Product image of Lasdul (Duloxetine) supplied by GNH India

Lasdul

Active Ingredient:
Duloxetine
Origin:
EU

Lasdul (Duloxetine)

Duloxetine, the active ingredient in Lasdul, is a serotonin‑norepinephrine reuptake inhibitor (SNRI) presented as an oral tablet for oral use. It is prescribed for several chronic pain and mood disorders in adult patients.

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

Manufacturer / TM Owner

Towa Pharmaceutical Europe S.L.

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Indications & Clinical Uses

Duloxetine acts on serotonin and norepinephrine pathways and is indicated for several psychiatric and pain conditions.

  • Major depressive disorder: reduces depressive symptoms and improves overall mood.
  • Generalized anxiety disorder: alleviates excessive worry and anxiety.
  • Diabetic peripheral neuropathic pain: lessens nerve‑related pain in diabetic patients.
  • Fibromyalgia: decreases widespread musculoskeletal pain and fatigue.
  • Chronic musculoskeletal pain: provides relief from persistent musculoskeletal discomfort.

How It Works

  • Duloxetine inhibits the reuptake of the neurotransmitters serotonin and norepinephrine at neuronal synapses, thereby increasing their extracellular concentrations. The enhanced serotonergic and noradrenergic signaling modulates pain pathways and mood regulation, contributing to its antidepressant, anxiolytic, and analgesic effects.

Side Effects

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

Common Side Effects

  • Nausea: transient stomach upset, often early in therapy.
  • Dry mouth: reduced salivation causing discomfort.
  • Dizziness: light‑headed sensation, especially when standing quickly.
  • Somnolence: increased sleepiness or fatigue.

Serious or Rare Side Effects

  • Suicidal thoughts: emergence of suicidal ideation, particularly in young adults.
  • Serotonin syndrome: potentially life‑threatening condition with agitation, hyperthermia, and muscle rigidity.
  • Severe liver injury: jaundice, dark urine, or elevated liver enzymes.
  • Hyponatremia: low blood sodium causing confusion or seizures.
  • Severe allergic reaction: rash, swelling, or difficulty breathing.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate specific risk factors and monitor patients closely.

  • Assess for suicidal ideation: monitor mood changes, especially during the first weeks.
  • Evaluate liver function: avoid use in patients with significant hepatic impairment.
  • Review concomitant serotonergic agents: increase risk of serotonin syndrome.
  • Monitor blood pressure: duloxetine may cause modest elevations.
  • Store at ambient temperature: keep below 25°C in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Duloxetine can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis and serotonin syndrome.
  • Serotonergic antidepressants (e.g., SSRIs, tricyclics): heightened serotonin toxicity.
  • Strong CYP1A2 inhibitors (e.g., fluvoxamine): may increase duloxetine plasma levels.

Moderate Interactions (Monitor Closely)

  • CYP2D6 substrates (e.g., codeine, tamoxifen): duloxetine may reduce their effectiveness.
  • Anticoagulants (e.g., warfarin): potential for increased bleeding risk.
  • NSAIDs or antiplatelet agents: may augment gastrointestinal bleeding risk.

Frequently Asked Questions

Lasdul contains duloxetine, an SNRI indicated for major depressive disorder, generalized anxiety disorder, diabetic peripheral neuropathic pain, fibromyalgia, and chronic musculoskeletal pain in adult patients.

Duloxetine blocks the reuptake of serotonin and norepinephrine at neuronal synapses, raising their levels in the central nervous system. This dual action helps regulate mood and modulate pain signaling pathways.

The appropriate dose of Lasdul is determined by the prescribing clinician based on the specific indication, patient characteristics, and response to therapy. Dosage adjustments are made according to clinical judgment.

Safety data for duloxetine in pregnancy and lactation are limited. Clinicians should weigh potential benefits against risks and consider alternative therapies when treating pregnant or nursing individuals.

To request Lasdul, 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 necessary import documentation.

Unlike selective serotonin reuptake inhibitors (SSRIs) that target only serotonin, Lasdul (duloxetine) also increases norepinephrine levels, offering additional benefit for certain pain conditions and potentially a different side‑effect profile.

Store Lasdul at ambient temperature, preferably below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure the container is tightly closed.

Lasdul is taken orally, usually with or without food, as directed by the prescriber. Swallow the tablet whole with a full glass of water; do not crush or chew unless specifically instructed.

Serious risks include the emergence of suicidal thoughts, serotonin syndrome, severe liver injury, hyponatremia, and rare but severe allergic reactions. Patients should be monitored closely for these events.

Lasdul is contraindicated in patients taking monoamine oxidase inhibitors, those with uncontrolled narrow‑angle glaucoma, severe hepatic impairment, or known hypersensitivity to duloxetine or any tablet excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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