Product image of Laroxyl (Amitriptyline Hydrochloride) supplied by GNH India

Laroxyl

Active Ingredient:
Amitriptyline Hydrochloride
Origin:
EU

Laroxyl (Amitriptyline Hydrochloride)

Amitriptyline Hydrochloride, the active ingredient in Laroxyl, is a tricyclic antidepressant presented as an oral tablet for oral use. It treats major depressive disorder and is also prescribed for neuropathic pain, migraine prophylaxis, and certain anxiety disorders in adult patients.

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

Manufacturer / TM Owner

Teofarma S.R.L.

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Indications & Clinical Uses

Laroxyl, a tricyclic antidepressant, is employed in several psychiatric and pain‑related conditions.

  • Major depressive disorder: alleviates depressive symptoms and improves mood in adult patients.
  • Neuropathic pain: reduces pain intensity and improves functional ability in peripheral neuropathy.
  • Migraine prophylaxis: decreases frequency and severity of migraine attacks.
  • Anxiety disorders: helps control excessive worry and associated physical symptoms.

How It Works

  • Amitriptyline hydrochloride blocks the reuptake of norepinephrine and serotonin, increasing their synaptic concentrations. It also antagonizes muscarinic, histamine H1, and alpha‑adrenergic receptors, contributing to its antidepressant, analgesic, and anti‑migraine effects while influencing autonomic and central nervous system activity.

Side Effects

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

Common Side Effects

  • Dry mouth: reduced salivary flow causing discomfort.
  • Constipation: slowed gastrointestinal motility.
  • Drowsiness: sedation especially after initial dosing.
  • Weight gain: increased appetite and metabolic changes.

Serious or Rare Side Effects

  • Cardiac arrhythmia: irregular heart rhythm, particularly in patients with pre‑existing heart disease.
  • Seizures: heightened risk at high doses or in susceptible individuals.
  • Suicidal thoughts: emergence or worsening of suicidal ideation, especially early in therapy.

Precautions & Warnings

Before initiating Laroxyl, clinicians should evaluate several safety aspects.

  • Cardiac assessment: review history of heart disease and consider ECG monitoring.
  • Suicidal risk: monitor for emergence of suicidal thoughts, particularly in young adults.
  • Discontinuation: avoid abrupt cessation to reduce withdrawal symptoms.
  • Elderly patients: start with low doses and watch for anticholinergic effects.
  • MAO inhibitor use: ensure a minimum 14‑day washout period before starting.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Amitriptyline interacts with several medicines; some require avoidance while others need close monitoring.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors: risk of hypertensive crisis and serotonin syndrome.
  • Selective serotonin reuptake inhibitors: increased serotonin levels may precipitate serotonin syndrome.
  • Other tricyclic antidepressants: additive cardiotoxic and anticholinergic effects.

Moderate Interactions (Monitor Closely)

  • Anticholinergic drugs: heightened anticholinergic burden may worsen dry mouth, constipation, and urinary retention.
  • CNS depressants (e.g., benzodiazepines, alcohol): enhanced sedation and respiratory depression.
  • Diuretics: may potentiate orthostatic hypotension.

Frequently Asked Questions

Laroxyl contains amitriptyline hydrochloride and is prescribed for major depressive disorder, neuropathic pain, migraine prevention, and certain anxiety disorders. It helps improve mood, reduce pain signals, and lower the frequency of migraine attacks in adult patients.

Amitriptyline inhibits the reuptake of norepinephrine and serotonin, raising their levels in the brain. It also blocks muscarinic, histamine H1, and alpha‑adrenergic receptors, which together produce antidepressant, analgesic, and anti‑migraine effects while influencing autonomic functions.

The dosage of Laroxyl is individualized. A qualified prescriber determines the appropriate strength, frequency, and duration based on the patient’s condition, response, and tolerance. Patients should follow the prescribing clinician’s instructions without self‑adjusting the dose.

Safety data for amitriptyline in pregnancy and lactation are limited. Clinicians weigh potential benefits against possible risks to the fetus or infant. Generally, the drug is used only if clearly needed, and breastfeeding mothers should discuss alternatives with their healthcare provider.

To request Laroxyl, 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, and any necessary import documentation.

The primary alternatives to amitriptyline are selective serotonin reuptake inhibitors (SSRIs). While SSRIs primarily increase serotonin and have a more favorable side‑effect profile, amitriptyline’s broader receptor activity can be advantageous for chronic pain and migraine but may cause more anticholinergic effects.

Laroxyl tablets should be stored at room temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

Laroxyl is taken orally, usually with a glass of water. It can be taken with or without food, although taking it with food may reduce gastrointestinal upset. Tablets should be swallowed whole and not crushed or chewed unless directed by a physician.

Serious risks include cardiac arrhythmias, seizures, severe hypotension, and the emergence of suicidal thoughts or behaviors, especially during the initial treatment period. Patients should seek immediate medical attention if they experience palpitations, fainting, seizure activity, or worsening mood.

Laroxyl is contraindicated in patients with known hypersensitivity to amitriptyline or other tricyclic antidepressants, recent myocardial infarction, uncontrolled narrow‑angle glaucoma, and those currently taking monoamine oxidase inhibitors. Caution is also advised for individuals with severe liver disease or a history of seizures.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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