Product image of Levotuss (Levodropropizine) supplied by GNH India

Levotuss

Active Ingredient:
Levodropropizine
Origin:
EU

Levotuss (Levodropropizine)

Levodropropizine, the active ingredient in Levotuss, is a peripherally acting antitussive presented as an oral formulation for oral use. It relieves dry, non‑productive coughs in adults and children when appropriate.

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

Manufacturer / TM Owner

Dompé Farmaceutici S.P.A.

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Indications & Clinical Uses

Levodropropizine acts on the peripheral cough pathway to provide symptomatic relief of cough.

  • Dry cough: reduces frequency and intensity of coughing episodes.
  • Non‑productive cough: suppresses the cough reflex without affecting mucus clearance.
  • Upper respiratory tract infection‑related cough: offers symptomatic relief of irritation‑driven cough.

How It Works

  • Levodropropizine exerts its antitussive effect by inhibiting the peripheral release of sensory neuropeptides such as substance P from airway afferent nerves, thereby lowering the sensitivity of cough receptors in the respiratory tract. The drug does not bind to opioid receptors and its action remains localized to the airway mucosa, providing cough suppression with minimal central sedation.

Side Effects

Levodropropizine is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Nausea: mild stomach upset reported by some users.
  • Dizziness: transient light‑headedness.
  • Headache: occasional mild headache.
  • Gastrointestinal discomfort: mild abdominal pain or dyspepsia.
  • Taste alteration: temporary change in taste perception.
  • Somnolence: mild sleepiness.

Serious or Rare Side Effects

  • Allergic reactions: rash, itching, or urticaria.
  • Angioedema: swelling of face, lips, or tongue.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatic enzyme elevation: signs of liver dysfunction.
  • Anaphylaxis: rare life‑threatening hypersensitivity.
  • Neutropenia: low white blood cell count.

Precautions & Warnings

When using Levotuss, consider the following precautions to ensure safe use.

  • Age restrictions: use in children only under medical supervision and according to prescribed age limits.
  • Hepatic impairment: dose adjustment may be required; monitor liver function.
  • Concomitant CNS depressants: caution as additive sedation may occur.
  • Known hypersensitivity: avoid if allergic to levodropropizine or excipients.
  • Pregnancy and breastfeeding: safety not established; use only if benefit outweighs risk.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levodropropizine may interact with other medicines; be aware of the following.

Major Interactions (Avoid)

  • Other antitussives (e.g., codeine, dextromethorphan): additive cough suppression and increased risk of sedation.
  • Strong CYP3A4 inhibitors (if metabolized via this pathway): may raise levodropropizine plasma levels.

Moderate Interactions (Monitor Closely)

  • Sedating antihistamines: may enhance drowsiness.
  • Alcohol: can increase central nervous system effects.
  • Bronchodilators: monitor for any change in cough relief efficacy.
  • Certain antibiotics (e.g., macrolides): observe for possible pharmacokinetic changes.

Frequently Asked Questions

Levotuss contains levodropropizine, an oral antitussive indicated for the symptomatic relief of dry and non‑productive coughs, helping to reduce the frequency and intensity of coughing episodes.

Levodropropizine acts peripherally by inhibiting the release of sensory neuropeptides such as substance P from airway afferent nerves, which lowers the sensitivity of cough receptors and diminishes the cough reflex without affecting the central nervous system.

The appropriate dose of Levotuss is determined by the prescribing healthcare professional based on the patient’s age, weight, and clinical condition. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for levodropropizine in pregnancy and lactation are limited. It should be used only if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

To order Levotuss, submit an enquiry on the product page at gnhindia.com with 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.

Unlike codeine, which is a centrally acting opioid cough suppressant, levodropropizine works peripherally and does not produce opioid‑related side effects such as respiratory depression. It is generally better tolerated for patients who need a non‑opioid option.

Store Levotuss at room temperature, below 25 °C, in the original packaging. Protect it from moisture, direct sunlight, and extreme temperatures to maintain product stability.

Levotuss is taken orally. The tablet or liquid should be swallowed with a glass of water, following the dosage instructions provided by the prescriber. It can be taken with or without food.

Serious adverse reactions, although rare, include allergic responses such as rash, urticaria, angioedema, and anaphylaxis, as well as hepatic enzyme elevations and neutropenia. Any signs of severe hypersensitivity or liver dysfunction should prompt immediate medical attention.

Levotuss should be avoided by individuals with known hypersensitivity to levodropropizine or any of its excipients, patients with severe hepatic impairment unless supervised, and children below the age limit specified by the prescriber. Caution is also advised for pregnant or breastfeeding women.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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