Oxazepam Tablets 15mg
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Oxazepam Tablets 15mg
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Oxazepam tablets containing oxazepam 15mg.
Oxazepam (INN, BAN) is chemically defined as 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepine-2-one.
3 PHARMACEUTICAL FORM
Oxazepam Tablets 15mg are white round tablets, 6.5mm in diameter, having flat faces with bevelled edges. A breakbar on one face and “15” on the other.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Oxazepam is indicated for the short term relief (2-4 weeks) of anxiety that is disabling or subjecting the individual to unacceptable distress, occurring alone or in association with insomnia or short-term psychosomatic, organic and psychotic illness.
The use of benzodiazepines to treat short-term anxiety is considered to be inappropriate.
4.2 Posology and method of administration Posology
Dosage and duration of therapy should be individualised and all patients receiving oxazepam should be carefully monitored and re-evaluated before any extension of the treatment period. Long-term chronic use is not recommended.
As an anxiolytic, the lowest effective dose should be employed for the shortest time possible. Dosage regimes should not exceed beyond 4 weeks and treatment should be withdrawn gradually to minimise possible withdrawal symptoms (See Special Warnings and Precautions for Use).
Please note that in patients with renal or hepatic impairment, lower doses may be sufficient (see Special Warnings and Precautions for Use).
Adults:
• Anxiety - one to two 15mg tablets three (or four) times daily
• Insomnia associated with anxiety - In most cases, 15-25mg dose taken 1 hour before retiring. This may be increased to a maximum of 50mg where necessary
Elderly or patients who are particularly sensitive to the effects of benzodiazepines:
10-20mg three or four times daily
Children:
Oxazepam is not recommended for the treatment of children
Method of Administration
Oral administration
4.3 Contraindications
• Hypersensitivity to benzodiazepines including Oxazepam Tablets or their components
• Chronic psychosis
• Phobic or obsessional states
• Respiratory depression
• Sleep apnoea syndrome
• Myasthenia gravis
• Acute pulmonary insufficiency
• Severe hepatic insufficiency
4.4 Special warnings and precautions for use Tolerance
Patients should be advised that since their tolerance for alcohol and other CNS depressants will be diminished in the presence of oxazepam, these substances should either be avoided or taken in reduced dosage.
Some loss of efficacy to the hypnotic effects of short-acting benzodiazepines may develop after repeated use for a few weeks.
Dependance
The use of benzodiazepines may lead to physical and psychological dependence - the risk of this increases with higher doses and/or longer use; it is also greater in patients with a history of alcoholism or drug abuse, or in patients with significant personality disorders.
Dependence may lead to withdrawal symptoms (see Undesirable Effects), especially if treatment is discontinued abruptly.
It may be useful to inform the patient that treatment will be of limited duration and that it will be discontinued gradually. The patient should also be made aware of the possibility of "rebound" phenomena to minimise anxiety should they occur.
Abuse of benzodiazepines has been reported.
Amnesia
Benzodiazepines may induce anterograde amnesia. This condition usually occurs several hours after ingestion therefore patients should ensure that they will be able to have a period of uninterrupted sleep which is sufficient to allow dissipation of drug effect (e.g., 7-8 hours) wherever possible.
Psychiatric and paradoxical reaction
Reactions like restlessness, agitation, irritability, aggressiveness, delusion, rages, nightmares, hallucinations, psychoses, inappropriate behaviour and other adverse behavioural effects are known to occur when using benzodiazepines. Should this occur, use of the medicinal product should be discontinued. They are more likely to occur in children and the elderly.
Special patient groups
Oxazepam is not intended for the primary treatment of psychotic illness or depressive disorders, and should not be used alone to treat depressed patients. The use of benzodiazepines may have a disinhibiting effect and may release suicidal tendencies in depressed patients. Also, pre-existing depression may emerge during benzodiazepine use.
Caution should be used in the treatment of patients with acute narrow-angle glaucoma.
Patients with impaired renal or hepatic function should be monitored frequently and have their dosage adjusted carefully according to response. Lower doses may be sufficient in these patients. The same precautions apply to elderly or debilitated patients and patients with chronic respiratory insufficiency.
Benzodiazipines are not indicated to treat patients with severe hepatic impairment as they may precipitate encephalopathy, renal impairment, muscle weakness or porphyria
Benzodiazepines should not be given to children without careful assessment of the need to do so; the duration of treatment must be kept to a minimum.
Some patients taking benzodiazepines have developed a blood dyscrasia, and some have had elevations in liver enzymes. Periodic haematologic and liver-function assessments are recommended where repeated courses of treatment are considered clinically necessary.
Although hypotension has occurred only rarely, benzodiazepines should be administered with caution to patients in whom a drop in blood pressure might lead to cardiovascular or cerebrovascular complications. This is particularly important in elderly patients.
Patients with rare heriditary problems of galactose intolerance, the Lapp lactose deficiency or glucose-galactose malabsorption should not take this medicines.
4.5 Interaction with other medicinal products and other forms of interaction
The following drug interactions with oxazepam should be considered:
• Enhancement of other CNS depressant drugs such as barbiturates, antipsychotics, sedatives/hypnotics, anxiolytics, antidepressants, narcotic analgesics (enhancement of euphoria may also occur, leading to an increase in psychic dependence), sedative antihistamines, anticonvulsants, anaesthetics, lofexidine, nabilone and tizanidine.
• Concomitant use of alcohol is not recommended. The sedative effects may be enhanced when oxazepam is used in combination with alcohol. This will affect the ability to drive or use machines.
• Compounds which inhibit certain hepatic enzymes (particularly cytochrome P450) may enhance the activity of benzodiazepines. To a lesser degree this also applies to benzodiazepines which are metabolised only by conjugation.
• Oestrogen-containing contraceptives (concurrent use may cause a decrease in plasma levels of oxazepam)
• Antibacterials (Rifampicin may increase the metabolism of oxazepam)
• Antivirals (concurrent use of zidovudine with benzodiazepines may decrease Zidovudine clearance. Ritonavir may inhibit benzodiazepine hepatic metabolism). The clinical significance of these interactions has yet to be established.
• Antipileptic drugs (concurrent use of phenytoin may cause oxazepam serum levels to fall. Side effects may be more evident with hydantoins or barbiturates).
• Antihypertensives (enhanced hypotensive effects, enhances sedative effect with alpha blockers or moxonidine)
• Dopaminergics (concurrent use with benzodiazepines may decrease the therapeutic effects of levodopa).
• Baclofen (enhanced sedative effect)
• Probenecid (may increase effects and possibility of excessive sedation).
4.6 Fertility, pregnancy and lactation Women of childbearing potential
If the drug is prescribed to a woman of childbearing potential, she should be warned to contact her physician about stopping the drug if she intends to become, or suspects that she is, pregnant.
Pregnancy
Benzodiazepines should not be used during pregnancy, especially during the first and last trimesters. Benzodiazepines may cause foetal damage when administered to pregnant women.
There is a possibility that infants born to mothers who take benzodiazepines chronically during the later stages of pregnancy may develop physical dependence. The infant may also develop withdrawal symptoms during the postnatal period such as hypoactivity, hypotonia, hypothermia, respiratory depression, apnoea, feeding problems, and impaired metabolic response to cold stress.
Breastfeeding
The concentration of oxazepam and its conjugate in human breast milk is approximately 10% of the plasma level. Therefore, oxazepam should not be administered to breast-feeding mothers.
4.7 Effects on Ability to Drive and Use Machines
Sedation, amnesia, dizziness and impaired muscular function may adversely affect the ability to drive or use machines. If insufficient sleep occurs, the likelihood of impaired alertness may be increased (see also Interactions).
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
Adverse reactions, when they occur, are usually observed at the beginning of therapy and generally decrease in severity or disappear with continued use or upon decreasing the dose.
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Blood and lymphatic disorders |
Blood dyscrasias, leucopenia |
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Psychiatric disorders |
Mild drowsiness*, disorientation, dreams, jnightmares, |
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lethargy, amnesia (see below), mild excitatory effects with stimulation of affect**, numbed emotions, reduced alertness, frestlessness, fagitation, firritability, fdelusions, frages, fpsychoses, finappropriate behaviour, behavioural adverse effects including paradoxical faggressive outbursts, excitement, fhallucinations, confusion, uncovering of depression with suicidal tendencies.*** | |
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Nervous system disorders |
Dizziness, light-headedness*, ataxia, vertigo, headache, syncope, slurred speech, tremor, dysarthria |
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Eye disorders |
Blurred vision, double vision |
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Vascular disorders |
Hypotension |
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Gastrointestinal disorders |
Nausea, salivation changes, gastrointestinal disorders |
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Hepatobiliary disorders |
Increased liver enzymes, jaundice |
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Skin and subcutaneous tissue disorders |
Minor diffuse skin rashes (morbilliform, urticarial and macropapular) |
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Musculoskeletal and connective tissue disorders |
Muscle weakness |
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Renal and urinary disorders |
Incontinence, urinary retention |
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Reproductive system and breast disorders |
Altered libido |
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General disorders and administration site conditions |
Fever, oedema, fatigue |
* = Commonly seen in the first few days of therapy. If this becomes troublesome, dosage should be reduced
** = Reported in psychiatric patients and usually occur within the first few weeks of therapy
*** = Extreme caution should therefore be exercised in prescribing benzodiazepines to patients with
personality disorders
f = more likely to occur in children and the elderly_
Amnesia
Anterograde amnesia may occur using therapeutic dosages, the risk increasing at higher dosages and may lead to the patient exhibiting inappropriate behaviour.
Dependance
When used at the appropriate recommended dosage for short-term treatment of anxiety, the dependence potential of oxazepam is low. However, the risk of dependence is increased with higher doses and/or longer use; it is also greater in patients with a history of alcoholism or drug abuse, or in patients with significant personality disorders. (see Special Warnings and Precautions for Use)
Withdrawal
As with all benzodiazepines, withdrawal may be associated with physiological and psychological symptoms including depression, persistent tinnitus, involuntary movements, paraesthesia, perceptual changes, confusion, convulsions, muscle cramps, abdominal cramps and vomiting.
Symptoms such as anxiety, depression, headache, insomnia, tension and sweating have been reported following abrupt discontinuation of benzodiazepines and these symptoms may be difficult to distinguish from the original symptoms of anxiety.
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
Overdosage 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, atacia, dysarthia, nystagmus and lethargy. In more serious cases, symptoms may include ataxia, hypotension, hypotonia, respiratory depression and rarely coma.
As with other benzodiazepines, overdose should not present a threat to life unless combined with other CNS depressants (including alcohol).
Following overdose with oral benzodiazepines, induced vomiting and/or gastric lavage should be undertaken (if ingestion was recent). Alternatively (if there is no advantage in emptying the stomach), activated charcoal may be effective in reducing absorption (50mg for adults and 10-15mg for children if they have taken more than 1mg/kg within 1 hour, provided they are not too drowsy). Special attention should be paid to vital signs including respiratory and cardiovascular functions in extensive care. Supported measures are indicated depending on the patients clinical state. The patient is likely to sleep and therefore a clear airway should be maintained.
Hypotension, though unlikely, may be controlled with noradrenaline. The dialysability of oxazepam is minimal.
Flumazenil (Anaxate), a benzodiazepine antagonist, is available however should rarely be required. It has a short half-life (about an hour). Flumazenil is NOT TO BE USED IN A MIXED OVERDOSE OR AS A “DIAGNOSTIC” TEST.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
ATC code: N05B A
Oxazepam is a benzodiazepine with anxiolytic, sedative and hypnotic properties and possibly muscle relaxant and anticonvulsant characteristics. It acts by potentiation of the inhibitory effect of gamma-aminobutyrate by binding to specific sites of the brain stem reticular formation and other parts of the CMS.
5.2 Pharmacokinetic properties
Oxazepam is rapidly and almost completely absorbed from the gastrointestinal tract and is highly protein bound (approx.. 90%). Peak serum levels are reached in 1-5 hours and it has been reported to have a half-life of 6-20 hours. It is the ultimate pharmacologically active metabolite of diazepam and is metabolised by a simple one-step process to a pharmacologically inert compound, glucuronide.
Oxazepam crosses the placental barrier and is excreted in breast milk; lethargy and weight loss may occur in breast fed infants.
5.3 Preclinical safety data
Acute oral LD50 in mice is greater than 5000 mg/kg.
Fatty metamorphosis of the liver has been noted in six-week toxicity studies in rats given this product at 0.5% of the diet. Such accumulations of fat are considered reversible, since no liver necrosis or fibrosis is seen.
In vitro mutagenicity reports on Oxazepam are inconclusive.
In a carcinogenicity study, oxazepam was administered with diet to rats for two years. Male rats receiving 30 times the maximum human dose showed a statistical increase, when compared to controls, in benign thyroid follicular cell tumours, testicular interstitial cell adenomas, and prostatic adenomas. An earlier published study reported that mice fed dietary dosages of 35 or 100 times the human daily dose of oxazepam for 9 months developed a dose-related increase in liver adenomas. In an independent analysis of some of the microscopic slides from this mouse study, several of these tumours were classified as liver carcinomas. At this time, there is no evidence that clinical use of oxazepam is associated with tumours.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Lactose (hydrous), maize starch and magnesium stearate.
6.2 Incompatibilities
None known
6.3 Shelf life
36 months.
6.4 Special precautions for storage
Store in a dry place below 25 °C.
6.5 Nature and contents of container
1. Blister packs of PVC backed by hard tempered aluminium foil of 28, 30, 56, 60 or 100 tablets.
2. Securitainers of 28, 30, 56, 60 or 500 tablets.
6.6 Special precautions for disposal
Not applicable
7. MARKETING AUTHORISATION HOLDER
Genus Pharmaceuticals Holdings Limited T/A Genus Pharmaceuticals Linthwaite,
Huddersfield,
HD7 5QH, UK
8 MARKETING AUTHORISATION NUMBER(S)
PL 17225/0015
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
01/10/1999 / 06/03/2003
10 DATE OF REVISION OF THE TEXT
14/01/2015