Product image of Lidokain Aguettant (Lidocaine Hydrochloride) supplied by GNH India

Lidokain Aguettant

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Lidokain Aguettant (Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Lidokain Aguettant, is a local anesthetic presented as a sterile solution for infiltration, intradermal and subcutaneous use. It provides rapid, reversible loss of sensation in targeted tissues for minor procedures.

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

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Lidocaine Hydrochloride is used to provide local anesthesia in various procedural settings.

  • Minor surgical procedures: rapid onset anesthesia to facilitate incision and excision.
  • Dental procedures: numbs oral tissues for extractions, restorations and periodontal work.
  • Dermatologic procedures: anesthetizes skin for biopsies, excisions, laser treatments and cosmetic interventions.

How It Works

  • Lidocaine Hydrochloride blocks voltage‑gated sodium channels on neuronal membranes, preventing the initiation and propagation of action potentials. By stabilizing the neuronal membrane, it inhibits nerve impulse transmission, resulting in a reversible loss of sensation in the area where it is administered.

Side Effects

Lidocaine Hydrochloride may cause adverse reactions at the injection site or systemically.

Common Side Effects

  • Burning or stinging sensation at the injection site.
  • Mild redness or swelling of the treated area.
  • Dizziness or light‑headedness.

Serious or Rare Side Effects

  • Anaphylactic reaction (severe allergy).
  • Cardiac arrhythmias, including ventricular tachycardia.
  • Central nervous system toxicity such as seizures or loss of consciousness.

Precautions & Warnings

When using Lidokain Aguettant, consider the following precautions:

  • Allergy assessment: verify no known hypersensitivity to lidocaine or amide‑type anesthetics.
  • Dose limitation: employ the lowest effective amount to stay within recommended maximum dose.
  • Cardiac monitoring: observe patients with pre‑existing heart disease for arrhythmias.
  • Aspiration before injection: avoid inadvertent intravascular administration.
  • Pregnancy and lactation: use only if the clinical benefit outweighs potential risk.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Lidokain Aguettant can interact with other medications; awareness of the interaction level is essential.

Major Interactions (Avoid)

  • Class I antiarrhythmic agents (e.g., quinidine, procainamide): increase systemic toxicity.
  • Beta‑blockers (e.g., propranolol): may potentiate cardiac depressant effects.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): can raise plasma lidocaine concentrations.

Moderate Interactions (Monitor Closely)

  • Concurrent use of other local anesthetics: cumulative toxicity risk.
  • Diuretics (e.g., furosemide): may reduce plasma protein binding, enhancing free drug levels.
  • General anesthetics (e.g., propofol): additive central nervous system depression.

Frequently Asked Questions

Lidokain Aguettant is a sterile lidocaine hydrochloride solution used to provide local anesthesia for minor surgical, dental and dermatologic procedures. It temporarily blocks nerve conduction in the targeted area, allowing clinicians to perform interventions without pain.

Lidocaine hydrochloride blocks voltage‑gated sodium channels on nerve membranes, preventing the initiation and propagation of action potentials. This inhibition stops nerve signals from reaching the brain, producing a reversible loss of sensation in the area where it is administered.

The dose of Lidokain Aguettant is determined by the prescribing clinician based on the type of procedure, the size of the treatment area, patient weight and overall health. Only a qualified healthcare professional should calculate and administer the appropriate amount.

Safety data for lidocaine hydrochloride in pregnancy and lactation are limited. It should be used only when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under the guidance of a qualified healthcare provider.

To order, 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 if needed) and required import documentation.

Lidocaine offers a rapid onset (1–3 minutes) and moderate duration (30–120 minutes), making it suitable for short procedures. Compared with longer‑acting agents such as bupivacaine, lidocaine provides quicker recovery but a shorter analgesic window, which can be advantageous when fast return of sensation is desired.

Store the product at ambient temperature, preferably below 25 °C, in its original sealed container. Protect it from direct sunlight, moisture and extreme temperatures to maintain sterility and potency.

The solution is administered by infiltration, intradermal or subcutaneous injection. The clinician injects the drug directly into the tissue surrounding the target area, often after aspirating to ensure the needle is not within a blood vessel.

Serious risks include severe allergic reactions (anaphylaxis), cardiac arrhythmias such as ventricular tachycardia, and central nervous system toxicity that can lead to seizures or loss of consciousness. Immediate medical attention is required if any of these symptoms occur.

Patients with a known hypersensitivity to lidocaine or other amide‑type local anesthetics, those with severe heart block, uncontrolled arrhythmias, or certain metabolic disorders should avoid using this product. The prescribing clinician must assess each patient’s medical history before administration.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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