Product image of Lexotan (Bromazepam) supplied by GNH India

Lexotan

Active Ingredient:
Bromazepam
Origin:
EU

Lexotan (Bromazepam)

Bromazepam, the active ingredient in Lexotan, is a benzodiazepine presented as an oral tablet for oral use. It is prescribed for the short‑term relief of anxiety symptoms in adults. It belongs to the class of central nervous system depressants that enhance the activity of the inhibitory neurotransmitter gamma‑aminobutyric acid (GABA).

GNH India supplies Lexotan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to global quality standards and provides regulatory documentation for import and distribution.

Manufacturer / TM Owner

Cheplapharm Arzneimittel Gmbh

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Indications & Clinical Uses

  • Bromazepam acts on the central nervous system to alleviate anxiety-related conditions.
  • Generalized anxiety disorder: reduces excessive worry and tension during short‑term treatment.
  • Panic disorder: helps diminish the frequency and intensity of panic attacks when used briefly.
  • Situational anxiety (e.g., before medical procedures): provides rapid calming effect to facilitate cooperation.
  • Anxiety associated with depression: eases nervousness and tension when used as an adjunct to antidepressants.
  • Pre‑operative anxiety: lowers nervousness before surgery to improve patient comfort.
  • Anxiety‑related insomnia: facilitates sleep onset in patients with transient anxiety‑induced sleeplessness.

How It Works

  • Bromazepam binds to a specific site on the gamma‑aminobutyric acid type A (GABA‑A) receptor complex, acting as a positive allosteric modulator. By enhancing the affinity of GABA for its receptor, it increases chloride ion influx, hyperpolarising neuronal membranes and producing a net inhibitory effect on central nervous system activity, which manifests as anxiolysis, sedation and muscle relaxation. The resultant decrease in neuronal excitability underlies its therapeutic action in anxiety disorders.

Side Effects

Bromazepam may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Drowsiness
  • Fatigue
  • Dizziness
  • Impaired coordination
  • Headache

Serious or Rare Side Effects

  • Dependence and withdrawal syndrome
  • Respiratory depression, especially with other depressants
  • Severe allergic reactions (e.g., rash, swelling, anaphylaxis)
  • Paradoxical agitation or aggression

Precautions & Warnings

When prescribing bromazepam, clinicians should observe several precautionary measures to minimise risk.

  • Dose adjustment in elderly: start with a lower dose and monitor for excessive sedation.
  • Renal or hepatic impairment: consider dose reduction and assess liver function regularly.
  • Concomitant CNS depressants: avoid or limit use to reduce additive sedation.
  • History of substance abuse: evaluate risk of dependence before initiating therapy.
  • Pregnancy and lactation: use only if potential benefit outweighs risk; discuss with obstetrician.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protected from moisture and light.

Avoid Interactions

Bromazepam can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Alcohol: may cause profound sedation and respiratory depression.
  • Opioids (e.g., morphine, oxycodone): risk of additive CNS depression and life‑threatening respiratory depression.
  • Other benzodiazepines or hypnotics: can lead to excessive sedation and impaired psychomotor function.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): increase bromazepam plasma concentrations, raising toxicity risk.
  • Central nervous system depressants (e.g., antihistamines, antipsychotics): enhance sedative effects.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce bromazepam levels and efficacy.
  • Selective serotonin reuptake inhibitors (e.g., fluoxetine, sertraline): can increase sedation.
  • Antihistamines (e.g., diphenhydramine): may augment drowsiness.

Frequently Asked Questions

Lexotan contains bromazepam, a benzodiazepine prescribed for the short‑term relief of anxiety symptoms in adults. It is indicated for generalized anxiety disorder, panic attacks, situational anxiety and may be used as an adjunct for anxiety‑related insomnia.

Bromazepam binds to a specific site on the GABA‑A receptor complex, acting as a positive allosteric modulator. This enhances GABA’s inhibitory effect, increasing chloride influx, hyperpolarising neurons and reducing central nervous system activity, which produces anxiolysis and sedation.

The dose of Lexotan is individualized by the prescribing clinician based on the patient’s age, clinical condition and response. Only a qualified health professional can determine the appropriate strength, frequency and duration of therapy.

Safety of bromazepam in pregnancy or lactation has not been definitively established. It should be used only if the potential benefit justifies the possible risk to the fetus or infant, and decisions should be made in consultation with an obstetrician.

To order Lexotan, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and import documentation.

Lexotan (bromazepam) is a benzodiazepine, offering rapid anxiolytic effect through GABA‑A modulation. Compared with non‑benzodiazepine anxiolytics such as buspirone, bromazepam has a quicker onset but carries higher risk of dependence and sedation, requiring careful short‑term use.

Lexotan tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original packaging, protect from moisture and light, and store out of reach of children.

Lexotan is taken orally, usually with a glass of water. The tablet should be swallowed whole and not chewed or crushed, unless otherwise directed by a healthcare professional.

Serious risks include the development of physical dependence, withdrawal syndrome on abrupt discontinuation, respiratory depression when combined with other CNS depressants, and rare severe allergic reactions. Patients should be monitored closely for these events.

Lexotan is contraindicated in individuals with known hypersensitivity to bromazepam or other benzodiazepines, severe respiratory insufficiency, acute narrow‑angle glaucoma, and in patients with a history of severe substance abuse unless closely supervised.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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