Product image of Lidoject (Lidocaine Hydrochloride) supplied by GNH India

Lidoject

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Lidoject (Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Lidoject, is a local anesthetic presented as a topical preparation for skin and mucous membrane use. It provides reversible nerve impulse blockade to relieve pain during minor skin procedures, superficial wound care, and mucosal irritation in adult patients. The formulation is intended for external application and is commonly employed in clinical settings to achieve rapid, localized numbness without systemic effects.

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

Manufacturer / TM Owner

Labesfal Laboratorios Almiro, S.A.

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Indications & Clinical Uses

  • Lidoject, a topical local anesthetic, is used to provide surface anesthesia in several clinical situations.
  • Minor skin procedures: provides localized numbness to facilitate biopsies, suturing or minor excisions.
  • Superficial wound or irritation: relieves pain from cuts, abrasions or irritant contact.
  • Mucous membranes: anesthetizes oral or nasal mucosa prior to minor interventions.

How It Works

  • Lidoject contains lidocaine hydrochloride, which reversibly blocks voltage‑gated sodium channels on neuronal membranes. By inhibiting sodium influx, it prevents depolarization and propagation of nerve impulses, resulting in a temporary loss of sensation in the applied area without affecting surrounding tissues.

Side Effects

Lidoject may cause local or systemic adverse reactions following topical application.

Common Side Effects

  • Transient burning or stinging at the application site
  • Mild erythema or redness
  • Pruritus or itching
  • Localized swelling
  • Dryness of the skin or mucosa
  • Temporary tingling sensation

Serious or Rare Side Effects

  • Allergic contact dermatitis
  • Systemic toxicity presenting as dizziness, tinnitus, or seizures
  • Cardiac arrhythmia or conduction disturbances
  • Severe local tissue necrosis
  • Anaphylactic reaction
  • Methemoglobinemia (rare)

Precautions & Warnings

  • When using Lidoject, consider the following safety measures.
  • Allergy assessment: avoid use in patients with known lidocaine hypersensitivity.
  • Application area: limit to intact skin or mucosa; do not apply to large surface areas.
  • Concurrent anesthetics: avoid combining with other topical anesthetics to prevent cumulative toxicity.
  • Medical conditions: use cautiously in patients with cardiac conduction disorders or severe liver disease.
  • Pregnancy and lactation: consult a healthcare professional before use.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lidoject can interact with other medications; monitor patients accordingly.

Major Interactions (Avoid)

  • Other amide‑type local anesthetics: may increase systemic toxicity.
  • Class I antiarrhythmic drugs (e.g., quinidine, procainamide): can potentiate cardiac effects.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may raise lidocaine plasma levels.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may enhance lidocaine's bradycardic effect.
  • Diuretics (e.g., furosemide): may affect plasma protein binding and increase free drug concentration.

Frequently Asked Questions

Lidoject is a topical formulation of lidocaine hydrochloride used to provide local anesthesia for minor skin procedures, to relieve pain from superficial wounds or irritations, and to numb mucous membranes before minor interventions.

Lidocaine hydrochloride blocks voltage‑gated sodium channels on peripheral nerves, preventing the influx of sodium ions required for depolarisation. This inhibition stops nerve impulse transmission, producing a reversible loss of sensation in the area where the product is applied.

The appropriate amount of Lidoject is determined by the prescribing healthcare professional based on the size of the area to be anesthetized, the specific procedure, and patient factors. No fixed dosing regimen is provided here.

Safety data for Lidoject in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits against any possible risks before prescribing it to pregnant or nursing individuals.

To request Lidoject, 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.

Lidoject contains lidocaine, an amide‑type local anesthetic known for rapid onset and moderate duration. Compared with ester‑type agents such as benzocaine, lidocaine generally has a lower risk of allergic reactions and provides more consistent depth of anesthesia for minor procedures.

Lidoject should be stored at room temperature, below 25 °C, in its original packaging. Protect it from moisture, direct sunlight and extreme temperatures to maintain product stability.

Lidoject is applied topically to the intended skin or mucosal area. The surface should be clean and dry; a thin layer is spread evenly and allowed to act for the time recommended by the prescriber before the procedure begins.

Serious adverse events, although rare, include systemic toxicity such as central nervous system symptoms (e.g., seizures), cardiac arrhythmias, severe allergic reactions, and local tissue necrosis. Prompt medical attention is required if any of these occur.

Lidoject should be avoided in individuals with a known hypersensitivity to lidocaine or other amide‑type local anesthetics, in patients with significant cardiac conduction disorders, and in those with severe liver impairment unless specifically directed by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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