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

Lidocaina Aguettant

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Lidocaina Aguettant (Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Lidocaina Aguettant, is a local anesthetic presented as a sterile solution for infiltration, intradermal and intravenous use. It provides rapid, reversible loss of sensation in targeted tissues and is employed to facilitate minor surgical, dental, dermatologic and regional anesthesia procedures.

GNH India supplies Lidocaina Aguettant as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU GMP standards and provides reliable logistics to meet global regulatory requirements.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

  • Lidocaine Hydrochloride is used as a local anesthetic for procedures requiring temporary nerve block.
  • Minor surgical procedures: provides rapid loss of sensation to facilitate incision, excision or suturing with minimal discomfort.
  • Dental procedures: numbs oral tissues to allow tooth extraction, cavity preparation or periodontal surgery without pain.
  • Dermatologic procedures: anesthetizes skin for biopsies, excisions or laser treatments, improving patient tolerance.
  • Intravenous regional anesthesia: blocks limb nerves when administered with a tourniquet, enabling surgery on the extremity without systemic analgesia.

How It Works

  • Lidocaine Hydrochloride exerts its effect by binding to the intracellular portion of voltage‑gated sodium channels in neuronal membranes. This binding stabilizes the channel in an inactivated state, preventing the influx of sodium ions during depolarization. Consequently, the generation and propagation of action potentials are inhibited, leading to a reversible loss of sensory and, at higher concentrations, motor nerve conduction in the administered area.

Side Effects

Lidocaine Hydrochloride may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Transient burning or stinging at the injection site
  • Mild dizziness or light‑headedness
  • Nausea or vomiting
  • Localized swelling or erythema

Serious or Rare Side Effects

  • Systemic toxicity presenting as seizures or cardiac arrhythmias
  • Severe allergic reactions including anaphylaxis
  • Methemoglobinemia causing cyanosis
  • Persistent numbness or motor weakness beyond the expected duration

Precautions & Warnings

  • When using Lidocaina Aguettant, several precautions should be observed to ensure patient safety and product integrity.
  • Allergy assessment: verify no known hypersensitivity to amide‑type local anesthetics
  • Dose calculation: base total dose on patient weight and maximum recommended limits
  • Cardiac monitoring: observe for signs of arrhythmia in patients with pre‑existing heart disease
  • Use with caution in hepatic impairment: reduced metabolism may increase systemic exposure
  • Avoid intravascular injection: aspirate before administration to prevent rapid systemic absorption
  • Store at ambient temperature: keep below 25°C, protect from moisture and light in the original packaging

Avoid Interactions

Lidocaine Hydrochloride can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Class I antiarrhythmics (e.g., quinidine, procainamide): may potentiate cardiotoxic effects
  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): increase plasma lidocaine concentrations

Moderate Interactions (Monitor Closely)

  • Beta‑blockers (e.g., propranolol): may enhance bradycardia when combined with lidocaine
  • Other local anesthetics: cumulative dosing can raise risk of systemic toxicity
  • Diuretics (e.g., furosemide): may reduce plasma protein binding, modestly increasing free lidocaine

Frequently Asked Questions

Lidocaina Aguettant contains lidocaine hydrochloride and is employed to provide local anesthesia for minor surgical, dental, dermatologic and intravenous regional procedures. By temporarily blocking nerve conduction, it allows clinicians to perform interventions with reduced pain and patient discomfort.

Lidocaine blocks voltage‑gated sodium channels on neuronal membranes, stabilizing them in an inactive state. This prevents sodium influx during depolarisation, inhibiting the generation and propagation of nerve impulses and resulting in a reversible loss of sensation in the treated area.

The appropriate dose of Lidocaina Aguettant is determined by the prescribing clinician based on the specific procedure, patient weight, age, and overall health. Only a qualified health professional should calculate and administer the exact amount required.

Safety data for lidocaine hydrochloride in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. Use during pregnancy or while breastfeeding should only occur when the potential benefit justifies any potential risk, as assessed by the prescriber.

To request Lidocaina Aguettant, 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 any cold‑chain needs) and the necessary import documentation.

Lidocaine is an amide‑type local anesthetic with a rapid onset and moderate duration, making it suitable for many outpatient procedures. Compared with bupivacaine, which has a longer duration but slower onset, lidocaine offers quicker pain relief but may require repeat dosing for prolonged surgeries. Choice depends on procedural length and desired recovery time.

Lidocaina Aguettant should be stored at ambient temperature, preferably below 25 °C, in its original container to protect it from moisture and light. Ensure the vial or ampoule remains sealed until use, and discard any product that appears discoloured or contains particles.

The product is supplied as a sterile solution for injection and can be given by infiltration, intradermal injection, or intravenous regional (Bier) block. Administration techniques follow standard aseptic procedures, and the clinician should aspirate before injection to avoid inadvertent intravascular delivery.

Serious adverse events include systemic toxicity that may manifest as seizures, cardiac arrhythmias, or cardiovascular collapse, as well as severe allergic reactions such as anaphylaxis. Prompt recognition and supportive treatment are essential if signs of toxicity appear.

Patients with a known hypersensitivity to lidocaine or other amide‑type local anesthetics, those with severe hepatic impairment, and individuals with certain cardiac conduction disorders should avoid using Lidocaina Aguettant unless a specialist determines that benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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