Therapeutic/Pharmacologic Class of Drug: Anxiolytic.
Type of Dosage Form: Tablets.
Route of Administration: Oral.
Qualitative and Quantitative Composition: Active ingredient:

Pharmacodynamic Properties

Mechanism of Action: The central actions of benzodiazepines are mediated through an enhancement of the GABAergic neurotransmission at inhibitory synapses. In the presence of benzodiazepines the affinity of the GABA receptor for the neurotransmitter is enhanced through positive allosteric modulation resulting in an increased action of released GABA on the postsynaptic transmembrane chloride ion flux. At low dosage, Lexotanil® selectively reduces tension and anxiety. At high dosage, sedative and musclerelaxant properties appear.

Pharmacokinetic Properties

Absorption: Bromazepam is absorbed quickly and reaches peak plasma concentrationswithin 2 hours after oral administration. The absolute bioavailability of the bromazepam tablet is 60%. Food may decrease the bioavailability of bromazepam. During multiple dosing of bromazepam the extent of absorption remains constant; predictable steady-state concentrations are observed and confirm linear kinetics for the drug.

Distribution: After absorption, bromazepam is rapidly distributed in the body. On average, 70% of bromazepam is bound by hydrophobic interaction to plasma proteins; binding partners are albumin and ¬1-acid glycoprotein. The volume of distribution is around 50 litres.

Metabolism: Bromazepam is extensively metabolised in the liver. No metabolites with a half-life longer than that of the parent drug are formed. Quantitatively, two metabolites dominate: 3-hydroxy-bromazepam (less active than bromazepam) and 2-(2-amino-5-bromo-3-hydroxybenzoyl) pyridine (inactive). Bromazepam is metabolized, at least in part, through cytochrome P450 (CYP450). However, the specific CYP isozymes involved have not been identified. Nevertheless, the observations that a strong CYP3A4 inhibitor (itraconazole) and a moderate CYP2C9 inhibitor (fluconazole) had no effect on the pharmacokinetics of bromazepam suggest that these isozymes are not involved to a major extent. The pronounced interaction with fluvoxamine (see Interactions with other Medicinal Products and other Forms of Interaction–Pharmacokinetic drug-drug interaction) points to the co-involvement of CYP1A2.

Elimination: Bromazepam has an elimination half-life of about 20 hours and an elimination clearance of around 40ml/min. Metabolism is the key elimination pathway for the drug. The urinary recovery of intact bromazepam is only 2% and of the glucuronide conjugates of 3-hydroxy-bromazepam and 2-(-2-amino-5-bromo- 3-hydroxybenzoyl) pyridine is 27% and 40% of the administered dose respectively.

Pharmacokinetics in Special Populations

Elderly: Elderly patients may have significantly higher peak concentrations, a smaller volume of distribution, increased serum free fraction, lower clearance and hence also a prolonged elimination half-life. This indicates that steady-state concentrations of bromazepam at any given dosing rate will be on average nearly twice as high in an elderly subject as compared to a younger individual (see Special Dosage Instructions).

Preclinical safety

Carcinogenicity: Carcinogenicity studies conducted in rats did not reveal any evidence of a carcinogenic potential for bromazepam.

Mutagenicity: Bromazepam was not genotoxic in in vitro and in vivo tests.

Impairment of Fertility: Daily oral administration of bromazepam did not have any effect on the fertility and general reproductive performance of rats.

Teratogenicity: Increases in fetal mortality, an increase in the stillbirth rate and areduction in pup survival have been observed when bromazepam was given to pregnant rats. In studies on embryotoxicity/ teratogenicity no teratogenic effect was detected up to a dosage of 125 mg/kg/day. Following per os administration with doses of up to 50 mg/kg/day to pregnant rabbits a reduction in maternal weight gain, a reduction in fetal weight and an increase in the incidence of resorptions have been observed.

Other: Chronic toxicity: No deviations from normal were observed in long-term toxicology studies except for an increase in liver weight. Histopathological examination revealed centrolobular hepatocellular hypertrophy which was considered to be indicative of enzyme induction by bromazepam. Adverse effects observed after high doses were slight to moderate sedation, ataxia, isolated brief convulsive seizures, occasional elevation in serum alkaline phosphatase and a borderline increase in SGPT (ALT).


Tablets:3 mg.

  Dosage and Administration

Dosage and Administration
Standard dosage: Average dosing for outpatient therapy: 1.5–3 mg up to three times daily. Severe cases, especially in hospital: 6–12 mg two or three times daily. These amounts are general recommendations, and dosage should be individually determined. Treatment of outpatients should begin with low doses, gradually increasing to the optimum level. The duration of treatment should be as short as possible. The patient should be reassessed regularly and the need for continued treatment should be evaluated, especially in case the patient is symptom-free. The overall treatment generally should not be more than 8–12 weeks, including a tapering-off process. 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 with special expertise.

Special Dosage Instructions: Lexotanil® is usually not indicated in children, but if the physician feels Lexotanil® treatment is appropriate, then the dose should be adjusted to their low body weight (about 0.1–0.3 mg/kg body weight). Elderly patients (see Pharmacokinetics in Special Populations) and those with impaired hepatic function require lower doses because of individual variations in sensitivity and pharmacokinetics.

  Side Effects

Undesirable Effects

Post Marketing: Lexotanil® is well tolerated in therapeutic doses.
The following undesirable effects may occur:
Psychiatric Disorders: Confusional state, emotional disorder. These phenomena occur predominantly at the start of therapy and usually disappear with repeated administration. Libido disorders have been reported occasionally.

Depression: Pre-existing depression may be unmasked during benzodiazepine use. Paradoxical reactions such as restlessness, agitation, irritability, aggression, delusion, anger, nightmares, hallucinations, psychosis, inappropriate behaviour and other adverse behavioural effects are known to occur with benzodiazepines or benzodiazepine-like agents (see 2.4.2 Drug Abuse and Dependence). Should this occur, the use of the drug should be discontinued. They are more likely to occur in children and elderly patients than in other patients.

Dependence: Chronic use (even at therapeutic doses) may lead to the development of physical and psychic drug dependence: discontinuation of therapy may result in withdrawal or rebound phenomena (see 2.4.1 General [Warnings and Precautions] and 2.4.2 Drug Abuse and Dependence). Abuse of benzodiazepines has been reported.

Nervous System Disorders: Drowsiness, headache, dizziness, decreased alertness, ataxia. These phenomena occur predominantly at the start of therapy and usually disappear with repeated administration. Anterograde amnesia may occur using therapeutic dosages, the risk increasing at higher dosages. Amnestic effects may be associated with inappropriate behaviour.

Eye Disorders: Diplopia, this phenomenon occurs predominantly at the start of therapy and usually disappears with repeated administration.

Gastrointestinal Disorders: Gastrointestinal disorders have been reported occasionally.

Skin and Subcutaneous Tissue Disorders: Skin reactions have been reported occasionally.

Musculoskeletal and Connective Tissue Disorders: Muscle weakness, this phenomenon occurs predominantly at the start of therapy and usually disappears with repeated administration.

General Disorders and Administration Site Conditions: Fatigue, this phenomenon occurs predominantly at the start of therapy and usually disappears with repeated administration.

Injury, Poisoning and Procedural Complications: There have been reports of falls and fractures in benzodiazepine users. The risk is increased in those taking concomitant sedatives (including alcoholic beverages) and in the elderly.

Respiratory Disorders: Respiratory depression.

Cardiac Disorders: Cardiac failure including cardiac arrest

Ability to Drive and Use Machines
Sedation, amnesia and impaired muscular function may adversely affect the ability to drive or to use machinery. This effect is increased if the patient has taken alcohol.


Contraindications: Lexotanil® must not be administered to patients with known hypersensitivity to benzodiazepines, severe respiratory insufficiency, severe hepatic insufficiency (benzodiazepines are not indicated to treat patients with severe hepatic insufficiency as they may cause encephalopathy) or sleep apnea syndrome.

  Use in Pregnancy and Lactation

Use in Special Populations

Pregnancy: The safety of bromazepam for use in human pregnancy has not been established. A review of spontaneously reported adverse drug events shows no greater incidence than would be anticipated from a similar untreated population. An increased risk of congenital malformations associated with the use of minor tranquilisers (diazepam, meprobamate and chlordiazepoxide) during the first trimester of pregnancy has been suggested in several studies. Bromazepam should be avoided during pregnancy unless there is no safer alternative. 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 bromazepam during the last three months of pregnancy or during labour is allowed only in the event of a strict medical indication as, due to the pharmacological action of the product, effects on the neonate can be expected, such as hypothermia, hypotonia and moderate respiratory depression. 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 for developing withdrawal symptoms in the postnatal period.

Labour and Delivery: See Pregnancy.

Nursing Mothers: As benzodiazepines pass into breast milk, nursing mothers should not take Lexotanil®.

Pediatric Use: See Special Dosage Instructions.

Geriatric Use: See also Special Dosage Instructions Undesirable Effects and Pharmacokinetics in Special Populations.

Hepatic Impairment: See Special Dosage Instructions.

  Drug Interaction

Interactions with other Medicinal Products and other Forms of Interaction

Pharmacokinetic Drug-Drug Interaction (DDI): There is a possibility that compounds, which inhibit key oxidative hepatic enzymes may enhance the activity of benzodiazepines. Co-administration of cimetidine, a multi-CYP inhibitor, and possibly propranolol may prolong the elimination half-life of bromazepam through a substantially reduced clearance (with cimetidine: reduction by 50%). Combined administration with fluvoxamine, an inhibitor of CYP1A2, results in significantly increased bromazepam exposure (AUC, 2.4-fold) and elimination half-life (1.9-fold). Bromazepam does not induce oxidative hepatic enzymes at therapeutic doses.

Pharmacodynamic Drug-Drug Interaction (DDI):Enhanced effects on sedation, respiration and hemodynamics may occur when Lexotanil® is co-administered with any centrally acting depressants including alcohol. Alcohol should be avoided in patients receiving Lexotanil® (see General [Warnings and Precautions]). See Overdose for warning of other central nervous system depressants, including alcohol. In the case of narcotic analgesics enhancement of euphoria may also occur, leading to an increase in psychic drug dependence.

  Over Dosage


Symptoms: Benzodiazepines commonly cause drowsiness, ataxia, dysarthria and nystagmus. Overdose of Lexotanil® is seldom life-threatening if the drug is taken alone, but may lead to areflexia, apnea, hypotension, cardiorespiratory depression and coma. Coma, if it occurs, usually lasts a few hours but it may be more protracted and cyclical, particularly in elderly patients. Benzodiazepine respiratory depressant effects are more serious in patients with respiratory disease. Benzodiazepines increase the effects of other central nervous system depressants, including alcohol.

Treatment: Monitor the patient’s vital signs and institute supportive measures as indicated by the patient’s clinical state. In particular, patients may require symptomatic treatment for cardiorespiratory effects or central nervous system effects. Further absorption should be prevented using an appropriate method e.g. treatment within 1–2 hours with activated charcoal. If activated charcoal is used, airway protection is imperative for drowsy patients. In case of mixed ingestion gastric lavage may be considered, however, not as a routine measure. If CNS depression is severe consider the use of flumazenil (Anexate®), a benzodiazepine antagonist. This should only be administered under closely monitored conditions. It has a short half-life (about an hour), therefore patients administered flumazenil will require monitoring after its effects have worn off. Flumazenil is to be used with extreme caution in the presence of drugs that reduce seizure threshold (e.g. tricyclic antidepressants). Refer to the prescribing information for flumazenil (Anexate®), for further information on the correct use of this drug.

Drug Abuse and Dependence

Dependence: The use of benzodiazepines and benzodiazepinelike agents may lead to the development of physical and psychic dependence upon these products (see 2.6 Undesirable Effects). The risk of dependence increases with the dose and duration of treatment; it is also greater in patients with a medical history of alcohol and/or drug abuse.

Withdrawal: Once physical dependence has developed, termination of treatment will be accompanied by withdrawal symptoms. These may consist of headaches, diarrhea, muscle pain, extreme anxiety, tension, restlessness, confusion and irritability. In severe cases the following symptoms may occur: derealisation, depersonalisation, hyperacusis, numbness and tingling of the extremities, hypersensitivity to light, noise and physical contact, hallucinations or epileptic seizures (see 2.6 Undesirable Effects). Rebound anxiety, a transient syndrome whereby the symptoms that led to treatment with Lexotanil® recur in an enhanced form, may occur on withdrawal of treatment. It may be accompanied by other reactions including mood changes, anxiety or sleep disturbances and restlessness. Since the risk of withdrawal phenomena and rebound phenomena is greater after abrupt discontinuation of treatment, it is recommended that the dosage be decreased gradually.



Storage: This medicine should not be used after the expiry date (EXP) shown on the pack. Protect from light. Store in a dry place below 35 degree celcius.

  Commercial Pack

Packs: Each box contains 70 tablets. Keep out of reach of children.


Warnings and Precautions

General: Amnesia: Benzodiazepines may induce anterograde amnesia. Anterograde amnesia may occur using higher therapeutic dosages (documented at 6 mg), the risk increasing at higher dosages.
Duration of treatment: It may be useful to inform the patient when treatment is started that it will be of limited duration and to explain precisely how the dosage will be progressively decreased. It is important that the patient should be aware of the possibility of rebound phenomena that may occur while the drug is being discontinued (see Drug Abuse and Dependence).

General precautions: Concomitant use of alcohol/CNS depressants: The concomitant use of Lexotanil® with alcohol or/ and central nervous system (CNS) depressants should be avoided. Such concomitant use has the potential to increase the clinical effects of Lexotanil® possibly including severe sedation, clinically relevant respiratory and/or cardiovascular depression (see Interactions with other Medicinal Products and other Forms of Interaction).

Medical history of alcohol or drug abuse: Lexotanil® should be used with extreme caution in patients with a medical history of alcohol or drug abuse. The patient should be checked regularly at the start of treatment in order to minimise the dosage and/or the frequency of administration and to prevent overdose due to accumulation. When benzodiazepines are used, withdrawal symptoms may develop when changing to a benzodiazepine with a considerably shorter elimination half-life (see Drug Abuse and Dependence).

Tolerance: Some loss of response to the effects of Lexotanil® may develop after repeated use for a prolonged time. Benzodiazepines should not be used alone to treat depression or anxiety associated with depression (suicide may be precipitated in such patients). Benzodiazepines are not recommended for the primary treatment of psychotic illness.

Specific patient groups: In patients with myasthenia gravis who are prescribed Lexotanil®, care should be taken on account of pre-existing muscle weakness. Particular care is required in patients with chronic respiratory insufficiency due to the risk of respiratory depression. If containing lactose, patients with rare hereditary problems of galactose intolerance (the Lapp lactase deficiency or glucose-galactose malabsorption) should not take this medicine.

Version: 03/ CDS: 07

  • Lexotanil
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