Dalmane 15mg Capsules
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Dalmane 15mg Capsules
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
ICN
Capsules with an opaque grey cap and opaque yellow body with 15 printed in red on both cap and body, containing 16,4 mg flurazepam monohydrochloride (equivalent to 15 mg flurazepam).
Each capsule contains 114.6 mg lactose.
For the full list of excipients, see section 6.1
3. PHARMACEUTICAL FORM
Dalmane capsules 15 mg.
4. CLINICAL PARTICULARS
4.1. Therapeutic indications
Short-term treatment of insomnia when it is severe, disabling or subjecting the individual to extreme distress. Dalmane is helpful in overcoming difficulties in getting to sleep and also in the problem of frequent nocturnal awakenings. Its properties make it particularly indicated where the total duration of sleep is less than adequate.
An underlying cause for insomnia should be sought before deciding upon the use of benzodiazepines for symptomatic relief.
Beuzodiazepines are not recommended for the primary treatment of psychotic illness.
4.2. Posology and method of administration
Adults
The dosage of Dalmane should be determined on an individual basis taking into account the severity of the insomnia and the patient’s response to treatment. Dosage is important in determining the duration of effect and the occurrence of residual effects. For most patients the optimum dose if 15 mg -this will ensure a full night’s sleep with minimal residual effects on wakening. Patients with severe insomnia may require 30 mg but residual effects on awakening, associated with an anxiolytic effect, are more frequent at this dose.
Elderly
Elderly or debilitated patients. The elderly or patients with impaired renal and/or hepatic function will be particularly susceptible to the adverse effects of Dalmane. The initial dose should not exceed 15 mg. If organic brain changes are present, the dosage of Dalmane should not exceed 15 mg in these patients.
In patients with chronic pulmonary insufficiency and in patients which chronic renal or hepatic disease, dosage may need to be reduced.
Children
Dalmane is contra-indicated for use in children.
Treatment should, if possible, be on an intermittent basis.
Treatment should be as short as possible and should be started with the lowest recommended dose. The maximum dose should not be exceeded. Generally the duration of treatment varies from a few days to two weeks with a maximum of four weeks, including the tapering off process. Patients who have taken benzodiazepines for a prolonged time may require a longer period during which doses are reduced. Specialist help may be appropriate. Little is known regarding the efficacy or safety of benzodiazepines in long-term use.
In certain cases, extension beyond the maximum treatment period may be necessary; if so, it should not take place without re-evaluation of the patient’s status. Long-term chronic use is not recommended.
The product should be taken just before going to bed.
Dalmane capsules are for oral administration.
4.3 Contraindications
Dalmane is contraindicated in:
• patients with known hypersensitivity to flurazepam, other benzodiazepines or to any of the excipients listed in section 6.1
• myasthenia gravis
• severe pulmonary insufficiency
• respiratory depression
• phobic or obsessional states
• chronic psychosis
• sleep apnoea syndrome
• severe hepatic insufficiency
• use in children.
4.4. Special warnings and precautions for use
In patients with chronic pulmonary insufficiency, and in patients with chronic renal or hepatic disease, dosage may need to be reduced.
Dalmane should not be used alone to treat depression or anxiety associated with depression, since suicide may be precipitated in such patients.
In cases of loss or bereavement, psychological adjustment may be inhibited by benzodiazepines.
If the patient is awoken during the period of maximum drug activity, recall may be impaired.
Use of benzodiazepines may lead to the development of physical and psychological dependence. The dependence potential of the benzodiazepines is low, particularly when limited to short-term use, but this increases when high doses are used, especially when given over long periods. This is particularly so in patients with a history of alcoholism or drug abuse or in patients with marked personality disorders. Regular monitoring in such patients is essential, routine repeat prescriptions should be avoided and treatment should be withdrawn gradually. Symptoms such as depression, nervousness, extreme anxiety, tension, restlessness, confusion, mood changes, rebound insomnia, irritability, sweating, diarrhoea, headaches and muscle pain have been reported following abrupt cessation of treatment in patients receiving even normal therapeutic doses for short periods of time.
In severe cases the following symptoms may occur: derealisation, depersonalisation, hyperacusis, numbness and tingling of the extremities, hypersensitivity to light, noise and physical contact and hallucinations or epileptic seizures. In rare instances, withdrawal following excessive dosages may produce confusional states, psychotic manifestations and convulsions. Abuse of the benzodiazepines has been reported.
Some loss of efficacy to the hypnotic effects of short-acting benzodiazepines may develop after repeated use for a few weeks.
Abnormal psychological reactions to benzodiazepines have been reported.
Rare behavioural effects include paradoxical aggressive outbursts, excitement, confusion, restlessness, agitation, irritability, delusion, rages, nightmares, hallucinations, psychoses, inappropriate behaviour and the uncovering of depression with suicidal tendencies. Extreme caution should therefore be used in prescribing benzodiazepines to patients with personality disorders. If any of these reactions occur, use of the drug should be discontinued. These reactions may be quite severe and are more likely to occur in children and the elderly.
Benzodiazepines may induce anterograde amnesia. The condition usually occurs 1-2 hours after ingesting the product and may last up to several hours. Therefore, to reduce the risk, patients should ensure that they will be able to have an uninterrupted sleep of 7 to 8 hours.
4.5 Interaction with other medicinal products and other forms of interaction
Enhancement of the central depressive effect may occur if benzodiazepines are combined with centrally-acting drugs such as neuroleptics, tranquilisers, antidepressants, hypnotics, analgesics, enhancement of the euphoria may also occur leading to an increase in psychological dependence. The elderly require special supervision.
When Dalmane is used in conjunction with anti-epileptic drugs, side-effects and toxicity may be more evident, particularly with hydantoins or barbiturates or combinations including them. This requires extra care in adjusting dosage in the initial stages of treatment.
Known inhibitors of hepatic enzymes, e.g. cimetidine, have been shown to reduce the clearance of benzodiazepines and may potentiate their action and known inducers of hepatic enzymes, eg rifampicin, may increase the clearance of benzodiazepines.
Concomitant intake with alcohol should be avoided. The sedative effect may be enhanced when the product is used in combination with alcohol. This adversely affects the ability to drive or use machines.
4.6 Fertility, pregnancy and lactation
Pregnancy
There is no evidence as to drug safety in human pregnancy, nor is there evidence from animal work that it is free from hazard. Do not use during pregnancy, especially during the first and last trimesters, unless there are compelling reasons.
If the product is prescribed to a woman of childbearing potential, she should be warned to contact her physician regarding discontinuance of the product if she intends to become or suspects that she is pregnant.
Administration of benzodiazepines in the last trimester of pregnancy or during labour has been reported to produce irregularities in the foetal heart rate, and hypotonia, poor sucking and hypothermia and moderate respiratory depression in the neonate.
Moreover, infants born to mothers who took benzodiazepines chronically during the latter stages of pregnancy may have developed physical dependence and may be at some risk of developing withdrawal symptoms in the postnatal period.
Breast-feeding
There is insufficient information on the excretion of flurazepam and/or metabolites in human milk. However, in common with other benzodiazepines, its passage into breast milk might be expected. The use of Dalmane in mothers who are breast-feeding is not recommended.
4.7 Effects on ability to drive and use machines
Patients should be advised that, like all medicaments of this type, Dalmane might modify patients' performance at skilled tasks (driving, operating machinery, etc.) to a varying degree depending upon dosage, administration, and sleep pattern and individual susceptibility. Patients should further be advised that alcohol may intensify any impairment, and should therefore be avoided during treatment.
This medicine can impair cognitive function and can affect a patient’s ability to drive safely. This class of medicine is in the list of drugs included in regulations under 5a of the Road Traffic Act 1988. When prescribing this medicine, patients should be told:
• The medicine is likely to affect your ability to drive
• Do not drive until you know how the medicine affects you
• It is an offence to drive while under the influence of this medicine
• However, you would not be committing an offence (called ‘statutory defence’) if:
- The medicine has been prescribed to treat a medical or dental problem and
- You have taken it according to the instructions given by the prescriber and in the information provided with the medicine and
- It was not affecting your ability to drive safely.
4.8 Undesirable effects
Common adverse effects include drowsiness during the day, numbed emotions, reduced alertness, confusion, fatigue, headache, dizziness, muscle weakness, ataxia and double vision. These phenomena are dose-related and are likely to be uncommon with the recommended dosage; they occur predominantly at the start of therapy and usually disappear with repeated administration. The elderly are particularly sensitive to the effects of centrally depressant drugs.
Other adverse effects are rare and include vertigo, hypotension, gastrointestinal upsets, skin rashes, visual disturbances, changes in libido, and urinary retention. Isolated cases of blood dyscrasias and jaundice have also been reported.
Occasionally patients treated with Dalmane experience a bitter after-taste. 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.
4.9 Overdose
When taken alone in overdosage Dalmane presents few problems in management and should not present a threat to life unless combined with other CNS depressants (including alcohol).
Symptoms:
Special attention should be paid to respiratory and cardiovascular functions in intensive care. Overdose of benzodiazepines is usually manifested by degrees of central nervous system depression ranging from drowsiness to coma. In mild cases, symptoms include drowsiness, mental confusion, dysarthria and lethargy; in more serious cases, symptoms may include ataxia, hypotonia, hypotension, respiratory depression, rarely coma and very rarely death.
Management:
In the management of overdose with any medicinal product, it should be borne in mind that multiple agents might have been taken.
Following overdose with oral benzodiazepines, vomiting should be induced if the patient is conscious or gastric lavage undertaken with the airway protected if the patient is unconscious. If there is no advantage in emptying the stomach, activated charcoal should be given to reduce absorption.
The value of dialysis has not been determined. Flumazenil is a specific IV antidote for use in emergency situations. Patients requiring such intervention should be monitored closely in hospital (see separate prescribing information).
If excitation occurs, barbiturates should not be used.
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Hypnotics and Sedatives, Benzodiazepine derivatives,
ATC code: N05CD01
Flurazepam is a psychotropic substance from the class of 1,4-benzodiazepines. Onset of sedative effects occurs within 30 minutes. Due to accumulation of the active metabolite N1-desalkyl-flurazepam peak response is not observed before night 2-3 of treatment.
Flurazepam binds to specific benzodiazepine receptors located on GABA-ergic neurones and potentiates the inhibitory actions of GABA-ergic neurones in the nervous system.
After prolonged flurazepam treatment, development of tolerance has been observed. Chronic benzodiazepine use leads to compensating changes in the central nervous system. GABAA receptors may become less responsive to the continuing acute effects of benzodiazepines, either as a result of adaption in the GABAA receptor itself, intracellular mechanisms, or changes in the neurotransmitter systems. Probably multiple adaptive mechanisms simultaneously co-exist.
An increase in intensity and incidence of CNS toxicity with age has been observed, especially at high doses. Therefore the initial dose of Dalmane in elderly should not exceed 15 mg (see section 4.2) The increased CNS toxicity in elderly seems to be the result of the combination of pharmacokinetic and pharmacodynamic factors.
Under the treatment with 15 and 30 mg flurazepam impairment of psychomotor and cognitive performance was observed in several investigations. Especially the driving ability is affected (see section 4.7) In elderly patients the effect is more pronounced.
5.2 Pharmacokinetic properties
The pharmacokinetic properties of Dalmane make it particularly indicated for patients whose total duration of sleep is less than adequate. The dosage of the drug is important in balancing the duration of effect with the occurrence of residual effects.
Absorption:
Flurazepam hydrochloride is rapidly and almost completely absorbed after oral administration. Maximum plasma concentrations were measured after 1 to 3 hours. The maximum plasma concentrations of the two pharmacologically active major metabolites N1-
hydroxyethyl-flurazepam and N1-desalkyl flurazepam were observed after 1 to 4 hours and 0.5 to 96 hours, respectively. In most subjects, the N1-desalkyl-flurazepam concentration reached a plateau value after 1 to 24 hours. The maximum plasma concentration of N1-hydroxyethyl-flurazepam ranges between 6 and 28 ng/ml and of N1-desalkyl-flurazepam ranges between 5 and 40 ng/ml after a single oral dose.
Distribution:
Flurazepam undergoes considerable first-pass metabolism.
The plasma protein binding is high for flurazepam (83%) and N1-desalkyl-flurazepam (96.5%) and lower for N1-hydroxyethyl-flurazepam (65%).
Taking flurazepam hydrochloride over a period of 15 days the N1-desalkyl-flurazepam accumulated. The plasma concentrations were 7.5 times higher on the 15th day versus the 1st day.
The concentration of flurazepam and its metabolites is 2 times (for N1-hydroxyethyl-flurazepam), 7 times (for flurazepam) or 8 times (for N1-desalkyl-flurazepam) higher in cerebrospinal fluid compared to plasma.
In animal models, flurazepam was eliminated from serum in biphasic fashion, consistent with two-compartment model and volume of distribution was between 2.65 and 5.5 l/kg.
Flurazepam and/or active metabolites cross the placental barrier in rodents. Human data are not available.
No information concerning secretion of flurazepam and metabolites in the breast milk are available. However in common with other benzodiazepines, its passage into breast milk might be expected.
Biotransformation:
The plasma half-life for flurazepam and N1-hydroxyethyl-flurazepam was 3.1 hours and 2.3 to 3.4 hours, respectively. For N1-desalkyl-flurazepam, the corresponding values were 19 to 133 hours. In elderly subjects (66 - 85 years) still higher values for N1-desalkyl-flurazepam were obtained (71-289 hours). The metabolites are further conjugated to glucuronides and / or sulfates for renal excretion
Elimination:
Flurazepam monohydrochloride and its metabolites are eliminated primarily by renal excretion (about 80%). The major urinary metabolite, N1-hydroxy ethyl-flurazepam as glucuronide/sulphate conjugate accounts for 20-55% of an orally administered dose.
5.3 Preclinical safety data
Mutagenic and tumourigenic potential:
There is insufficient data available to evaluate the genotoxic potential of flurazepam. The limited studies performed to date showed no evidence of genotoxicity.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
15 mg capsules contain the following excipients: lactose, talc purified, magnesium stearate, black iron oxide E172, titanium dioxide E171 and yellow iron oxide E172.
6.2. Incompatibilities
Not applicable.
6.3. Shelf Life
Amber glass bottles and plastic adept containers - 5 years.
PVDC blister packs - 3 years.
Polythene bags in tins and small HDPE bottles - 2 years. White securitainers - 1 year.
6.4. Special Precautions for Storage
Dalmane capsules should be stored in a dry place with a recommended maximum storage temperature of 25°C.
6.5 Nature and contents of container
PVDC blister packs, amber glass bottles, polythene bags in tins, plastic adept containers, white securitainers and small HDPE bottles containing 30 capsules.
Not all pack sizes may be marketed.
6.6 Special precautions for disposal and other handling
No special requirements for disposal.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
7. Marketing Authorisation Holder
Meda Pharmaceuticals Ltd Skyway House Parsonage Road Takeley
Bishop’s Stortford CM22 6PU
8. MARKETING AUTHORISATION NUMBER
PL 15142/0016
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
15/08/2001
10 DATE OF REVISION OF THE TEXT
02/06/2015