Prochlorperazine 3 mg Buccal Tablets

Alliance Pharmaceuticals🇬🇧 Electronic Medicines Compendium

Approval Date: N/A
Approval ID: e1361d5650541843
Company: Alliance Pharmaceuticals
Type: Standard

Approval Details

Approval Id: e1361d5650541843
Drug Approval Emc Name: Prochlorperazine 3 mg Buccal Tablets
Drug Name: Prochlorperazine 3 mg Buccal Tablets
Company Name: Alliance Pharmaceuticals
Company Address: Avonbridge House, Bath Road, Chippenham, Wiltshire, SN15 2BB
Company Website: http://www.alliancepharma.co.uk
Company Telephone: +44 (0)1249 466 966
Company Medical Info Email: medinfo@alliancepharma.co.uk
Atc Code: N05AB
Legal Category: Prescription only medicine
Authorisation Holder: Alliance Pharmaceuticals Limited Avonbridge House Bath Road Chippenham Wiltshire SN15 2BB
Authorisation Number: Buccastem 3 mg Buccal Tablets, Prochlorperazine 3 mg Buccal Tablets PL 16853/0101
Authorisation Date: 16th February 2010
Instruction Authorisation Holder: Alliance Pharmaceuticals Limited Avonbridge House Bath Road Chippenham Wiltshire SN15 2BB
Instruction Authorisation Number: Buccastem 3 mg Buccal Tablets, Prochlorperazine 3 mg Buccal Tablets PL 16853/0101
Instruction Authorisation Date: 16th February 2010
Instruction Composition: Each buccal tablet contains 3.0 mg prochlorperazine maleate. \*\*Excipients with known effect:\*\* Compressible sugar (contains sucrose) 49.493 mg
Instruction Dosage Form: Buccal tablet.
Instruction Clinical Particulars: 4.1 Therapeutic indications Symptomatic treatment of vertigo due to Ménière's Disease, Labyrinthitis and other causes. For nausea and vomiting from whatever cause. In the treatment of migraine.4.2 Posology and method of administration To be placed in the buccal cavity, high up along the top gum under the upper lip, until dissolved. Do not chew or swallow the tablet. Adults and children aged 12 years and over: One or two tablets twice a day. Children under 12 years: Not recommended. Elderly patients: There is no evidence that dosage need be modified for the elderly.4.3 Contraindications • Hypersensitivity to the active substance or to any of the excipients listed in section 6.1 • Impaired liver function • Existing blood dyscrasias • Epilepsy • Parkinson's Disease • Prostatic hypertrophy • Narrow angle glaucoma4.4 Special warnings and precautions for use Buccastem/Prochlorperazine 3 mg Buccal Tablets should be avoided in patients with stroke risk factors and myasthenia gravis. Agranulocytosis has been reported with phenothiazines. The occurrence of unexplained infections or fever may be evidence of blood dyscrasia (see section 4.8), and requires immediate haematological investigation. It has been reported that patients with AIDS may be particularly susceptible to antipsychotic-induced extrapyramidal effects. Because of the risk of photosensitisation, patients should be advised to avoid exposure to direct sunlight and use sunscreen (see section 4.8). Hypotension, usually postural, may occur, particularly in elderly or volume depleted patients. Nausea and vomiting as a sign of organic disease may be masked by the anti-emetic action. Neuroleptic malignant syndrome (NMS) is a potentially fatal symptom complex associated with antipsychotic medicinal products. Alteration in mental status and other neurological signs often precede systemic signs of NMS. It is imperative that treatment be discontinued in the event of NMS (characterised by unexplained fever, hyperthermia, autonomic dysfunction, altered consciousness, muscle rigidity) (see section 4.8). 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, and preventive measures undertaken (see section 4.8). \*\*\*\*QT prolongation\*\*\*\* Neuroleptic phenothiazines may potentiate QT interval prolongation which increases the risk of onset of serious ventricular arrhythmias of the torsade de pointes type, which is potentially fatal. Buccastem/Prochlorperazine 3mg Buccal Tablets should be used with caution in patients with congenital or documented acquired QT prolongation and/or known risk factors for prolongation of the QT interval such as: - cardiac disease e.g. heart failure, myocardial infarction - proarrhythmic conditions e.g bradycardia (< 50 bpm) - a history of ventricular dysrhythmias - uncorrected hypokalemia and/or hypomagnesemia - and during concomitant administration with QT interval prolonging drugs (see section 4.5). If signs of cardiac arrhythmia occur during treatment with Buccastem/Prochlorperazine 3 mg Buccal Tablets, treatment should be stopped and an ECG should be performed. \*\*\*\*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. Buccastem/Prochlorperazine 3mg Buccal Tablets is not licensed for the treatment of dementia-related behavioural disturbances. Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrose-isomaltase insufficiency should not take this medicine.4.5 Interaction with other medicinal products and other forms of interaction Alcohol and CNS depressants should be used with caution due to the possible additive CNS depressant effect. The hypotensive effect of antihypertensive drugs may be exaggerated. The mild anticholinergic effect of neuroleptics may be enhanced by other anticholinergic drugs. Anticonvulsants – efficacy may be diminished necessitating dosage adjustment, as prochlorperazine may lower the seizure threshold. The concomitant use of lithium may result in severe extrapyramidal side effects or severe neurotoxicity. The concurrent use of desferrioxamine and prochlorperazine should be avoided. There is an increased risk of arrhythmias when neuroleptics are used with concomitant QT prolonging drugs (including certain anti-arrhythmics, antidepressants, macrolide antibiotics and other antipsychotics) and drugs causing electrolyte imbalance (see section 4.4).4.6 Fertility, pregnancy and lactation There is inadequate evidence of the safety in human pregnancy. Buccastem/Prochlorperazine 3 mg Buccal Tablets should be avoided unless absolutely necessary during the first trimester of pregnancy. Since data from animal studies show that prochlorperazine may be found in breast milk it should not be used during lactation. Neonates exposed to antipsychotics (including prochlorperazine) 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.4.7 Effects on ability to drive and use machines Patients who drive or operate machinery should be warned of the possibility of drowsiness.4.8 Undesirable effects Undesirable effects are listed by MedDRA System Organ Classes. Assessment of undesirable effects is based on the following frequency groupings: Very common: ≥1/10 Common: ≥1/100 to <1/10 Uncommon: ≥1/1,000 to <1/100 Rare: ≥1/10,000 to <1/1,000 Very rare: <1/10,000 Not known: cannot be estimated from the available data \*\*Tabulated list of adverse reactions\*\* | | | | --- | --- | | \*\*System organ class\*\* | \*\*Undesirable effect and frequency\*\* | | Blood and lymphatic system disorders | \*Rare:\* Blood dyscrasia | | Immune system disorders | \*Not known:\* Hypersensitivity reactions such as rash and angioedema | | Endocrine disorders | \*Very rare:\* Hyperprolactinaemia which may result in gynaecomastia, galactorrhoea and amenorrhoea | | Metabolism and nutrition disorders | \*Not known:\* Hyponatraemia Syndrome of inappropriate antidiuretic hormone secretion Hyperglycaemia Glucose tolerance impaired | | Psychiatric disorders | \*Not known:\* Insomnia Agitation | | Nervous system disorders | \*Not known:\* Convulsion Drowsiness Dizziness Extrapyramidal reactions including acute dystonia, akathisia, parkinsonism and tardive dyskinesia | | Cardiac disorders | \*Not known:\* Arrythmia\\* QT prolongation\\* | | Vascular disorders | \*Not known:\* Hypotension (usually orthostatic) | | Gastrointestinal disorders | \*Not known:\* Dry mouth Irritation gum Mouth irritation Hypoaesthesia oral Paraesthesia oral Taste disorders | | Hepatobiliary disorders | \*Rare:\* Jaundice \*Not known:\* Cholestasis | | Skin and subcutaneous tissue disorders | \*Not known:\* Skin reaction Photosensitivity (see section 4.4) | | Pregnancy, puerperium and perinatal conditions | \*Not known:\* Drug withdrawal syndrome neonatal (see Section 4.6) | \\* See 'Description of selected adverse reactions' \*\*\*\*Description of selected adverse reactions\*\*\*\* Impotence, ejaculation disorder, priapism, and agranulocytosis (see section 4.4) are class effects associated with phenothiazines. Neuroleptic malignant syndrome may occur with any neuroleptic (see section 4.4). Cases of venous thromboembolism, including cases of pulmonary embolism and cases of deep vein thrombosis have been reported with antipsychotic drugs- Frequency unknown (see section 4.4). QT prolongation, cardiac arrhythmias, including ventricular arrhythmias which may result in ventricular fibrillation or cardiac arrest have been reported during neuroleptic phenothiazine therapy. Pre-existing cardiac disease, proarrhythmic conditions, hypokalaemia, hypomagnesemia, or concomitant administration with QT interval prolonging drugs may predispose. \*\*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.4.9 Overdose The signs and symptoms will be predominantly extrapyramidal and may be accompanied either by restlessness and agitation or central nervous depression. Hypotension may also occur. Treatment is essentially symptomatic and supportive. There is no specific antidote. Do not induce vomiting. Particular attention must be directed to maintaining a clear airway since this may be threatened by extrapyramidal muscle dystonias. Severe dystonic reactions usually respond to procyclidine or orphenadrine given i.m. or i.v. If convulsions occur they should be treated using i.v. diazepam. If hypotension is present, strict attention to ventilation and posturing of the patient will often secure the desired effect, but failing this, consideration should be given to volume expansion by i.v. fluids. If this is insufficient, positive inotropic agents such as dopamine may be tried, but peripheral vasoconstrictor agents are not generally recommended. Adrenaline should \*\*NOT\*\* be used.
Instruction Pharmacology: 5.1 Pharmacodynamic properties Pharmacotherapeutic group: Phenothiazines with piperazine structure ATC code: N05AB Prochlorperazine is a member of the phenothiazine group of neuroleptics which, in doses lower than those used in psychiatry, is usually employed for its anti-emetic properties. The site of action is thought to be the chemoreceptor trigger zone.5.2 Pharmacokinetic properties The buccal tablets are placed in the buccal cavity where they form a gel from which the prochlorperazine is released and absorbed. The plasma levels achieved at steady-state on a dosage regimen of one buccal tablet twice daily are similar to those observed with the standard oral dosage of one 5 mg tablet taken three times daily. The elimination half-life of prochlorperazine in this formulation is 9.0 hours, similar to that observed with the oral formulation.5.3 Preclinical safety data No preclinical findings of relevance have been reported.
Instruction Pharmaceutical Particulars: 6.1 List of excipients Compressible sugar, povidone K30, xanthan gum, locust bean gum, talc, magnesium stearate and riboflavin sodium phosphate.6.2 Incompatibilities None.6.3 Shelf life Three years for blister packs. Two years for plastic tubs.6.4 Special precautions for storage Protect from light.6.5 Nature and contents of container 250 micron PVC/PVdC aluminium foil blister packs or plastic tubs. Pack size: Blister packs of 2, 8, 15, 30, 50, or 60 tablets. Plastic tubs of 250 tablets.6.6 Special precautions for disposal and other handling No special requirements.
Instruction Content: ## Composition Each buccal tablet contains 3.0 mg prochlorperazine maleate. \*\*Excipients with known effect:\*\* Compressible sugar (contains sucrose) 49.493 mg ## Pharmaceutical Form Buccal tablet. ## Clinical Particulars 4.1 Therapeutic indications Symptomatic treatment of vertigo due to Ménière's Disease, Labyrinthitis and other causes. For nausea and vomiting from whatever cause. In the treatment of migraine.4.2 Posology and method of administration To be placed in the buccal cavity, high up along the top gum under the upper lip, until dissolved. Do not chew or swallow the tablet. Adults and children aged 12 years and over: One or two tablets twice a day. Children under 12 years: Not recommended. Elderly patients: There is no evidence that dosage need be modified for the elderly.4.3 Contraindications • Hypersensitivity to the active substance or to any of the excipients listed in section 6.1 • Impaired liver function • Existing blood dyscrasias • Epilepsy • Parkinson's Disease • Prostatic hypertrophy • Narrow angle glaucoma4.4 Special warnings and precautions for use Buccastem/Prochlorperazine 3 mg Buccal Tablets should be avoided in patients with stroke risk factors and myasthenia gravis. Agranulocytosis has been reported with phenothiazines. The occurrence of unexplained infections or fever may be evidence of blood dyscrasia (see section 4.8), and requires immediate haematological investigation. It has been reported that patients with AIDS may be particularly susceptible to antipsychotic-induced extrapyramidal effects. Because of the risk of photosensitisation, patients should be advised to avoid exposure to direct sunlight and use sunscreen (see section 4.8). Hypotension, usually postural, may occur, particularly in elderly or volume depleted patients. Nausea and vomiting as a sign of organic disease may be masked by the anti-emetic action. Neuroleptic malignant syndrome (NMS) is a potentially fatal symptom complex associated with antipsychotic medicinal products. Alteration in mental status and other neurological signs often precede systemic signs of NMS. It is imperative that treatment be discontinued in the event of NMS (characterised by unexplained fever, hyperthermia, autonomic dysfunction, altered consciousness, muscle rigidity) (see section 4.8). 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, and preventive measures undertaken (see section 4.8). \*\*\*\*QT prolongation\*\*\*\* Neuroleptic phenothiazines may potentiate QT interval prolongation which increases the risk of onset of serious ventricular arrhythmias of the torsade de pointes type, which is potentially fatal. Buccastem/Prochlorperazine 3mg Buccal Tablets should be used with caution in patients with congenital or documented acquired QT prolongation and/or known risk factors for prolongation of the QT interval such as: - cardiac disease e.g. heart failure, myocardial infarction - proarrhythmic conditions e.g bradycardia (< 50 bpm) - a history of ventricular dysrhythmias - uncorrected hypokalemia and/or hypomagnesemia - and during concomitant administration with QT interval prolonging drugs (see section 4.5). If signs of cardiac arrhythmia occur during treatment with Buccastem/Prochlorperazine 3 mg Buccal Tablets, treatment should be stopped and an ECG should be performed. \*\*\*\*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. Buccastem/Prochlorperazine 3mg Buccal Tablets is not licensed for the treatment of dementia-related behavioural disturbances. Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrose-isomaltase insufficiency should not take this medicine.4.5 Interaction with other medicinal products and other forms of interaction Alcohol and CNS depressants should be used with caution due to the possible additive CNS depressant effect. The hypotensive effect of antihypertensive drugs may be exaggerated. The mild anticholinergic effect of neuroleptics may be enhanced by other anticholinergic drugs. Anticonvulsants – efficacy may be diminished necessitating dosage adjustment, as prochlorperazine may lower the seizure threshold. The concomitant use of lithium may result in severe extrapyramidal side effects or severe neurotoxicity. The concurrent use of desferrioxamine and prochlorperazine should be avoided. There is an increased risk of arrhythmias when neuroleptics are used with concomitant QT prolonging drugs (including certain anti-arrhythmics, antidepressants, macrolide antibiotics and other antipsychotics) and drugs causing electrolyte imbalance (see section 4.4).4.6 Fertility, pregnancy and lactation There is inadequate evidence of the safety in human pregnancy. Buccastem/Prochlorperazine 3 mg Buccal Tablets should be avoided unless absolutely necessary during the first trimester of pregnancy. Since data from animal studies show that prochlorperazine may be found in breast milk it should not be used during lactation. Neonates exposed to antipsychotics (including prochlorperazine) 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.4.7 Effects on ability to drive and use machines Patients who drive or operate machinery should be warned of the possibility of drowsiness.4.8 Undesirable effects Undesirable effects are listed by MedDRA System Organ Classes. Assessment of undesirable effects is based on the following frequency groupings: Very common: ≥1/10 Common: ≥1/100 to <1/10 Uncommon: ≥1/1,000 to <1/100 Rare: ≥1/10,000 to <1/1,000 Very rare: <1/10,000 Not known: cannot be estimated from the available data \*\*Tabulated list of adverse reactions\*\* | | | | --- | --- | | \*\*System organ class\*\* | \*\*Undesirable effect and frequency\*\* | | Blood and lymphatic system disorders | \*Rare:\* Blood dyscrasia | | Immune system disorders | \*Not known:\* Hypersensitivity reactions such as rash and angioedema | | Endocrine disorders | \*Very rare:\* Hyperprolactinaemia which may result in gynaecomastia, galactorrhoea and amenorrhoea | | Metabolism and nutrition disorders | \*Not known:\* Hyponatraemia Syndrome of inappropriate antidiuretic hormone secretion Hyperglycaemia Glucose tolerance impaired | | Psychiatric disorders | \*Not known:\* Insomnia Agitation | | Nervous system disorders | \*Not known:\* Convulsion Drowsiness Dizziness Extrapyramidal reactions including acute dystonia, akathisia, parkinsonism and tardive dyskinesia | | Cardiac disorders | \*Not known:\* Arrythmia\\* QT prolongation\\* | | Vascular disorders | \*Not known:\* Hypotension (usually orthostatic) | | Gastrointestinal disorders | \*Not known:\* Dry mouth Irritation gum Mouth irritation Hypoaesthesia oral Paraesthesia oral Taste disorders | | Hepatobiliary disorders | \*Rare:\* Jaundice \*Not known:\* Cholestasis | | Skin and subcutaneous tissue disorders | \*Not known:\* Skin reaction Photosensitivity (see section 4.4) | | Pregnancy, puerperium and perinatal conditions | \*Not known:\* Drug withdrawal syndrome neonatal (see Section 4.6) | \\* See 'Description of selected adverse reactions' \*\*\*\*Description of selected adverse reactions\*\*\*\* Impotence, ejaculation disorder, priapism, and agranulocytosis (see section 4.4) are class effects associated with phenothiazines. Neuroleptic malignant syndrome may occur with any neuroleptic (see section 4.4). Cases of venous thromboembolism, including cases of pulmonary embolism and cases of deep vein thrombosis have been reported with antipsychotic drugs- Frequency unknown (see section 4.4). QT prolongation, cardiac arrhythmias, including ventricular arrhythmias which may result in ventricular fibrillation or cardiac arrest have been reported during neuroleptic phenothiazine therapy. Pre-existing cardiac disease, proarrhythmic conditions, hypokalaemia, hypomagnesemia, or concomitant administration with QT interval prolonging drugs may predispose. \*\*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.4.9 Overdose The signs and symptoms will be predominantly extrapyramidal and may be accompanied either by restlessness and agitation or central nervous depression. Hypotension may also occur. Treatment is essentially symptomatic and supportive. There is no specific antidote. Do not induce vomiting. Particular attention must be directed to maintaining a clear airway since this may be threatened by extrapyramidal muscle dystonias. Severe dystonic reactions usually respond to procyclidine or orphenadrine given i.m. or i.v. If convulsions occur they should be treated using i.v. diazepam. If hypotension is present, strict attention to ventilation and posturing of the patient will often secure the desired effect, but failing this, consideration should be given to volume expansion by i.v. fluids. If this is insufficient, positive inotropic agents such as dopamine may be tried, but peripheral vasoconstrictor agents are not generally recommended. Adrenaline should \*\*NOT\*\* be used. ## Pharmacological Properties 5.1 Pharmacodynamic properties Pharmacotherapeutic group: Phenothiazines with piperazine structure ATC code: N05AB Prochlorperazine is a member of the phenothiazine group of neuroleptics which, in doses lower than those used in psychiatry, is usually employed for its anti-emetic properties. The site of action is thought to be the chemoreceptor trigger zone.5.2 Pharmacokinetic properties The buccal tablets are placed in the buccal cavity where they form a gel from which the prochlorperazine is released and absorbed. The plasma levels achieved at steady-state on a dosage regimen of one buccal tablet twice daily are similar to those observed with the standard oral dosage of one 5 mg tablet taken three times daily. The elimination half-life of prochlorperazine in this formulation is 9.0 hours, similar to that observed with the oral formulation.5.3 Preclinical safety data No preclinical findings of relevance have been reported. ## Pharmaceutical Particulars 6.1 List of excipients Compressible sugar, povidone K30, xanthan gum, locust bean gum, talc, magnesium stearate and riboflavin sodium phosphate.6.2 Incompatibilities None.6.3 Shelf life Three years for blister packs. Two years for plastic tubs.6.4 Special precautions for storage Protect from light.6.5 Nature and contents of container 250 micron PVC/PVdC aluminium foil blister packs or plastic tubs. Pack size: Blister packs of 2, 8, 15, 30, 50, or 60 tablets. Plastic tubs of 250 tablets.6.6 Special precautions for disposal and other handling No special requirements.
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