Monday, October 17, 2016

Haloperidol Injection BP 5mg / ml





1. Name Of The Medicinal Product



Haloperidol Injection BP 5mg/ml, 1ml & 2ml.


2. Qualitative And Quantitative Composition



Each ml of solution contains Haloperidol BP 5mg.



3. Pharmaceutical Form



Sterile solution for injection.



4. Clinical Particulars



4.1 Therapeutic Indications



Haloperidol is a butyrophenone neuroleptic drug with a wide range of actions. It is indicated for the rapid control of the symptoms of hostility, aggression, hyperactivity, disruptive and violent behaviour, confusion, emotional withdrawal, hallucinations and delusions associated with acute and chronic schizophrenia, mania, and hypomania, and organic brain syndrome. Haloperidol is also indicated for the treatment of nausea and vomiting.



4.2 Posology And Method Of Administration



Haloperidol Injection is recommended for intramuscular administration only.



Adults: As with all neuroleptic agents, it is essential to titrate the dose of haloperidol to individual patient requirements, and this should be done as rapidly as is practicable to achieve optimum therapeutic benefit. In determining the initial dose, account should be taken of the patient's age, severity of symptoms and previous response to other neuroleptic drugs. The dosage should be increased progressively until maximum control of symptoms is achieved. Thereafter, the dosage may be reduced, gradually, to the lowest effective maintenance dosage.



Elderly or debilitated patients or those with previous adverse reactions to neuroleptic agents may require less haloperidol, and half the normal starting dose may be sufficient for therapeutic purpose. In such patients, the optimum response is usually achieved with more gradual titration and at lower dose levels.



A lower dose may be advisable for prompt control of acutely agitated patients with moderate symptoms, initial doses of 2 to 10mg intramuscularly, may be used. Depending on the response of the patients, subsequent doses may be given every 4-8 hours up to a maximum of 18mg/day. Oral treatment should succeed intramuscular administration as soon as possible. Within this context, bioavailability from the oral route is about 60% of that from the IM route and readjustment of dose may be required.



Children: Haloperidol injection is not recommended for use in children.



4.3 Contraindications



Known hypersensitivity to haloperidol, CNS depression, Parkinson's disease, and basal ganglia lesions.



Haloperidol should not be administered to patients in coma.



In common with other neuroleptics, haloperidol has the potential to cause rare prolongation of the QT interval. Use of haloperidol is therefore contra-indicated in patients with clinically significant cardiac disorders (e.g. recent acute myocardial infarction, uncompensated heart failure, arrhythmias treated with class IA and III anti-arrhythmic medicinal products), QTc interval prolongation, history of ventricular arrhythmia or Torsades de pointes, clinically significant bradycardia, second or third degree heart block and uncorrected hypokalaemia.



Haloperidol should not be used concomitantly with other QT prolonging drugs (see section 4.5, Interaction with other medicinal products and other forms of interaction).



4.4 Special Warnings And Precautions For Use



Cases of sudden death have been reported in psychiatric patients receiving antipsychotic drugs, including haloperidol.



Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death.



Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7 times the risk of death in placebo-treated patients. Over the course of a typical 10 week controlled trial, the rate of death in drug-treated patients was about 4.5%, compared to a rate of about 2.6% in the placebo group. Although the causes of death were varied, most of the deaths appeared to be either cardiovascular (e.g., heart failure, sudden death) or infectious (e.g., pneumonia) in nature.



Observational studies suggest that, similar to atypical antipsychotic drugs, treatment with conventional antipsychotic drugs may increase mortality. The extent to which the findings of increased mortality in observational studies may be attributed to the antipsychotic drug as opposed to some characteristic(s) of the patients is not clear.



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.



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



Cardiovascular effects



Very rare reports of QT prolongation and/or ventricular arrhythmias, in addition to rare reports of sudden death, have been reported with haloperidol. They may occur more frequently with high doses and in predisposed patients.



The risk-benefit of haloperidol treatment should be fully assessed before treatment is commenced and patients with risk factors for ventricular arrhythmias such as cardiac disease; family history of sudden death and/or QT prolongation; uncorrected electrolyte disturbances; subarachnoid haemorrhage; starvation; alcohol abuse should be monitored carefully (ECGs and potassium levels), particularly during the initial phase of treatment, to obtain steady plasma levels.



The risk of QT prolongation and/or ventricular arrhythmias may be increased with higher doses (see Sections 4.8 and 4.9) or with parenteral use, particularly intravenous administration. ECG monitoring should be performed for QT interval prolongation and for serious cardiac dysrhythmias if Haloperidol is administered intravenously.



Haloperidol should be used with caution in patients known to be slow metabolisers of CYP2D6, and during use of cytochrome P450 inhibitors. Concomitant use of neuroleptics should be avoided (See Section 4.5).



Baseline ECG is recommended prior to treatment in all patients, especially in the elderly and patients with a positive personal or family history of cardiac disease or abnormal findings on cardiac clinical examination. During therapy, the need for ECG monitoring (e.g. at dose escalation) should be assessed on an individual basis. Whilst on therapy, the dose should be reduced if QT is prolonged, and haloperidol should be discontinued if the QTc exceeds 500 ms.



Periodic electrolyte monitoring is recommended, especially for patients taking diuretics, or during intercurrent illness.



An approximately 3-fold increase 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. An increased risk cannot be excluded for other antipsychotics or other patient populations. Haloperidol should be used with caution in patients with risk factors for stroke.



Neuroleptic malignant syndrome



In common with other antipsychotic drugs, Haloperidol has been associated with neuroleptic malignant syndrome: a rare idiosyncratic response characterised by hyperthermia, generalised muscle rigidity, autonomic instability, altered consciousness. Hyperthermia is often an early sign of this syndrome. Antipsychotic treatment should be withdrawn immediately and appropriate supportive therapy and careful monitoring instituted.



Tardive dyskinesia



As with all antipsychotic agents, tardive dyskinesia may appear in some patients on long-term therapy or after drug discontinuation. The syndrome is mainly characterised by rhythmic involuntary movements of the tongue, face, mouth or jaw. The manifestations may be permanent in some patients. The syndrome may be masked when treatment is reinstituted, when the dosage is increased or when a switch is made to a different antipsychotic drug. Treatment should be discontinued as soon as possible.



Extrapyramidal symptoms



In common with all neuroleptics, extrapyramidal symptoms may occur, e.g. tremor, rigidity, hypersalivation, bradykinesia, akathisia, acute dystonia.



Anti-parkinson drugs of the anticholinergic type may be prescribed as required, but should not be prescribed routinely as a preventive measure. If concomitant anti-parkinson medication is required, it may have to be continued after stopping Haloperidol if its excretion is faster than that of Haloperidol in order to avoid the development or aggravation of extrapyramidal symptoms. The physician should keep in mind the possible increase in intraocular pressure when anticholinergic drugs, including anti-parkinson agents, are administered concomitantly with Haloperidol.



Seizures/Convulsions



It has been reported that seizures can be triggered by Haloperidol. Caution is advised in patients suffering from epilepsy and in conditions predisposing to convulsions (e.g., alcohol withdrawal and brain damage).



Hepatobiliary concerns



As Haloperidol is metabolised by the liver, caution is advised in patients with liver disease. Isolated cases of liver function abnormalities or hepatitis, most often cholestatic, have been reported.



Endocrine system concerns



Thyroxin may facilitate Haloperidol toxicity. Antipsychotic therapy in patients with hyperthyroidism should be used only with great caution and must always be accompanied by therapy to achieve a euthyroid state.



Hormonal effects of antipsychotic neuroleptic drugs include hyperprolactinaemia, which may cause galactorrhoea, gynaecomastia and oligo- or amenorrhoea. Very rare cases of hypoglycaemia and of Syndrome of Inappropriate ADH Secretion have been reported.



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 Haloperidol and preventive measures undertaken.



Additional considerations



In schizophrenia, the response to antipsychotic drug treatment may be delayed. If drugs are withdrawn, recurrence of symptoms may not become apparent for several weeks or months.



Acute withdrawal symptoms including nausea, vomiting and insomnia have been very rarely described after abrupt cessation of high doses of antipsychotic drugs. Relapse may also occur and gradual withdrawal is advisable.



As with all antipsychotic agents, haloperidol should not be used alone where depression is predominant. It may be combined with antidepressants to treat those conditions in which depression and psychosis coexist.



Caution is advised in patients with renal failure and pheochromocytoma.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



Concomitant use of haloperidol 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 (see section 4.3-Contraindications).



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 and sertindole), certain antihistamines (such as terfenadine), cisapride, bretylium and certain anti-malarials such as quinine and mefloquine. This list is not comprehensive.



Concurrent use of drugs causing electrolyte imbalance may increase the risk of ventricular arrhythmias and is not recommended (see section 4.4-Special Warnings and Precautions for Use). Diuretics, in particular those causing hypokalaemia, should be avoided but, if necessary, potassium-sparing diuretics are preferred.



Haloperidol is metabolised by several routes, including glucuronidation and the cytochrome P450 enzyme system (particularly CYP 3A4 or CYP 2D6). Inhibition of these routes of metabolism by another drug or a decrease in CYP 2D6 enzyme activity may result in increased haloperidol concentrations and an increased risk of adverse events, including QT-prolongation. In pharmacokinetic studies, mild to moderately increased haloperidol concentrations have been reported when haloperidol was given concomitantly with drugs characterised as substrates or inhibitors of CYP 3A4 or CYP 2D6 isozymes, such as, itraconazole, buspirone, venlafaxine, alprazolam, fluvoxamine, quinidine, fluoxetine, sertraline, chlorpromazine, and promethazine. A decrease in CYP2D6 enzyme activity may result in increased haloperidol concentrations. Increases in QTc and extrapyramidal symptoms have been observed when haloperidol was given with a combination of the metabolic inhibitors ketoconazole (400 mg/day) and paroxetine (20 mg/day). It may be necessary to reduce the haloperidol dosage.



Effect of Other Drugs on Haloperidol



When prolonged treatment with enzyme-inducing drugs such as carbamazepine, phenobarbital, rifampicin is added to Haloperidol therapy, this results in a significant reduction of haloperidol plasma levels. Therefore, during combination treatment, the Haloperidol dose should be adjusted, when necessary. After stopping such drugs, it may be necessary to reduce the dosage of Haloperidol.



Sodium valproate, a drug known to inhibit glucuronidation, does not affect haloperidol plasma concentrations.



Effect of Haloperidol on Other Drugs



In common with all neuroleptics, Haloperidol can increase the central nervous system depression produced by other CNS-depressant drugs, including alcohol, hypnotics, sedatives or strong analgesics.



An enhanced CNS effect, when combined with methyldopa, has also been reported.



Haloperidol may antagonise the action of adrenaline and other sympathomimetic agents and reverse the blood-pressure-lowering effects of adrenergic-blocking agents such as guanethidine.



Haloperidol may impair the antiparkinson effects of levodopa.



Haloperidol is an inhibitor of CYP 2D6. Haloperidol inhibits the metabolism of tricyclic antidepressants, thereby increasing plasma levels of these drugs.



Other Forms of Interaction



In rare cases, an encephalopathy-like syndrome has been reported in combination with lithium and haloperidol. It remains controversial whether these cases represent a distinct clinical entity or whether they are in fact cases of NMS and/or lithium toxicity. Signs of encephalopathy-like syndrome include confusion, disorientation, headache, disturbances of balance and drowsiness. One report showing symptomless EEG abnormalities on the combination has suggested that EEG monitoring might be advisable. When lithium and haloperidol therapy are used concomitantly, haloperidol should be given in the lowest effective dose and lithium levels should be monitored and kept below 1 mmol/l. If symptoms of encephalopathy-like syndrome occur, therapy should be stopped immediately.



Antagonism of the effect of the anticoagulant phenindione has been reported.



The dosage of anticonvulsants may need to be increased to take account of the lowered seizure threshold.



4.6 Pregnancy And Lactation



The safety of haloperidol in pregnancy has not been established. There is some evidence of harmful effects in some but not all animal studies. There have been a number of reports of birth defects following foetal exposure to haloperidol for which a causal role for haloperidol cannot be excluded. Reversible extra-pyramidal symptoms have been observed in neonates exposed to haloperidol in utero during the last trimester of pregnancy.



Haloperidol should be used during pregnancy only if the anticipated benefit outweighs the risk and the administered dose and duration of treatment should be as low and as short as possible.



Haloperidol is excreted in breast milk. There have been isolated cases of extrapyramidal symptoms in breast-fed children. If the use of haloperidol is essential, the benefits of breast-feeding should be balanced against its potential risks.



4.7 Effects On Ability To Drive And Use Machines



Haloperidol may cause drowsiness, blurred vision, and impair alertness. Patients should be advised not to undertake activities such as to drive or operate machinery during treatment.



4.8 Undesirable Effects



The data provided below covers all haloperidol formulations including the Haloperidol Decanoate formulations.



Very common (








































































































































System Organ Class




Adverse Drug Reactions


    


 




Frequency Category


    


 




Very Common



(




Common



(




Uncommon



(




Rare



(




Not Known




Blood and lymphatic System Disorders




 



 



 




 



 



 




Leukopenia




 



 



 




Agranulocytosis; Neutropenia; Pancytopenia; Thrombocytopenia




Immune System Disorders




 



 



 




 



 



 




Hypersensitivity




 



 



 




Anaphylactic reaction




Endocrine Disorders




 



 



 




 



 



 




 



 



 




Hyperprolactinaemia




Inappropriate antidiuretic hormone secretion




Metabolic and Nutritional Disorders




 



 



 




 



 



 




 



 



 




 



 



 




Hypoglycaemia




Psychiatric Disorders




Agitation; Insomnia




Depression; Psychotic disorder




Confusional state; Libido Decreased; Loss of libido; Restlessness




 



 



 




 



 



 




Nervous System Disorders




Extrapyramidal disorder; Hyperkinesia; Headache




Tardive dyskinesia; Oculogyric Crisis; Dystonia; Dyskinesia; Akathisia; Bradykinesia; Hypokinesia; Hypertonia; Somnolence; Masked Facies, Tremor; Dizziness




Convulsion; Parkinsonism; Akinesia; Cogwheel rigidity; Sedation; Muscle Contractions Involuntary




Motor dysfunction; Neuroleptic malignant syndrome; Nystagmus;




 



 



 




Eye Disorders




 



 



 




Visual disturbance;




Vision blurred




 



 



 




 



 



 




Cardiac Disorders




 



 



 




 



 



 




Tachycardia




 



 



 




Ventricular Fibrillation; Torsade de pointes; Ventricular Tachycardia; Extrasystoles




Vascular Disorders




 



 



 




Orthostatic Hypotension; Hypotension




 



 



 




 



 



 




 



 



 




Respiratory, thoracic and mediastinal Disorders




 



 



 




 



 



 




Dyspnoea




Bronchospasm




Laryngeal Oedema; Laryngospasm




Gastrointestinal Disorders




 



 



 




Constipation; Dry mouth; Salivary hypersecretion;Nausea; Vomiting




 



 



 




 



 



 




 



 



 




Hepatobiliary Disorders




 



 



 




Liver function test abnormal




Hepatitis; Jaundice




 



 



 




Acute Hepatic Failure; Cholestasis




Skin and subcutaneous tissue disorders




 



 



 




Rash




Photosensitivity Reaction; Urticaria; Pruritus; Hyperhidrosis




 



 



 




Leukocytoclastic Vasculitis; Dermatitis Exfoliative




Musculoskeletal and Connective Tissue Disorders




 



 



 




 



 



 




Torticollis; Muscle rigidity; Muscle Spasms; Musculoskeletal stiffness




Trismus; Muscle Twitching




 



 



 




Renal and Urinary Disorders




 



 



 




Urinary retention




 



 



 




 



 



 




 



 



 




Reproductive System and Breast Disorders




 



 



 




Erectile dysfunction




Amenorrhoea; Dysmenorrhoea; Galactorrhoea; Breast Discomfort; Breast Pain;




Menorrhagia; Menstrual Disorder; Sexual Dysfunction




Gynaecomastia, Priapism




General Disorders and Administration Site Conditions




 



 



 




Injection Site Reaction




Gait disturbance; Hyperthermia; Oedema




 



 



 




Sudden Death; Face Oedema; Hypothermia




Investigations




 



 



 




Weight increased; Weight decreased




 



 



 




Electrocardiogram QT prolonged




 



 



 




 




 




 




 




 




 



Additional Information



Cardiac effects such as QT-interval prolongation, torsade de pointes, ventricular arrhythmias, including ventricular fibrillation and ventricular tachycardia), and cardiac arrest have been reported. These effects may occur more frequently with high doses, and in predisposed patients.



Toxic epidermal necrolysis and Stevens-Johnson syndrome have been reported in patients taking haloperidol. The true incidence of these reports is not known.



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



Symptoms: In general, the manifestations of haloperidol overdosage are an extension of its pharmacological actions, the most prominent of which would be severe extrapyramidal symptoms, hypotension and psychic indifference with a transition to sleep. The risk of ventricular arrhythmias possibly associated with QT-prolongation should be considered. The patient may appear comatose with respiratory depression and hypotension which could be sever enough to produce a shock-like state. Paradoxically hypertension rather than hypotension may occur. Convulsions may also occur.



Treatment:



There is no specific antidote to haloperidol, and treatment of overdose is symptomatic and supportive. A patent airway should be established and maintained with mechanically assisted ventilation if necessary. In view of isolated reports of arrhythmia, ECG monitoring is strongly advised. Hypotension and circulatory collapse should be treated by plasma volume expansion and other appropriate measures. Adrenaline should not be used. The patient should be monitored carefully for 24 hours or longer. Body temperature and adequate fluid intake should be maintained.



Severe extrapyramidal manifestations should be treated with appropriate antiparkinsonian medications.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Haloperidol is a member of the butyrophenone class of neuroleptic drugs. The antipsychotic, antianxiety and antiemetic effects of haloperidol have been well demonstrated. Although the precise mechanism of action has not been elucidated, antagonism of dopamine-mediated synaptic neurotransmission appears to be an important action of haloperidol and may be the primary action through which the antipsychotic and extrapyramidal neurologic effects are mediated.



Within the autonomic nervous system, haloperidol displays weak anticholinergic activities. Orthostatic hypotension that is mediated by a combination of central actions and peripheral alpha-adrenergic blockade, occurs less frequently during treatment with haloperidol in comparison with other antipsychotic therapy. Haloperidol binds to opiate receptors.



5.2 Pharmacokinetic Properties



Haloperidol is well absorbed from the intramuscular sites. Variable bioavailability is likely due to the extent of first-pass hepatic metabolism. Metabolism is by oxidative dealkylation. The elimination half-life is approximately 20hours. Haloperidol is extensively bound to plasma proteins, is widely distributed throughout the body and crosses the blood-brain barrier. Metabolites of haloperidol appear to be inactive and excretion occurs via urine and faeces.



5.3 Preclinical Safety Data



No further relevant information other than that which is included in other sections of the Summary of Product Characteristics.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Lactic Acid



Sodium Hydroxide (as 10% w/v solution)



Water for injections



6.2 Incompatibilities



Haloperidol Injection should not be mixed with other products unless their compatibility is known.



6.3 Shelf Life



3 years (36 months)



If only part of the contents of an ampoule is used, the remaining solution should be discarded.



6.4 Special Precautions For Storage



Store in the original carton in order to protect from light



Do not store above 25°C.



6.5 Nature And Contents Of Container



1ml & 2 ml clear One Point Cut (OPC) glass ampoules, glass type 1 Ph. Eur. borosilicate glass packed in cardboard cartons to contain 10x1ml ampoules and 10x2ml ampoules.



6.6 Special Precautions For Disposal And Other Handling



Not applicable.



7. Marketing Authorisation Holder



Antigen International Ltd



Roscrea



Co.Tipperary



Ireland



8. Marketing Authorisation Number(S)



PL 02848/0127



9. Date Of First Authorisation/Renewal Of The Authorisation



Date of first authorisation: 27/9/89



Date of last renewal: 18/7/2008



10. Date Of Revision Of The Text



28/11/2011




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