of confusion, disorientation, lethargy, tremor, extrapyramidal symptoms and myoclonus. Co-administration of lithium with neuroleptics increases the risk of Neuroleptic Malignant Syndrome (NMS), which may be fatal. Discontinuation of both drugs is recommended at the first signs of neurotoxicity.
• Triptan derivatives and/or serotonergic antidepressants such as Selective Serotonin Re-uptake Inhibitors (e.g. fluvoxamine and fluoxetine) as this combination may precipitate a serotonergic syndrome, which justifies immediate discontinuation of treatment.
• Calcium channel blockers may lead to a risk of neurotoxicity in the form of ataxia, confusion and somnolence, reversible after discontinuation of the drug. Lithium concentrations may be increased.
• Carbamazepine may lead to dizziness, somnolence, confusion and cerebellar symptoms such as ataxia.
• Tri-cyclic antidepressants
Caution is advised if lithium is co-administered with other drugs that prolong the QT interval (see Sections 4.4 and 4.8), e.g. Class IA (e.g. quinidine, disopyramide), or Class III (e.g. amiodarone) antiarrhythmic agents, cisapride, antibiotics such as erythromycin, antipsychotics such as thioridazine or amisulpride. The list is not comprehensive.
Caution is advised if lithium is co-administered with drugs that lower the epileptic threshold (see Section 4.4), e.g. antidepressants such as SSRIs, tricyclic antidepressants, antipsychotics, anaesthetics, theophylline. The list is not comprehensive.
Lithium may prolong the effects of neuromuscular blocking agents. There have been reports of interaction between lithium and phenytoin, indometacin and other prostaglandin-synthetase inhibitors.
Raised plasma levels of ADH may occur during treatment.
Serotonin syndrome is a potentially life-threatening adverse reaction, which is caused by an excess of serotonin (e.g. from overdose or concomitant use of serotonergic drugs), necessitating hospitalisation and even causing death.
Symptoms may include:
- Mental status changes (agitation, confusion, hypomania, eventually coma)
- Neuromuscular abnormalities (myoclonus, tremor, hyperreflexia, rigidity, akathisia)
- Autonomic hyperactivity (hypo or hypertonia, tachycardia, shivering, hyperthermia, diaphoresis)
- Gastrointestinal symptoms (diarrhoea)
Strict adherence to the recommended doses is an essential factor for the prevention of the occurrence of this syndrome.
Lithium therapy should not be used during pregnancy, especially during the first trimester, unless considered essential. There is epidemiological evidence that lithium may be harmful to the foetus in human pregnancy. Lithium crosses the placental barrier. In animal studies lithium has been reported to interfere with fertility, gestation and foetal development. An increase in cardiac and other abnormalities, especially Ebstein anomaly, have been reported. Therefore, a pre-natal diagnosis such as ultrasound and electrocardiogram examination is strongly recommended. In certain cases where a severe risk to the patient could exist if treatment were stopped, lithium has been continued during pregnancy.
It is strongly recommended that lithium be discontinued before a planned pregnancy. If it is considered essential to maintain treatment with Li-Liquid during pregnancy, serum lithium levels should be monitored closely since renal function changes gradually during pregnancy and suddenly at parturition, requiring dosage adjustments. It is recommended that administration of Li-Liquid be discontinued shortly before delivery and recommenced a few days post-partum.
Neonates may show signs of lithium toxicity including symptoms such as lethargy , flaccid muscle tone, or hypotonia. Careful clinical observation of the neonate exposed to lithium during pregnancy is recommended and lithium levels may need to be monitored as necessary.
Women of child-bearing potential
It is advisable that women treated with lithium should adopt adequate contraceptive methods.
Lithium is secreted in breast milk therefore bottle feeding is recommended. (See section 4.3 Contraindications).
There have been case reports of neonates showing signs of lithium toxicity (see Pregnancy). Therefore lithium should not be used during breast-feeding (see Section 4.3). A decision should be made whether to discontinue lithium therapy or to discontinue breast-feeding, taking into account the importance of the drug to the mother and the importance of breast-feeding to the infant.
Lithium may cause disturbances of the CNS. Since lithium may slow reaction time, and considering the adverse reactions profile of lithium (see Section 4.8), patients should be warned of the possible hazards when driving or operating machinery.
Side effects are usually related to serum lithium concentration and are less common in patients with plasma lithium concentrations below 1.0 mmol/L. The adverse reactions usually subside with a temporary reduction or discontinuation of lithium treatment.
Mild gastrointestinal effects such as nausea, a general discomfort and vertigo, may occur initially, but frequently disappear after the first few days of lithium administration.
Fine tremor of the hands, polyuria and thirst and nausea may occur.
Blood and lymphatic system disorders:
Euthyroid goitre, hypothyroidism, hyperthyroidism, hyperparathyroidism, thyrotoxicosis. Lithium induced hypothyroidism may be managed successfully with concomitant thyroxine.
Metabolism and nutrition disorders:
Hyperglycaemia, hypercalcaemia, hypermagnesaemia, weight gain.
Nervous system disorders:
Ataxia, peripheral sensorimotor neuropathy, hyperactive deep tendon reflexes, extrapyramidal symptoms, seizures, slurred speech, dizziness, stupor, coma, pseudotumor cerebri, myasthenia gravis, giddiness, dazed feeling, memory impairment, tremor, especially fine hand tremors, dysarthria, myoclonus, benign intracranial hypertension (see section 4.4), vertigo, impaired consciousness, abnormal reflexes, convulsions (see sections 4.4 and 4.5), encephalopathy, cerebellar syndrome (usually reversible), nystagmus.
The above symptoms may result in fall.
Peripheral neuropathy may occur on long-term treatment and is usually reversible at cessation of lithium.
Scotomata, blurred vision.
Reported cardiovascular effects are cardiac arrhythmia, bradycardia, sinus node dysfunction, peripheral circulatory collapse, hypotension, oedema, Raynaud's phenomenon and ECG changes, such as reversible flattening or inversion of T-waves and QT prolongation, (see sections 4.4 and 4.5), AV block, cardiomyopathy.
Anorexia, nausea, vomiting, diarrhoea, gastritis, excessive salivation, dry mouth, abdominal discomfort, taste disorder.
Skin and subcutaneous tissue disorders:
Alopecia, acne, folliculitis, pruritus, exacerbation or occurrence of psoriasis, allergic rashes, acneiform eruptions, papular skin disorder, cutaneous ulcers.
Frequency not known: lichenoid drug reaction.
Musculoskeletal and connective tissue disorder:
Muscle weakness, rhabdomyolysis, arthralgia, myalgia, myoclony and abnormal reflex
Renal and urinary disorders:
Polydipsia and/or polyuria, symptoms of nephrogenic diabetes insipidus, histological renal changes with interstitial fibrosis after long term treatment have been reported (see section 4.4). This is usually reversible on lithium withdrawal.
Long-term treatment with lithium may result in permanent changes in kidney histology and impairment of renal function.
High serum concentrations of lithium including episodes of acute lithium toxicity may aggravate these changes. The minimum clinically effective dose of lithium should always be used. In patients who develop polyuria and/or polydipsia, renal function should be monitored, e.g. with measurement of blood urea, serum creatinine and urinary protein levels in addition to the routine serum lithium assessment.
Rare cases of nephrotic syndrome have been reported.
Frequency unknown: microcysts, oncocytoma and collecting duct renal carcinoma (in long-term therapy) (see Section 4.4).
Reproductive system disorders:
General disorders and administration site conditions:
Peripheral oedema and urticaria attributed to some excipients.
If any of the above symptoms appear, treatment should be stopped immediately and arrangements made for serum lithium measurement.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Any overdose in a patient who has been taking chronic lithium therapy should be regarded as potentially serious.
In patients with a raised lithium concentration, the risk of toxicity is greater in those with the following underlying medical conditions: hypertension; diabetes; congestive heart failure; chronic renal failure; schizophrenia; Addison's disease.
A single acute overdose usually carries low risk and patients tend to show mild symptoms only, irrespective of their serum lithium concentration. However more severe symptoms may occur after a delay if lithium elimination is reduced because of renal impairment, particularly if a slow-release preparation has been taken. The fatal dose, in a single overdose, is probably over 5g.
If an acute overdose has been taken by a patient on chronic lithium therapy, this can lead to serious toxicity occurring even after a modest overdose as the extravascular tissues are already saturated with lithium.
Lithium toxicity can also occur in chronic accumulation for the following reasons:Acute or chronic overdosage; dehydration e.g. due to intercurrent illness, deteriorating renal function, drug interactions, most commonly involving a thiazide diuretic or a non-steroidal anti-inflammatory drug (NSAID).
The onset of symptoms may be delayed, with peak effects not occurring for as long as 24 hours, especially in patients who are not receiving chronic lithium therapy or following the use of a sustained release preparation.
Symptoms of lithium intoxication include:
Mild: Nausea, diarrhoea, blurred vision, polyuria, light headedness, fine resting tremor, muscular weakness and drowsiness.Moderate: Increasing confusion, blackouts, fasciculation and increased deep tendon reflexes, myoclonic twitches and jerks, choreoathetoid movements, urinary or faecal incontinence, increasing restlessness followed by stupor. Hypernatraemia. Severe: Coma, convulsions, cerebellar signs, cardiac dysrhythmias including sino-atrial block, sinus and junctional bradycardia and first degree heart block. Hypotension or rarely hypertension, circulatory collapse and renal failure.
Gastrointestinal disorders: increasing anorexia and vomiting.
Nervous system disorders: Encephalopathy, cerebellar syndrome with symptoms such as muscle weakness, lack of coordination, drowsiness or lethargy, giddiness, ataxia, nystagmus, coarse tremor. Tinnitus, dysarthria, twitching, myoclonus, extrapyramidal disorders.
ECG changes (flat or inverted T waves, QT prolongation), AV block, dehydration and electrolyte disturbances.
At blood levels above 2-3 mmol/l, there may be a large output of dilute urine and renal insufficiency, with increasing confusion, convulsions, coma and death.
There is no specific antidote to lithium. In the event of lithium overdose, lithium should be discontinued and serum levels monitored closely. Diuretics should not be used (see section 4.5). All patients should be observed for a minimum of 24 hours. ECG should be monitored in symptomatic patients. Steps should be taken to correct hypotension. Supportive treatment should be initiated, which includes correction of fluid and electrolyte balance, if necessary.
Consider gastric lavage for non-sustained-release preparations if more than 4 g has been ingested by an adult within one hour or definite ingestion of a significant amount by a child. Slow-release tablets do not disintegrate in the stomach and most are too large to pass up a lavage tube. Gut decontamination is not useful for chronic accumulation. Activated charcoal does not adsorb lithium.
Haemodialysis is the treatment of choice for severe lithium intoxication (especially in patients manifesting with severe nervous system disorders) or in cases of overdose accompanied by renal impairment. Haemodialysis should be continued until there is no lithium in the serum or dialysis fluid.
Serum lithium levels should be monitored for at least a further week to take account of any possible rebound in serum lithium levels as a result of delayed diffusion from the body tissues.
In cases of acute on chronic overdose or in cases of chronic lithium toxicity if the lithium concentration is >4.0 mmol/L, discuss with your local poisons service.Clinical improvement generally takes longer than reduction of serum lithium concentrations regardless of the method used.
ATC Code: N05A N01
Although lithium is a simple ion it can exert a profound effect on both human behaviour and early embryonic development. Manic depressive psychosis, characterised by dramatic savings in mood can be effectively controlled.
Little is known about the way the lithium ion can modify neurotransmission within the CNS. Many of the proposed mechanisms have suggested an inhibitory effect on components of various neurotransmitter signalling pathways, such as cyclic AMP formation, cyclic GMP formation, G-proteins or inositol phosphate metabolism.
Lithium is rapidly and completely absorbed from the gastrointestinal tract when taken in solution as one of its salts.
Peak plasma concentrations are obtained about 0.75 hours after ingestion of Li-Liquid. Lithium is reported to have a plasma half life of about 7 to 20 hours during the daytime. Lithium is excreted by the kidneys. There is a narrow margin between the therapeutic and the toxic plasma concentration. Therefore, not only is individual titration of lithium dosage essential to ensure constant plasma concentrations for the patient involved, but the conditions under which the blood samples are taken for monitoring must be carefully controlled. In practice a blood sample drawn 12 hours after the last dose of lithium in a patient who has been taking his daily lithium requirement at the scheduled hours during the past 48 hours is measured. Under such conditions the usual therapeutic plasma concentrations of lithium are 0.6 - 1.25 mmol/L, with a reported effective range of 0.5 - 1.5mmol/L
There is epidemiological evidence that lithium may be harmful to the foetus in human pregnancy. Therefore it is recommended that lithium be discontinued or if the lithium is necessary, the levels in the patient should be monitored closely.
Lithium is a drug on which extensive clinical experience has been obtained. Relevant information for the prescriber is provided elsewhere in the Summary of Product Characteristics.
Citric acid monohydrate, saccharin sodium, sorbitol solution, syrup liquid glucose, propylene glycol, methyl and propyl hydroxybenzoate, colouring E104, cherry flavour (containing ethanol and propylene glycol) and purified water
6 months opened
Store above 4°C and protect from light.
Amber (Type III) glass bottles with capacity of 150ml.
HDPE EPE wadded, tamper evident, child resistant.
Keep out of the sight and reach of children.
Rosemont Pharmaceuticals Ltd
Yorkdale Industrial Park
27 January 1992
Rosemont House, Yorkdale Industrial Park, Braithwaite Street, Leeds, Yorkshire, LS11 9XE
+44 (0)113 244 1400
+44 (0)800 919 312
+44 (0)113 245 3567
+44 (0)7836 557 879