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

Lidocaine Laboratoire Aguettant

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Lidocaine Laboratoire Aguettant (Lidocaine Hydrochloride)

Lidocaine, the active ingredient in Lidocaine Laboratoire Aguettant, is a local anesthetic presented as a sterile solution for infiltration, intradermal and intravenous use. It provides rapid, reversible loss of sensation for minor surgical procedures and can be used intravenously for antiarrhythmic therapy.

GNH India supplies Lidocaine Laboratoire 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 acts on peripheral nerves and cardiac tissue to produce anesthesia or antiarrhythmic effects.

  • Minor surgical procedures: provides local anesthesia to numb the targeted area.
  • Infiltration anesthesia: creates a field block for soft‑tissue interventions.
  • Intradermal anesthesia: numbs superficial skin layers for diagnostic or therapeutic procedures.
  • Intravenous antiarrhythmic therapy: stabilises cardiac membranes to treat ventricular arrhythmias.

How It Works

  • Lidocaine blocks voltage‑gated sodium channels on neuronal and cardiac membranes, preventing the rapid influx of sodium ions required for depolarisation. This inhibition halts the propagation of nerve impulses and stabilises cardiac myocytes, reducing ectopic electrical activity and producing local anaesthesia as well as antiarrhythmic effects.

Side Effects

Lidocaine may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Burning or stinging at the injection site
  • Tingling or numbness in the treated area
  • Light‑headedness or dizziness
  • Nausea or mild vomiting
  • Transient hypotension
  • Local swelling or erythema

Serious or Rare Side Effects

  • Allergic reactions such as rash, urticaria or anaphylaxis
  • Severe hypotension or cardiovascular collapse
  • Cardiac arrhythmias including ventricular tachycardia
  • Central nervous system toxicity (seizures, confusion)
  • Methemoglobinemia
  • Respiratory depression

Precautions & Warnings

Lidocaine should be used with careful clinical assessment and monitoring.

  • Hypersensitivity: avoid in patients with known lidocaine allergy.
  • Cardiac conduction disorders: use cautiously in patients with heart block or severe ventricular dysfunction.
  • Hepatic impairment: dose may need adjustment as lidocaine is metabolised in the liver.
  • Renal disease: monitor plasma levels in severe renal failure.
  • Pregnancy and lactation: safety not established; weigh benefits against potential risks.
  • Store below 25°C: keep in original container, protect from light and moisture.

Avoid Interactions

Lidocaine can interact with several drug classes, altering its safety profile.

Major Interactions (Avoid)

  • Class I antiarrhythmics (e.g., quinidine, procainamide): may increase lidocaine toxicity.
  • Central nervous system depressants (e.g., barbiturates, opioids): additive CNS depression.
  • Beta‑adrenergic blockers (e.g., propranolol): may enhance cardiac effects.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., erythromycin, clarithromycin): may raise plasma lidocaine levels.
  • Diuretics (e.g., furosemide): can reduce plasma protein binding, increasing free drug.
  • Concurrent local anesthetics: risk of cumulative systemic toxicity.

Frequently Asked Questions

Lidocaine Laboratoire Aguettant is a sterile solution containing lidocaine hydrochloride. It is used to provide local anesthesia for minor surgical procedures, infiltration and intradermal anesthesia, and as an intravenous antiarrhythmic agent to treat certain cardiac arrhythmias.

Lidocaine blocks voltage‑gated sodium channels on nerve and cardiac cell membranes. By preventing sodium influx, it stops the generation and propagation of action potentials, resulting in loss of sensation in the treated area and stabilisation of cardiac electrical activity.

The appropriate dose is determined by the prescribing clinician based on the intended indication, patient characteristics, and route of administration. Dosage regimens are not standardised and must follow the prescriber’s orders and local guidelines.

Safety data for lidocaine in pregnancy and lactation are limited. The product should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision should be made by the treating physician.

Enquiries are submitted via the product page on gnhindia.com, where you specify 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 any cold‑chain requirements) and necessary import documentation.

Lidocaine is a medium‑duration amide‑type local anesthetic, offering rapid onset and a favourable safety profile compared with longer‑acting agents like bupivacaine. It is less lipid‑soluble than some alternatives, which can result in a slightly shorter duration of action but also lower risk of cardiotoxicity at therapeutic doses.

Lidocaine Laboratoire Aguettant should be stored below 25 °C, in its original packaging, protected from light and moisture. Do not freeze the solution, and keep it out of reach of children.

The product is supplied as a sterile solution for injection. It can be administered by infiltration, intradermal injection, or intravenous infusion, depending on the clinical indication and the prescriber’s instructions.

Serious risks include severe allergic reactions, cardiovascular collapse, profound hypotension, life‑threatening arrhythmias, central nervous system toxicity such as seizures, and methemoglobinemia. Prompt recognition and supportive management are essential if these events occur.

Patients with a known hypersensitivity to lidocaine or other amide‑type local anesthetics should avoid this product. It is also contraindicated in individuals with severe heart block, significant ventricular dysfunction, or in those where the risk of systemic toxicity outweighs the therapeutic benefit.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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