SUMMARY OF PRODUCT CHARACTERISTICS

1    NAME OF THE MEDICINAL PRODUCT

Promazine Hydrochloride 25mg/5ml Oral Syrup

2    QUALITATIVE AND QUANTITATIVE    COMPOSITION

Promazine Hydrochloride 25mg/5ml

3    PHARMACEUTICAL FORM

Oral Syrup

4    CLINICAL PARTICULARS

4.1    Therapeutic indications

1.    As an adjunct to short-term management of moderate to severe psychomotor agitation

2.    Agitation and restlessness in the elderly

4.2    Posology and method of administration

Posology

For oral administration only.

Dosage varies with the individual and the purpose for which the drug is used, so the following dosages are only for general guidance with regard to possible effectiveness and good tolerance.

Initial dosages should be low, with increments at frequent, regular intervals until the desired response is obtained. Dosage intervals are usually six to eight hours, but in some patients the 24 hour requirement may be conveniently administered in a single bedtime dose.

The commencement and increase of dosage should be performed under close supervision.

Psychomotor Agitation

Adults: 100mg to 200mg, four times daily.

Elderly: Half the normal starting dose may be sufficient for a therapeutic response. Agitation and Restlessness

Elderly: 25mg initially, increasing, if necessary, up to 50mg, four times a day.

Children: Promazine is not recommended for children

4.3 Contraindications

Use in patients hypersensitive to the active ingredient or other phenothiazines.

Use in patients in coma or CNS depression Use in patients with bone marrow depression Use in patients with phaeochromocytoma Use during lactation

Do not use during pregnancy, especially during the first three months, unless there are compelling reasons.

4.4 Special warnings and precautions for use

1.    Acute withdrawal symptoms, including nausea, vomiting, sweating and insomnia have been described after abrupt cessation of antipsychotic drugs. Recurrence of psychotic symptoms may also occur, and the emergence of involuntary movement disorders (such as akathisia, dystonia and dyskinesia) has been reported. Therefore, gradual withdrawal is advisable.

2.    Phenothiazine should only be used with great caution in patients with a history of jaundice or with existent liver dysfunction, or blood dyscrasias, (perform blood counts if unexplained infection or fever occurs) coronary insufficiency or cardiac disease.

3.    Respiratory depression may occur in patients with severe respiratory disease.

4.    Promazine should be used with caution in patients with renal failure.

5.    Patients receiving phenothiazines over a prolonged period require regular and careful surveillance with particular attention to potential for inducing eye changes (corneal and lens opacities and purplish pigmentation of the skin, cornea, conjunctiva and retina), effects on haemopoiesis, liver dysfunction, myocardial conduction effects, particularly if other concurrently administered drugs also have potential effects on these systems.

6.    Use of phenothiazines at high (relative or absolute) doses may induce extrapyramidal side effects, dyskinesia, akathisia, dystonia. These are likely to be particularly severe in children. Caution should be exercised in patients with Parkinson’s disease. Anti-parkinson agents should not be prescribed routinely because of the risk of aggravating anticholinergic side effects of Promazine, of precipitating toxic-confusional states or of impairing its therapeutic efficacy. They should be given only as required.

7.    Prolonged administration of phenothiazines may result in persistent or tardive dyskinesias particularly in the elderly. The risk of tardive dyskinesia and the likelihood of irreversibility are believed to increase as the duration of therapy and total cumulative dose increase. Neuroleptic therapy should be withdrawn if dyskinesia develops.

8.    Care should be exercised if Promazine is used for the treatment of patients with cerebral arteriosclerosis, coronary heart disease or other conditions in which a fall in blood pressure might be undesirable.

9.    Caution should be observed with patients suffering from epilepsy or conditions predisposing to epilepsy.

10.    Personal or family history of narrow angle glaucoma.

11.    Phenothiazines may impair body temperature regulation. Caution should be observed in very hot or very cold weather.

12.    Hypothyroidism.

13.    Myasthenia gravis.

14.    Phaeochromocytoma.

15.    Prostatic hypertrophy.

16.    Antipsychotic drugs may increase prolactin secretion.

17.    An approximately 3-fold increased risk of cerebrovascular adverse events have been seen in randomised placebo controlled clinical trials in the dementia population with some atypical antipsychotics. The mechanism for this increased risk is not known. Promazine should be used with caution in patients with risk factors for stroke.

18.    As with other drugs belonging to the therapeutic class of antipsychotics, promazine may cause QT prolongation. Persistently prolonged QT intervals may increase the risk of malignant arrhythmias. Therefore, promazine should be used with caution in susceptible individuals (with hypoklaemia, hypomagnesia or genetic predisposition) and in patients with a history of cardiovascular disorders, e.g. QT prolongation, significant bradycardia (<50 beats per minute), a recent acute myocardial infarction, uncompensated heart failure, or cardiac arrhythmia. Concomitant treatment with other antipsychotics should be avoided (See section 4.5).

19.    Concomitant use of promazine with other neuroleptics should be avoided.

20.    Photosensitisation may occur, particularly at higher doses. Patients should be advised to avoid direct sunlight.

21.    The elderly are particularly susceptible to the side effects of promazine, particularly hypotension, sedation and temperature regulation effects.

22.    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 Promazine and preventive measures undertaken.

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.

Promazine is not licensed for the treatment of dementia-related behavioural disturbances.

Excipients in the Formulation

This product contains hydroxybenzoate esters. These are known to cause urticaria, delayed type reactions such as contact dermatitis and rarely an immediate reaction with urticaria and bronchospasm.

Promazine Syrup contains liquid glucose. Patients with rare glucose-galactose malabsorption should not take this medicine.

Promazine Syrup contains sucrose. Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltase insufficiency should not take this medicine.

4.5 Interaction with other medicinal products and other forms of interaction

The concomitant administration of this product with other medication such as central nervous system depressants (including alcohol and anaesthetics) or antihypertensives, opioids, anticholinergic or dopaminergic drugs may result in accentuation of their effects, while potentiation of action may also occur with monoamine oxidase inhibitors, antidepressants and analgesics. Promazine may impair the effects of anticonvulsants. Promazine may affect the control of diabetes and possibly antagonises the hypoglycaemic effect of sulfonylureas. Undesirable anticholinergic effects can be enhanced by anti-parkinson or other anticholinergic drugs.

The concomitant administration of this product with myelosuppressive drugs (carbamazepine, co-trimoxazole, chloramphenicol, sulphonamides, pyralizone analgesics (e.g. azapropazone), penicillamine and cytotoxics) increases the risk of toxicity.

Lithium administration will result in an increased risk of extrapyramidal effects and the possibility of neurotoxicity.

Coadministration of phenothiazines with metoclopramide or tetrabenazine increases the risk of extrapyramidal effects.

An increase in plasma concentration of antipsychotic drugs may occur if taken with ritonavir.

There is an increased risk of CNS toxicity if sibutramine is taken concomitantly with phenothiazines.

There is an increased risk of convulsions when promazine is coadministered with tramadol

Antipsychotic drugs antagonize the pressor effects of sympathomimetics.

The effects of antipsychotic drugs may be enhanced by cimetidene and reduced by memantine.

Antacids and kaolin may reduce absorption of phenothiazines.

Caution should be used when using antipsychotics with reboxetine.

Sotalol administration will result in an increased risk of ventricular arrhythmia.

Concomitant use of promazine with drugs known to prolong the QT interval may increase the risk of ventricular arrhythmias, including torsade de pointes. Therefore concomitant use of these products is not recommended. Examples include certain antiarrhythmics, such as those of Class 1A (such as quinidine, disopyramide and procainamide) and Class III (such as amiodarone, sotalol and dofetilide), certain antimicrobials (sparfloxacin, moxifloxacin, erythromycin IV), tricyclic antidepressants (such as amitriptyline), certain tetracyclic antidepressants (such as maprotiline), other neuroleptics (e.g. phenothiazines, pimozide, sertindole and haloperidol), certain antihistamines (such as terfenadine), cisapride, bretylium and certain antimalarials such as quinine and mefloquine. This list is not comprehensive.

Concurrent use of drugs causing electrolyte imbalance is not recommended. Diuretics, in particular those causing hypokalemia, should be avoided but, if necessary, potassium-sparing diuretics are preferred.

4.6 Fertility, pregnancy and lactation

Do not use during pregnancy, especially during the first three months, unless there are compelling reasons. There is insufficient evidence of the safety of Promazine in human pregnancy nor is there evidence from animal studies that it is free from hazard.

Promazine should not be used during lactation.

Neonates exposed to antipsychotics (including Promazine) 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

Phenothiazines may impair alertness and induce drowsiness especially at the start of treatment. Alcohol and many other drugs (see section 4.5) may enhance these effects and impair the ability to drive.

Persons taking these drugs should not drive or operate machinery unless the drug has been shown not to interfere with physical or mental ability.

4.8 Undesirable effects

Promazine is a member of the phenothiazine group of drugs and the size effects associated with that group have been noted.

System Organ Class
Blood and lymphatic system disorders	Sensitivity reactions including agranulocytosis, leucopenia, haemolytic anaemia.
Psychiatric disorders	Apathy, confusional state. Some individuals may be susceptible to the drug in low dosage and show paradoxical effects of excitement, agitation or insomnia and other minor side effects. Withdrawal symptoms, including nausea, vomiting, sweating, insomnia, recurrence of psychotic symptoms and involuntary movement disorders have been noted (see Section 4.4).
Nervous system disorders	Drowsiness, dizziness, headache, sedation, epileptic fits, extrapyramidal symptoms (dystonia, tremor, tardive dyskinesia and akathisia), neuroleptic malignant syndrome (hyperthermia, rigidity, autonomic dysfunction, altered consciousness) may occur with any neuroleptic.
Eye disorders	Blurred vision, precipitation of glaucoma, corneal and lens opacities and purplish pigmentation of the skin, cornea, conjunctiva and retina.
Cardiac disorders	Tachycardia, cardiovascular effects include hypotension. Phenothiazines can produce ECG changes with

	prolongation of QT interval and T-wave changes, ventricular arrhythmias (VF, VT (rare)), sudden unexplained death, cardiac arrest and Torsades de pointes have been reported.
Respiratory, thoracic and mediastinal disorders	Nasal stuffiness
Gastrointestinal disorders	Gastrointestinal disturbances, dry mouth, constipation.
Hepatobiliary disorders	Transient abnormalities of liver function tests may occur without jaundice. Rarely - obstructive jaundice associated with stasis in biliary canaliculi. Treatment should then be withdrawn and not given again.
Skin and subcutaneous tissue disorder	Sensitivity reactions including allergic skin reactions, rashes, photosensitisation and contact sensitization.
Renal and urinary disorders	Urinary hesitancy or retention when due to enlarged prostate.
Reproductive system and breast disorders	Menstrual disturbances, galactorrhoea, gynaecomastia, impotence.
General disorders and administration site conditions	Hypothermia, hyperpyrexia.
Pregnancy, puerperium and perinatal conditions:	Not known: Drug withdrawal syndrome neonatal (see 4.6).
Investigations	Weight gain

The elderly are particularly susceptible to side effects of Promazine, especially to the sedative, hypotensive and temperature regulation effects. This may be dose related.

Cases of venous thromboembolism, including cases of pulmonary embolism and cases of deep vein thrombosis have been reported with antipsychotic drugs -Frequency unknown

4.9 Overdose

Ingestion of large amounts of Promazine is followed by deep sleep, with or without a pronounced fall in blood pressure and without particular change in respiration rate, other than the slowing attendant upon sedation. Occasionally an initial period of excitement may precede coma, followed by grand mal seizures.

In the absence of any specific antidote, treatment should be based on ordinary therapeutic principles with special emphasis on the following measures:

a.    Gastric lavage;

b.    Treat convulsions if present;

c.    Correction of acute hypotension if necessary;

d.    Counteraction of the effects of an excess of Promazine on the central nervous system;

e.    Control and natural recovery of hypothermia.

5.1 Pharmacodynamic properties

Promazine has a wide range of activity arising from its depressant actions on the central nervous system and its alpha-adrenergic blocking and weaker anticholinergic activities. It is a dopamine inhibitor; it inhibits prolactin release-inhibitory factor, considered to be dopamine, thus stimulating the release of prolactin. The turnover of dopamine in the brain is also increased.

5.2 Pharmacokinetic properties

Promazine is readily absorbed from the gastro-intestinal tract but is subject to considerable first-pass metabolism in the gut wall. It is also extensively metabolised in the liver and is excreted in the urine and faeces in the form of numerous active and inactive metabolites; there is evidence of enterohepatic recycling. Owing to the first-pass effect, plasma concentrations following oral administration are much lower than those following intramuscular administration.

Moreover, there is very wide intersubject variation in plasma concentrations of Promazine; no simple correlation has been found between plasma concentrations of Promazine and its metabolites, and their therapeutic effect. Paths of metabolism of Promazine include hydroxylation and conjugation with glucuronic acid, N-oxidation, oxidation of a sulphur atom, and dealkylation. Its duration of therapeutic effect can range from a few days to several weeks or possibly longer.

Promazine is very extensively bound to plasma proteins. It is widely distributed in the body and crosses the blood-brain barrier to achieve higher concentrations in the brain than in the plasma. Promazine and its metabolites also cross the placental barrier and are excreted in milk.

5.3 Preclinical safety data

None stated

6    PHARMACEUTICAL PARTICULARS

6.1    List of excipients

Propylene glycol (E1520), methyl hydroxybenzoate (E218), ethyl hydroxybenzoate (E214) and propyl hydroxybenzoate (E216), sucrose, liquid glucose, ascorbic acid (E300), green lemon flavour 545489E and purified water.

6.2 Incompatibilities

None known 24 months

6.4 Special Precautions for Storage

Store below 25°C. Protect from light.

6.5    Nature and contents of container

Bottle: Amber (type III) glass bottle Capacity: 150ml

Closure: HDPE, EPE wadded, tamper evident, child resistant closure.

6.6    Special precautions for disposal

Dispense in amber glass bottles. If a dose of under 5ml is required, the oral syrup should be administered using an oral dosing device.

7    MARKETING AUTHORISATION    HOLDER

Rosemont Pharmaceuticals Limited

Rosemont House

Yorkdale Industrial Park

Braithwaite Street

Leeds

LS11 9XE

8    MARKETING AUTHORISATION    NUMBER(S)

PL 00427/0054

9    DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

05/02/1982 / 05/04/2002

10 DATE OF REVISION OF THE TEXT

04/05/2016