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Meprobamate Tablets 400mg

Document: spc-doc_PL 33414-0058 change

SUMMARY OF PRODUCT CHARACTERISTICS

1    NAME OF THE MEDICINAL PRODUCT

MEPRATE/Meprobamate Tablets 400 mg

2    QUALITATIVE AND QUANTITATIVE    COMPOSITION

Meprobamate BP 400.00 mg

3    PHARMACEUTICAL FORM

Tablets

4    CLINICAL PARTICULARS

4.1    Therapeutic indications

Short term symptomatic treatment of anxiety states where muscle tension is prominent.

4.2    Posology and method of administration

Adults:    The usual dosage is 400 to 1600 mg daily in divided doses.

Higher doses are not recommended.

The    Half the normal adult dose or less may be sufficient for a therapeutic

Elderly:    response in the elderly.

Children:    Not recommended.

Route of administration: oral

Known sensitivity to Meprobamate or related compounds such as carisoprodol or carbromal.

Acute intermittent porphyria.

Patients with a history of alcohol or drug abuse.

Acute pulmonary insufficiency.

Respiratory depression.

Breast-feeding.

4.4 Special warnings and precautions for use

Barbiturate-type dependence may occur particularly when the drug is given in higher than recommended dosages or for long periods. It may also occur on normal therapeutic dosages, particularly in individuals with emotionally unstable personalities or in others prone to alcohol or other drug dependence. Severe withdrawal reactions ranging in severity from tremulousness and insomnia to confusion, delirium tremens, convulsions and occasionally death have occurred. Regular monitoring of treatment and avoidance of routine repeat prescriptions are essential. Treatment should be withdrawn gradually.

Meprobamate may induce seizures in epileptic patients. Caution should be exercised when administering to patients with respiratory disease, muscle weakness, and hepatic and renal impairment.

4.5 Interaction with other medicinal products and other forms of interaction

Like barbiturates, meprobamate causes induction of liver enzymes so that the availability and blood levels of drugs given concurrently that are metabolised by the liver may be affected. These include the following: Coumarin-type anticoagulants; Systemic steroids (including oral contraceptives); Phenytoin; Griseofulvin; Rifampicin; Phenothiazines such as Chlorpromazine; Tricyclic antidepressants.

4.6 Pregnancy and lactation

Meprobamate passes into the breast milk and may cause drowsiness in babies or mothers taking this medicine. Meprobamate has been reported to increase the chance of birth defects if taken during the first three months of pregnancy.

Effects on ability to drive and use machines

4.7


Performance at skilled tasks and alertness may be impaired. Patients should be warned of this hazard and advised not to drive or operate machinery during treatment. These effects are potentiated by alcohol.

4.8 Undesirable effects

Drowsiness and sedation are common adverse effects. Unsteadiness, dizziness, inco-ordination, nausea, vomiting, diarrhoea, constipation, slurred speech, headache, palpitations, arrhythmia, hypotension, syncope, paraesthesiae, weakness, blurred vision, paradoxical excitement, euphoria, tachycardia may occur.

Hypersensitivity reactions have been reported in some 2% of patients, and may occur after a single tablet in patients not previously exposed to the drug. These may include skin reactions or urticaria, itchy maculopapular or erythematous skin rashes, which may be generalised or local.

Severe systemic reactions with shaking chills and fever, nausea, vomiting, hypotension and collapse have occasionally occurred. Blood disorders including thrombocytopenia, non-thrombocytopenic purpura, agranulocytosis, aplastic anaemia and pancytopenia have occurred.

Rarely reported hypersensitivity reactions include: hyperpyrexia, angioneurotic oedema, bronchospasm, oliguria, and anuria. Also, anaphylaxis, erythema multiform, exfoliative dermatitis, stomatitis proctitis, Stevens Johnson syndrome, and bullous dermatitis have been reported.

4.9 Overdose

Poisoning with Meprobamate produces shock, coma, vasomotor and respiratory collapse. Fatal doses have ranged from 12 g to 47.6 g. A regime of forced alkaline diuresis or haemodialysis to reduce blood concentrations of Meprobamate which is rapidly absorbed from the gastro-intestinal tract.

5.1 Pharmacodynamic properties

Meprobamate appears to act at multiple sites in the central nervous system including the thalamus and limbic system.

5.2 Pharmacokinetic properties

Meprobamate is well absorbed from the gastro-intestinal tract. The biotransformation of Meprobamate is hepatic. The plasma half-life is about 10 hours.

Elimination - Meprobamate is excreted in the urine and about 8 - 19% of the drug is excreted unchanged.

5.3 Preclinical safety data

Not applicable

6 PHARMACEUTICAL PARTICULARS

6.1 List of excipients

Maize starch

Pregelatinised Maize Starch Sodium Lauryl Sulphate Sodium Starch Glycollate Magnesium Stearate Purified Water

6.2 Incompatibilities

None known 36 months all pack sizes

6.4    Special precautions for storage

Store below 25°C in a dry place.

Keep container well closed.

Protect from light.

6.5    Nature and contents of container

High density polystyrene with polythene lids and/or polypropylene containers with polypropylene or polythene lids and polyurethane/polythene fillers.

Pack sizes: 100 and 500.

6.6    Special precautions for disposal

No special instructions

7    MARKETING AUTHORISATION HOLDER

Chelonia Healthcare Limited 11 Boumpoulinas Street,

3rd floor, 1060 Nicosia Cyprus

8    MARKETING AUTHORISATION NUMBER(S)

PL 33414/0058

9    DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

25/02/2009

10    DATE OF REVISION OF THE TEXT

25/02/2009