Amisulpride 400mg Tablets
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Amisulpride 400mg Tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 400mg Amisulpride
3 PHARMACEUTICAL FORM
Tablet
White to off-white ovoid shaped film-coated tablets with break line on one side and ‘400’ on other.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Amisulpride 400mg Tablets are indicated for the treatment of acute and chronic schizophrenic disorders, in which positive symptoms (such as delusions, hallucinations, thought disorders) and/or negative symptoms (such as blunted affect, emotional and social withdrawal) are prominent, including patients characterised by predominant negative symptoms.
4.2 Posology and method of administration
For acute psychotic episodes, oral doses between 400 mg/d and 800 mg/d are recommended. In individual cases, the daily dose may be increased up to 1200 mg/d. Doses above 1200 mg/d have not been extensively evaluated for safety and therefore should not be used. No specific titration is required when initiating the treatment with amisulpride. Doses should be adjusted according to individual response.
For patients with mixed positive and negative symptoms, doses should be adjusted to obtain optimal control of positive symptoms.
Maintenance treatment should be established individually with the minimally effective dose.
For patients characterised by predominant negative symptoms, oral doses between 50 mg/d and 300 mg/d are recommended. Doses should be adjusted individually.
Amisulpride can be administered once daily at oral doses up to 300 mg, higher doses should be administered bid.
The minimum effective dose should be used.
Elderly:
Amisulpride should be used with particular caution because of a possible risk of hypotension or sedation.
Children:
Amisulpride is contra-indicated in children under 15 years of age as its safety has not yet been established.
The efficacy and safety of amisulpiride from puberty to the age of 18 years have not been established. There are limited data available on the use of amisulpiride in adolescents in schizophrenia. Therefore, the use of amisulpiride from puberty to the age of 18 years is not recommended.
Renal insufficiency:
Amisulpride is eliminated by the renal route. In renal insufficiency, the dose should be reduced to half in patients with creatinine clearance (CRcL) between 30-60 ml/min and to a third in patients with CRCL between 10-30 ml/min.
As there is no experience in patients with severe renal impairment (CRCL < 10 ml/min) particular care is recommended in these patients (see section 4.4).
Hepatic insufficiency:
Since the drug is weakly metabolised a dosage reduction should not be necessary.
4.3 Contraindications
• Hypersensitivity to the active ingredient or to other ingredients of the drug
• Concomitant prolactin-dependent tumours e.g. pituitary gland prolactinomas
and breast cancer
• Phaeochromocytoma
• Children under 15 years of age
• Pregnancy or lactation
• Women of childbearing potential unless using adequate contraception
• Combination with the following medication which could induce torsades de pointes:
- Class Ia antiarrhythmic agents such as quinidine, disopyramide,
procainamide#
- Class III antiarrhythmic agents such as amiodarone, sotalol
- Other medications such as bepridil, cisapride, sultopride, thioridazine, IV erythromycin, IV vincamine, Halofantrine, pentamidine, sparfloxacin
This list is not exhaustive
• Combination with levodopa (see Section 4.5)
4.4 Special warnings and precautions for use
As with other neuroleptics, Neuroleptic Malignant Syndrome, characterized by hyperthermia, muscle rigidity, autonomic instability, altered consciousness and elevated CPK, may occur. In the event of hyperthermia, particularly with high daily doses, all antipsychotic drugs including Amisulpride should be discontinued.
Hyperglycaemia has been reported in patients treated with some atypical antipsychotic agents, including amisulpride, therefore patients with an established diagnosis of diabetes mellitus or with risk factors for diabetes who are started on amisulpride, should get appropriate glycaemic monitoring.
Amisulpride is eliminated by the renal route. In cases of severe renal insufficiency, the dose should be decreased and intermittent treatment should be considered (see Section 4.2).
Amisulpride may lower the seizure threshold. Therefore patients with a history of epilepsy should be closely monitored during Amisulpride therapy.
In elderly patients, Amisulpride, like other neuroleptics, should be used with particular caution because of a possible risk of hypotension or sedation.
As with other antidopaminergic agents, caution should be also exercised when prescribing Amisulpride to patients with Parkinson's disease since it may cause worsening of the disease. Amisulpride should be used only if neuroleptic treatment cannot be avoided.
Acute withdrawal symptoms including nausea, vomiting and insomnia have very rarely been described after abrupt cessation of high doses of antipsychotic drugs. Recurrence of psychotic symptoms may also occur, and the emergence of involuntary movement disorders (such as akathisa, dystonia and dyskinesia) has been reported. Therefore, gradual withdrawal is advisable.
Prolongation of the QT interval
Amisulpride induces a dose-dependent prolongation of the QT interval. This effect, known to potentiate the risk of serious ventricular arrhythmias such as torsades de pointes is enhanced by the pre-existence of bradycardia, hypokalaemia, congenital or acquired long QT interval. Caution should be exercised when amisulpride is prescribed in patients with known cardiovascular disease or family history of QT prolongation.
Hypokalaemia should be corrected.
Before any administration, and if possible according to the patient's clinical status, it is recommended to monitor factors which could favour the occurrence of this rhythm disorder:
- bradycardia less than 55 bpm,
- hypokalaemia,
- congenital prolongation of the QT interval.
- on-going treatment with a medication likely to produce pronounced bradycardia (<
55 bpm), hypokalaemia, decreased intracardiac conduction, or prolongation of the QTc interval (see Section 4.5).
Caution should be exercised when amisulpride is prescribed in patients with known cardiovascular disease or family history of QT prolongation.
Concomitant antipsychotics should be avoided.
Stroke:
In randomized clinical trials versus placebo performed in a population of elderly patients with dementia and treated with certain atypical antipsychotic drugs, a 3-fold increase of the risk of cerebrovascular events has been observed. The mechanism of such risk increase is not known. An increase in the risk with other antipsychotic drugs, or other populations of patients cannot be excluded. Amisulpride should be used with caution in patients with stroke risk factors.
Increased Mortality in Elderly people with Dementia:
Data from two large observational studies showed that elderly people with dementia who are treated with antipsychotics are at a small increased risk of death compared with those who are not treated. There are insufficient data to give a firm estimate of the precise magnitude of the risk and the cause of the increased risk is not known.
Amisulpride is not licensed for the treatment of dementia-related behavioural disturbances.
Venous thromboembolism:
Cases of venous thromboembolism (VTE) have been reported with antipsychotic drugs. Since patients treated with antipsychotics often present with acquired risk factors for VTE, all possible risk factors for VTE should be identified before and during treatment with Amisulpride and preventive measures undertaken
4.5 Interaction with other Medicinal Products and other forms of Interaction
COMBINATIONS WHICH ARE CONTRAINDICATED Medications which could induce torsades de pointes:
- Class Ia antiarrhythmic agents such as quinidine, dispyramide, procainamide
- Class III antiarrhythmic agents such as amiodarone, sotalol
- Other medications such as bepridil, cisapride, sultopride, thioridazine, IV erythromycin, IV vincamine, Halofantrine, pentamidine, sparfloxacin
This list is not exhaustive
Levodopa: reciprocal antagonism of effects between levodopa and neuroleptics.
COMBINATIONS WHICH ARE NOT RECOMMENDED Amusulpride may enhance the central effects of alcohol COMBINATIONS WHICH REQUIRE PRECAUTIONS FOR USE Medications which enhance the risk of torsades de pointes:
- Bradycardia-inducing medications such as beta-blockers, bradycardia-inducing calcium channel blockers such as diltiazem and verapamil, clonidine, guanfacine; digitalis
- Medications which induce hypokalaemia: hypokalaemic diuretics, stimulant laxatives, IV amphotericin B, glucocortocoids, tetracosactides
- Neuroleptics such as pimozide, haloperidon; imipramine, antidepressants; lithium
COMBINATIONS TO BE TAKEN INTO ACCOUNT
CNS depressants including narcotics, anaesthetics, analgesics, sedative H1 antihistamines, barbiturates, benzodiazepines and other anxiolytic drugs, clonidine and derivatives
Antihypertensive drugs and other hypotensive medications Dopamine agonists (eg: levodopa) since it may attenuate their action
4.6 Fertility, pregnancy and lactation
Pregnancy
In animals, Amisulpride did not show reproductive toxicity. A decrease in fertility linked to the pharmacological effects of the drug (prolactin mediated effect) was observed. No teratogenic effects of Amisulpride were noted.
Very limited clinical data on exposed pregnancies are available. Therefore, the safety of Amisulpride during human pregnancy has not been established.
Use of the drug is not recommended during pregnancy unless the benefits justify the potential risks. If amisulpride is used during pregnancy, neonates may show adverse effects of amisulpride and thus appropriate monitoring should be considered.
For women of childbearing potential, effective contraception should be fully discussed with the physician prior to treatment.
Neonates exposed to antipsychotics including Amisulpride tablets during the third trimester of pregnancy are at risk of adverse reactions including extrapyramidal and/or withdrawal symptoms that may vary in severity and duration following delivery. There have been reports of agitation, hypertonia, hypotonia, tremor, somnolence, respiratory distress, or feeding disorder. Consequently, newborns should be monitored carefully.
Lactation
It is not known whether Solian is excreted in breast milk, breast-feeding is therefore contra-indicated.
4.7 Effects on ability to drive and use machines
Even used as recommended, amisulpride may affect reaction time so that the ability to drive vehicles or operate machinery can be impaired (see Section 4.8).
4.8 Undesirable effects
Adverse effects have been ranked under headings offrequency using the following convention: very common fe.1/10); common fy1/100; <1/10); uncommon (^1/1,000; <1/100); rare (^1/10,000; <1/1,000); very rare (<1/10,000); frequency not known (cannot be estimated from the available data).
Clinical trials data
The following adverse effects have been observed in controlled clinical trials. It should be noted that in some instances it can be difficult to differentiate adverse events from symptoms of the underlying disease.
Nervous system disorders
Very common:
Extrapyramidal symptoms may occur: tremor, rigidity, hypokinesia, hypersalivation, akathisia, dyskinesia. These symptoms are generally mild at optimal dosages and partially reversible without discontinuation of amisulpride upon administration of antiparkinsonian medication. The incidence of extrapyramidal symptoms which is dose related, remains very low in the treatment of patients with predominantly negative symptoms with doses of 50-300mg/day.
Common:
Acute dystonia (spasm torticolis, oculogyric crisis, trismus) may appear. This is reversible without discontinuation of amisulpride upon treatment with an antiparkinsonian agent.
Somnolence.
Uncommon:
Tardive dyskinesia characterised by rhythmic, involuntary movements primarily of the tongue and/or face have been reported, usually after long term administration.
Antiparkinsonian medication is ineffective or may induce aggravation of the symptoms.
Seizures.
Psychiatric disorders
Common:
Insomnia, anxiety, agitation, orgasmic dysfunction.
Gastrointestinal disorders
Common:
Constipation, nausea, vomiting, dry mouth.
Endocrine disorders
Common:
Amisulpride causes an increase in plasma prolactin levels which is reversible after drug discontinuation. This may result in galactorrhoea, amenorrhoea, gynaecomastia, breast pain, and erectile dysfunction.
Metabolism and nutrition disorders
Uncommon:
Hyperglycemia (see 4.4 Special warnings and precautions for use).
Cardiovascular disorders
Common:
Hypotension
Uncommon:
Bradycardia
Investigations
Common:
Weight gain Uncommon:
Elevation of hepatic enzymes, mainly transaminases
Immune system disorders
Uncommon Allergic reaction
Post marketing data
In addition, cases of the following adverse reactions have been reported through spontaneous reporting only:
Nervous system disorders
Frequency not known:
Neuroleptic Malignant Syndrome (see 4.4 Special warnings and precautions for use).
Cardiac disorders
Frequency not known:
Cases of QT prolongation and nd ventricular arrhythmias such as very rare cases of torsades de pointes, ventricular tachycardia, which may result in ventricular fibrillation or cardiac arrest, sudden death (see 4.4 Special warnings and precautions for use).
Vascular disorders
Frequency not known:
Cases of venous thromboembolism, including cases of pulmonary embolism and cases of deep vein thrombosis have been reported with antipsychotic drugs
Skin and subcutaneous tissue disorders
Frequency not known:
Angioedema, urticaria
Pregnancy, puerperium and perinatal conditions
Frequency not known:
Drug withdrawal syndrome neonatal (see 4.6)
4.9 Overdose
Experience with amisulpride in overdosage is limited. Exaggeration of the known pharmacological effects of the drug have been reported. These include drowsiness and sedation, coma, hypotension and extrapyramidal symptoms.
Fatal outcomes have been reported mainly in combination with other psychotropic agents.
In cases of acute overdosage, the possibility of multiple drug intake should be considered.
Since amisulpride is weakly dialysed, hemodialysis should not be used to eliminate the drug.
There is no specific antidote to amisulpride. Appropriate supportive measures should therefore be instituted with close supervision of vital functions including continuous cardiac monitoring due to risk of prolongation of the QT interval until the patient recovers.
If severe extrapyramidal symptoms occur, anticholinergic agents should be administered.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antipsychotics ATC Code: NO5A LO5
Amisulpride binds selectively with a high affinity to human dopaminergic D2/D3 receptor subtypes whereas it is devoid of affinity for D1, D4 and D5 receptor subtypes.
Unlike classical and atypical neuroleptics, amisulpride has no affinity for serotonic, a-adrenergic, histamine H1 and cholinergic receptors. In addition, amisulpride does not bind to sigma sites.
In animal studies, at high doses, amisulpride blocks dopamine receptors located in the limbic structure in preference to those in the striatum.
At low doses it preferentially blocks pre-synaptic D2/D3 receptors, producing dopamine release responsible for its disinhibitory effects.
This pharmacological profile explains the clinical efficacy of amisulpride against both negative and positive symptoms of schizopheria.
5.2 Pharmacokinetic properties
In man, amisulpride shows two absorption peaks: one which is attained rapidly, one hour post-dose and a second between 3 and 4 hours after administration. Corresponding plasma concentrations are 39 ± 3 and 54 ± 4 ng/ml after a 50mg dose.
The volume of distribution is 5.8 l/kg, plasma protein binding is low (16%) and no drug interactions are suspected.
Absolute bioavailability is 48%. Amisulpride is weakly metabolised: two inactive metabolites, accounting for approximately 4% of the dose, have been identified. There is no accumulation of amisulpride and its pharmacokinetics remain unchanged after the administration of repeated doses. The elimination half-life of amisulpride is approximately 12 hours after an oral dose.
Amisulpride is eliminated unchanged in the urine. Fifty percent of an intravenous dose is excreted via the urine, of which 90% is eliminated in the first 24 hours. Renal clearance is in the order of 20 l/h or 330 ml/min.
A carbohydrate rich meal (containing 68% fluids) significantly decreases the AUCs, Tmax and Cmax of amisulpride but no changes were seen after a high fat meal. However, the significance of these findings in routine clinical use is not known.
Hepatic insufficiency: since the drug is weakly metabolised a dosage reduction should not be necessary in patients with hepatic insufficiency.
Renal insufficiency : The elimination half-life is unchanged in patients with renal insufficiency while systemic clearance is reduced by a factor of 2.5 to 3. The AUC of amisulpride in mild renal failure increased two fold and almost tenfold in moderate renal failure (see chapter 4.2). Experience is however limited and there is no data with doses greater than 50 mg.
Amisulpride is very weakly dialysed.
Limited pharmacokinetic data in elderly subjects (> 65 years) show that a 1030 % rise occurs in Cmax, T1/2 and AUC after a single oral dose of 50 mg. No data are available after repeat dosing.
5.3 Preclinical safety data
An overall review of the completed safety studies indicates that amisulpride is devoid of any general, organ-specific, teratogenic, mutagenic or carcinogenic risk. Changes observed in rats and dogs at doses below the maximum tolerated dose are either pharmacological effects or are devoid of major toxicological significance under these conditions. Compared with the maximum recommended dosages in man, maximum tolerated doses are 2 and 7 times greater in the rat (200 mg/kg/d) and dog (120 mg/kg/d) respectively in terms of AUC. No carcinogenic risk, relevant to man, was identified in the rat at up to 1.5 to 4.5 times the expected human AUC.
A mouse carcinogenicity study (120 mg/kg/d) and reproductive studies (160, 300 and 500 mg/kg/d respectively in rat, rabbit and mouse) were performed. The exposure of the animals to amisulpride during these latter studies was not evaluated.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Each tablet contains the following excipients:
Lactose monohydrate
Sodium starch glycollate
Magnesium stearate
Microcrystalline cellulose
Methylcellulose 400cP
Methacrylate polymer
Titanium dioxide (E 171)
Talc
Macrogol 6000
6.2 Incompatibilities
None
6.3 Shelf life
24 months
6.4 Special precautions for storage
Do not store above 25°C. Store in original package.
Nature and contents of container
6.5
The tablets are packed in blisters constituted from a PVC and aluminium foil.
6.6 Special precautions for disposal
None
7 MARKETING AUTHORISATION HOLDER
Milpharm Limited,
Ares,
Odyssey Business Park,
West End Road,
South Ruislip HA4 6QD,
United Kingdom
8 MARKETING AUTHORISATION NUMBER(S)
PL 16363/0148
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
14 May 2004
10 DATE OF REVISION OF THE TEXT
01/05/2012