Product image of Lambutrix (Lorazepam) supplied by GNH India

Lambutrix

Active Ingredient:
Lorazepam
Origin:
EU

Lambutrix (Lorazepam)

Lorazepam, the active ingredient in Lambutrix, is a benzodiazepine presented as a sterile injectable solution for intramuscular and intravenous use. It is employed to manage anxiety disorders, insomnia linked to anxiety, pre‑operative sedation, and status epilepticus in adult patients.

GNH India supplies Lambutrix as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Macure Healthcare Limited

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Indications & Clinical Uses

Lambutrix (lorazepam) acts on the central nervous system to alleviate conditions mediated by excessive neuronal excitation.

  • Anxiety disorders: reduction of excessive anxiety and associated physiological symptoms.
  • Insomnia associated with anxiety: facilitation of sleep onset and maintenance.
  • Preoperative sedation: provision of calmness and amnesia before surgical procedures.
  • Status epilepticus: rapid control of prolonged seizure activity when other measures are insufficient.

How It Works

  • Lorazepam enhances GABAergic neurotransmission by binding to the benzodiazepine site on GABA‑A receptors. This increases the frequency of chloride channel opening, leading to greater chloride influx, neuronal hyperpolarization, and reduced excitability throughout the central nervous system.

Side Effects

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

Common Side Effects

  • Drowsiness: feeling unusually sleepy or fatigued.
  • Dizziness: sensation of light‑headedness or imbalance.
  • Headache: mild to moderate cranial pain.
  • Muscle weakness: reduced muscular strength or coordination.
  • Nausea: feeling of queasiness or urge to vomit.
  • Blurred vision: temporary visual disturbances.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing requiring medical attention.
  • Severe hypotension: marked drop in blood pressure leading to faintness.
  • Paradoxical reactions: agitation, aggression, or hallucinations.
  • Dependence or withdrawal: signs of physical or psychological dependence with abrupt discontinuation.
  • Anaphylaxis: rare severe allergic reaction with rash, swelling, or airway compromise.
  • Hepatic dysfunction: abnormal liver enzyme elevations.

Precautions & Warnings

Lambutrix should be used with caution in specific clinical situations.

  • Pregnancy: Category D – potential risk to the fetus; avoid unless clearly needed.
  • Elderly patients: increased sensitivity; start with lower doses and monitor closely.
  • Renal or hepatic impairment: dose adjustment may be required due to altered clearance.
  • Concomitant CNS depressants: risk of additive sedation and respiratory depression.
  • History of substance abuse: higher potential for dependence; consider alternative therapy.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Lambutrix can interact with several drug classes, influencing its safety profile.

Major Interactions (Avoid)

  • Opioids: synergistic respiratory depression and profound sedation.
  • Barbiturates: enhanced CNS depression and risk of coma.
  • Alcohol: additive sedative effects and impaired psychomotor function.
  • Antifungals (e.g., ketoconazole): increased lorazepam plasma concentrations.
  • Macrolide antibiotics (e.g., erythromycin): elevated lorazepam levels.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs, SNRIs): possible increased sedation.
  • Antihistamines: additive drowsiness.
  • Anticonvulsants (phenytoin, carbamazepine): may reduce lorazepam efficacy.
  • Cimetidine: modest increase in lorazepam exposure.
  • Herbal supplements (St. John’s wort): potential reduction in therapeutic effect.

Frequently Asked Questions

Lambutrix, containing lorazepam, is indicated for the management of anxiety disorders, insomnia associated with anxiety, pre‑operative sedation, and the control of status epilepticus when rapid seizure termination is required.

Lorazepam binds to the benzodiazepine site on GABA‑A receptors, enhancing the inhibitory effect of the neurotransmitter GABA. This increases chloride ion influx, hyperpolarizing neurons and reducing excessive neuronal firing, which produces anxiolytic, sedative, anticonvulsant, and muscle‑relaxant effects.

The specific dose of Lambutrix is determined by the prescribing clinician based on the patient’s condition, age, weight, renal and hepatic function, and response to therapy. Dosing should follow the prescriber’s instructions and local clinical guidelines.

Lambutrix is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should be used only if the potential benefit justifies the risk. Lorazepam is excreted in breast milk; breastfeeding is generally not recommended while receiving this medication.

To order Lambutrix, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where applicable), and necessary import documentation.

Lambutrix (lorazepam) has a relatively intermediate onset of action and a longer duration compared with agents like midazolam. It is less lipid‑soluble, which reduces rapid redistribution and may result in a more predictable sedation profile, making it suitable for both acute seizure control and pre‑operative sedation.

Lambutrix should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Maintain the product in its original packaging until use to preserve sterility and potency.

Lambutrix is supplied as a sterile injectable solution and can be given intravenously or intramuscularly by a qualified healthcare professional. The route, rate, and volume of injection are determined by the prescriber according to the clinical indication.

The most serious risks include respiratory depression, severe hypotension, anaphylactic reactions, and the potential for dependence or withdrawal symptoms with prolonged use. Immediate medical attention is required if any signs of these serious adverse events occur.

Lambutrix is contraindicated in patients with known hypersensitivity to lorazepam or any benzodiazepine component, in individuals with acute narrow‑angle glaucoma, and in patients who are currently dependent on other CNS depressants without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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